Dermatopathology Primer of Cutaneous Tumor

Dermatopathology
Primer of Cutaneous Tumors
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Dermatopathology
Primer of Cutaneous Tumors
Omar P. Sangueza, MD Parisa Mansoori, MD

Visiting Fellow in Dermatopathology
Professor of Dermatology Wake Forest University School of Medicine
and Pathology Winston-Salem, North Carolina, USA
Director of Dermatopathology
Saleha A. Aldawsari, MD
Wake Forest University Visiting Fellow in Dermatopathology
Health Sciences Department of Pathology
Winston-Salem, North Carolina, Wake Forest University School of Medicine
USA Winston-Salem, North Carolina, USA
Amir Al-Dabagh, MD
Visiting Fellow in Dermatology
Department of Dermatology
Wake Forest University School of Medicine
Sara Moradi Tuchayi, MD, MPH Winston-Salem, North Carolina, USA
Research Fellow
Department of Dermatology Amany A Fathaddin, MD
Wake Forest University School of Medicine Visiting Fellow in Dermatopathology
Winston-Salem, North Carolina, Wake Forest University School of Medicine
USA Winston-Salem, North Carolina, USA
Steven R. Feldman, MD, PhD
Professor of Dermatology and Pathology
Wake Forest University Health Sciences
Winston-Salem, North Carolina, USA
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CRC Press
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Contents 3.1.4 Pilar sheath acanthoma
3.1.5 Tumor of the follicular
37
Acknowledgements 7 infundibulum 38
Introduction 9 3.2 Sebaceous tumors
1 Tumors of the Epidermis 3.2.1 Benign neoplasms
1.1 Benign tumors 3.2.1.1 Sebaceous hyperplasia 39
1.1.1 Epidermal proliferations 3.2.1.2 Sebaceoma 40
1.1.1.1 Epidermal nevus 10 3.2.1.3 Sebaceous adenoma 41
1.1.1.2 Clear cell acanthoma 11 3.2.2 Malignant tumors
1.1.2 Warts and variants 3.2.2.1 Sebaceous carcinoma 42
1.1.2.1 Viral warts 12 3.3 Sweat gland neoplasms
1.1.2.2 Trichilemmoma 13 3.3.1 Benign neoplasms
1.1.2.3 Inverted follicular keratosis 14 3.3.1.1 Apocrine adenoma 43
1.1.2.4 Solar lentigo 15 3.3.1.2 Syringocystadenoma
1.1.2.5 Seborrheic keratosis 16 papilliferum 44
1.1.2.6 Warty dyskeratoma 17 3.3.1.3 Hidradenoma 45
1.2 Malignant tumors 3.3.1.4 Cylindroma 46
1.2.1 Basal cell carcinoma and variants 3.3.1.5 Apocrine hidrocystoma 47
1.2.1.1 Basal cell carcinoma and 3.3.1.6 Mixed tumor 48
variants 18 3.3.1.7 Spiradenoma 49
1.2.2 Squamous cell carcinoma and 3.3.1.8 Syringoma 50
variants 3.3.1.9 Poroma 51
1.2.2.1 Bowen’s disease 20 3.3.2 Malignant tumors
1.2.2.2 Keratoacanthoma 21 3.3.2.1 Adenoid cystic carcinoma 52
1.2.2.3 Squamous cell carcinoma 22 3.3.2.2 Microcystic adnexal carcinoma 53
3.3.2.3 Extramammary Paget’s disease 54
2 Melanocytic Neoplasms 3.3.2.4 Hidradenocarcinoma 55
2.1 Benign neoplasms 3.3.2.5 Porocarcinoma 56
2.1.1 Lentigo simplex 24
2.1.2 Melanocytic nevi 25 4 Tumors of Fibrous Tissue
2.1.3 Halo nevus 26 4.1 Benign tumors
2.1.4 Spitz nevus 27 4.1.1 Nodular fasciitis 57
2.1.5 Blue nevus 28 4.1.2 Dermatofibroma 58
2.2 Malignant lesions 4.1.3 Superficial fibromatosis 59
2.2.1 Malignant melanoma and variants 31 4.2 Malignant tumors
4.2.1 Fibrosarcomas 60
3 Tumors of Cutaneous Appendages 4.2.2 Dermatofibrosarcoma
3.1 Hair follicle tumors protuberans 61
3.1.1 Trichoepithelioma 33 4.2.3 Atypical fibroxanthoma 62
3.1.2 Trichoblastoma 35
3.1.3 Trichofolliculoma 36
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5 Tumors of Fat 9 Cutaneous Cysts
5.1 Lipoma 63 9.1 Epidermoid cyst 91
5.2 Angiolipoma 64 9.2 Pilar cyst 92
5.3 Nevus lipomatosus superficialis 65 9.3 Dermoid cyst 93
9.4 Steatocystoma 94
6 Tumors of Smooth Muscle
9.5 Bronchogenic cyst 95
6.1 Benign neoplasms
9.6 Cutaneous ciliated cyst 96
6.1.1 Leiomyoma 66
9.4 Median raphe cyst 97
6.2 Malignant tumors
6.2.1 Leiomyosarcoma 67 10 Cutaneous Metastases
10.1 Cutaneous metastases 98
7 Neural Tumors
7.1 Nerve sheath tumors 11 Cutaneous Infiltrates: Non Lymphoid
7.1.1 Neurofibroma 68 11.1 Mast cell infiltrates
7.1.2 Schwannoma 69 11.1.1 Mastocytosis 100
7.1.3 Perineurioma 71 11.2 Histiocytic infiltrates
7.1.4 Palisaded and encapsulated 11.2.1 Juvenile xanthogranuloma 102
neuromas 72 11.2.2 Xanthomas 103
7.1.5 Cutaneous ganglioneuroma 73 11.2.3 Langerhans cell histiocytosis 104
7.1.6 Nasal glioma 74 11.3 Neuroendocrine infiltrates
7.1.7 Cutaneous meningioma 75 11.3.1 Merkel cell carcinoma 105
7.1.8 Granular cell tumor 76
12 Cutaneous Infiltrates: Lymphoid and
8 Vascular Tumors Leukemic
8.1 Hyperplasias 12.1 Pseudolymphomas
8.1.1 Pyogenic granuloma 77 12.1.1 Cutaneous pseudolymphomas 106
8.2 Benign neoplasms 12.2 Cutaneous lymphomas
8.2.1 Infantile hemangiomas 78 12.2.1 T-cell lymphomas 107
8.2.2 Cherry angiomas 79 12.2.2 Primary cutaneous CD30+ T-cell
8.2.3 Arteriovenous hemangioma 80 lymphoproliferative disorders 109
8.2.4 Microvenular hemangioma 81 12.2.3 B-cell lymphomas 110
8.2.5 Tufted angioma 82 12.3 Leukemic and miscellaneous infiltrates
8.2.6 Glomeruloid hemangioma 84 12.3.1 Leukemia cutis 111
8.2.7 Acquired elastotic hemangioma 85
References 112
8.2.8 Kaposiform hemangioendothelioma 86
Glossary of Terms 121
8.2.9 Glomus tumor and glomangioma 87
8.3 Malignant tumors
8.3.1 Kaposi sarcoma 88
8.3.2 Angiosarcoma 90
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Acknowledgements
The second volume of Dermatopathology Primer is a complement to the first volume on
inflammatory disease. This volume was produced in collaboration with many of the
international fellows of the Section of Dermatopathology of the Wake Forest University
School of Medicine.
We want to thank especially Professor Luis Requena from the Department of Dermatology
of the Universidad Autonoma de Madrid for allowing us to use some of his wonderful
material.
We also thank Mr. Charles P. Sangueza for his help in editing and critically reviewing many
chapters of this manuscript.
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Introduction
The second volume of the Dermatopathology Primer series deals with neoplastic diseases of
the skin. This volume is a complement the first volume on inflammatory diseases.
As we noted in the first volume, the intent of these books is to introduce the basic
concepts of dermatopathology to medical students and residents training in pathology and
dermatology.
The book is organized into chapters discussing the differentiation of various neoplasms.
These include cysts, epidermal, melanocytic lymphoid, and soft tissue neoplasms, both
benign and malignant. For each neoplasm we have used illustrations and discussion
demonstrating the most characteristic features. In addition, we have also included
illustrations of the entities that enter in the differential diagnosis. Because of space
limitations and the limited scope of the book, variations of the different neoplasms are not
included. For further information the reader is encourage to consult any of several standard
books of dermatopathology.
We hope that this book will fulfill the expectations of students beginning the study of
dermatopathology.
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TUMORS OF THE EPIDERMIS
Benign Tumors • Epidermal proliferations
Epidemiology Epidermal nevus
• Occurs in 1 in 1000
live births Introduction
• 80% of lesions appear Epidermal nevus is a term that encompasses hamartomatous proliferations
within the first year of of epithelium that originate from embryonal ectoderm. They are classified on
life, with the majority the basis of the main histologic component: keratinocytes (epidermal nevus),
of lesions appearing sebaceous gland (nevus sebaceous), pilosebaceous unit (nevus comedonicus),
by age 14. There are eccrine gland (eccrine nevus), or apocrine gland (apocrine nevus).
rare reports of epidermal nevi appearing
in adults
• Mostly sporadic, however, some familial
Histological
cases have been documented Features 2
Pathophysiology 1. Acanthosis
2. Papillomatosis
1
• Genetic mosaicism is thought to be the 3. Hyperkeratosis

underlying cause, likely a postzygotic 4. Hyperpigmentation of the 4
somatic mutation basal layer may be seen
• The mutation affects pluripotential cells giv- 5. Thickening of the granular
ing rise to hamartomas of different cell lines layer
Special Studies
• Extensive epidermal nevi require further 3
work up. These patients require a complete
examination, including the eyes, in order to 5
rule out cataracts and optic nerve hypoplasia;
and neuroimaging and cardiac studies to rule
out aneurysms and patent ductus arteriosus
Clinical Features
Epidermal Nevus
• The characteristic epidermal nevus presents
as a linear, hyperpigmented, papillomatous
plaque that can vary from pink to black,
velvety to verrucous, flat to thick, and can
Histological
involve small or extensive areas of the skin Differential
• The lesions are usually asymptomatic 1. Seborrheic keratosis:
• The inflammatory linear verrucous • Well-circumscribed
epidermal nevi (ILVEN) variant is pruritic neoplasm composed of
and may be erythematous or scaly basaloid cells
• The lesions are more common on the trunk • Basket weave orthokeratosis
or extremities along the Blaschko lines, but • Horn pseudocysts
may also occur on the face and neck
• Approximately one-third of the patients
develop the so-called epidermal nevus Seborrheic Keratosis
syndrome (ENS), an entity in where there
is involvement of other systems including Important Things To Know
the nervous, cardiovascular, urogenital,
and/or skeletal • Neoplasms such as basal cell carcinoma (BCC), squamous cell
carcinoma (SCC) and keratoacanthoma are not usually associated with
epidermal nevi
Clinical Variants • Malignancy in epidermal nevus, when it does occur, develops after
• The inflammatory linear verrucous epi- puberty
dermal nevi (ILVEN)
• Epidermal nevus syndrome (ENS) 10
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Clear cell acanthoma (Degos
acanthoma, pale cell acanthoma)
Introduction
Clear cell acanthoma (CCA) is a benign epidermal neoplasm composed of
keratinocytes with ample pale cytoplasm and centrally placed nuclei. It consists Epidemiology
Epidemiology
of a well-demarcated, solitary, shiny, and brown to orange papule or nodule. • Middle-aged; mostly after the age of 40
•
Histological features • Male-to-female ratio is 1:1
1. Well-circumscribed lesions composed of uniform pale keratinocytes Pathophysiology

2. Distinct transition between the normal epidermis and the paler cells
• It is unclear whether CCA is a
3. Parakeratosis with variable number of neutrophils
true neoplasm or an inflammatory
4. Neutrophils are scattered within the acanthoma
dermatosis
5. Absence of granular layer and epidermal melanin
6. Suprapapillary plate thinning, sparing of adnexal epidermis and dilated
tortuous dermal blood vessels in the papillary dermis
Clinical features
• Solitary, slow-growing, well-
demarcated, erythematous to brown
3
5 papule or nodule with moist eroded
6 surface. In some cases a collarette
1
of scale is present and produces a
psoriasiform appearance
4
• The lesions are asymptomatic and slow
2
growing
• Affects most commonly the legs, but
it can be also seen on the thigh, face,
Clear cell acanthoma forearm, trunk, and inguinal region
• Almost completely blanches with
pressure
Histological differential • Size: 0.3–2 cm (giant clear cell
acanthoma >5 cm)
1. Psoriasis vulgaris: 2. Trichilemmoma:
• No clear cells with distinct
transition between the normal
• Neutrophils absent
• Outlined by a thick eosinophilic
Special studies
epidermis and the clearer/paler basement membrane • Keratinocytes in the epidermis are
cells in the epidermis • Peripheral palisading glycogen rich and stain with periodic
• Numerous squamous eddies acid-Schiff, diastase labile
Important things to know

• The clinical features can be confused with pyogenic granuloma and
seborrheic keratosis
Clinical Variants
• None
11
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Benign Tumors • Warts and variants
Viral warts (verrucae)
Introduction
Verrucae are lesions caused by human papillomavirus (HPV), which produces
various types of warts on different parts of the skin.
Epidemiology Histological features

1. Exophytic neoplasm with finger-like projections; compact hyperkeratosis,
• Verruca occurs predominantly in papillomatosis, hypergranulosis and acanthosis; inward turning of the
children and adolescents although adults elongated rete ridges at the edge of the lesion
are also frequently affected 2. Parakeratosis at the tips of the projections
3. Dilated blood vessels in papillary dermis
Pathophysiology 4. Large vacuolated cells with small pyknotic nucleus (koilocytes)
• Most verrucae vulgaris are induced • Flat warts or verruca plana show prominent hypergranulosis. The cytoplasm
by HPV-2. Palmoplantar warts are of the cells shows blue-gray inclusions
associated with HPV-1 or HPV-4 • Palmoplantar warts or myrmecia warts show red cytoplasmic inclusions
infection. Verruca plana is associated • Epidermodysplasia verruciformis characterized by large cells with
with HPV-3 and HPV-10 conspicuous perinuclear halo. The cytoplasm, which is blue-gray, contains
• Epidermodysplasia verruciformis is a rare keratohyalin granules
autosomal recessive genodermatosis due
to mutation EVER1/TMC6 or EVER2/
TMC8 genes. Warts induced by different
2
types of HPV 1
• In condylomas, HPV-6 and 11 are most 3
commonly identified and are sexually 4
transmitted
Clinical features Wart 2

• Verruca vulgaris are hard papules found on Wart 3
exposed parts; mostly on the fingers
• Palmoplantar warts are found on the
palm or the sole and they are painful
• Verrucae plana are multiple skin-colored
or slightly elevated papules on face and
Histological Differential
extremities • Seborrheic keratosis: horn pseudocysts are seen and basket weave stratum
• Condylomas are fleshy exophytic lesion corneum are seen
of the anogenital region • Squamous cell carcinoma: atypical pleomorphic cells with mitoses are seen
Special studies
• In situ hybridization and
immunohistochemistry to subtype HPVs
Seborrheic keratosis Verrucous squamous cell carcinoma

Clinical Variants
Important Things To Know
Clinical Variants • Patients with epidermodysplasia verruciformis show numerous flat
• Flat warts (verruca plana) warts
• Palmoplantar warts (myrmecia warts)
• Condyloma
12
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Trichilemmoma (tricholemmoma)
Introduction
Trichilemmoma (tricholemmoma) is a form of benign adnexal neoplasm with
differentiation mostly toward the follicular outer root sheath. These lesions
are variants of warts and recently it has been demonstrated the presence of
papillomavirus DNA in these lesions. Epidemiology
• The majority of trichilemmoma occur
Histological features between the age of 20 and 80 years, with
1. Small circumscribed and lobular or multilobular proliferation of pale a mean age of 30 years
keratinocytes • Male-to-female ratio is approximately 1:1
2. Peripheral palisading of the nuclei • Trichilemmoma are not associated with
3. Outlined by a thick densely eosinophilic basement membrane morbidity or mortality
4. Numerous squamous eddies
Pathophysiology
• Trichilemmomas are induced by HPV
• A mutation in the tumor suppressor gene
PTEN/MMAC1, as observed in Cowden
syndrome, may play a causative role
2
3 Clinical features
4 • Trichilemmomas appear as simple or
1
2 multiple small (3–8 mm in diameter)
papules or nodules
• Individual lesions may be keratotic or
smooth-surfaced and coloration usually
matches that of surrounding skin
Trichilemmoma • Predominantly located on the central face,
particularly around the nose and upper lip,
Histological differential but may occur at any non-glabrous site
• Most lesions are clinically misdiagnosed
1. Clear cell acanthoma: as BCC or benign keratosis
• Glycogenated pale segment of epidermis is sharply demarcated from the • Multiple trichilemmomas typically present
surrounding skin on the facial or genital skin. On genital
• Neutrophils are noted throughout the lesion and in the overlying crust skin they simulate the clinical pattern of a
• Absence of thickening of the basement membrane zone condyloma, especially if multiple
• Multiple trichilemmomas can be
associated with Cowden syndrome
(an autosomal dominant condition
distinguished by multiple trichilemmoma,
sclerotic fibromas, acrokeratosis and
adenocarcinoma of the breast, thyroid
gland, or gastrointestinal tract)
Special studies
• Hematoxylin and eosin is the stain of choice
• PAS-D (periodic acid-Schiff with diastase)
stain may be used to highlight the
Clear cell acanthoma thickened basement membrane
• A CD34 stain may be used to
differentiate between a desmoplastic
trichilemmoma and a BCC (CD34 positive
Important Things To Know in desmoplastic trichilemmoma and
• Desmoplastic trichilemmoma is characterized by irregular extensions negative in BCC)
of the outer root sheath which project into sclerotic collagen bundles
and may simulate infiltrating squamous cell carcinoma
Clinical Variants
• None
13
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Inverted follicular keratosis
Introduction
Inverted Follicular Keratosis (IFK) is an uncommon benign tumor of the
follicular infundibulum that can be confused, both clinically and histologically,
with several benign and malignant skin conditions. The lesion typically appears
Epidemiology on the face as a solitary firm papule and is characterized histologically by an
endophytic proliferation of keratinocytes with the formation of squamous eddies.
• Middle-aged to elderly individuals
• Male-to-female ratio is 2:1 Histological features
Pathophysiology 1. Endophytic proliferation of follicular keratinocytes extending downward into
the dermis in a well-demarcated, lobular configuration
• The involved cells are thought to arise 2. Hyperkeratosis, parakeratosis and occasionally papillomatosis
from the follicular infundibulum, 3. Squamous eddies
although the reason for proliferation is 4. Mild inflammatory cell infiltrate, predominantly lymphohistiocytic is common
unknown in dermis
Clinical features
• Solitary, flesh-colored or pink, firm
papule which measures from 0.3–1 cm
in diameter
1
• Most commonly found on face 2
4 3
(predilection for cheek, upper lip,
eyelid) 3
• Asymptomatic, stable lesions with
occasional regression
Special studies
Inverted follicular keratosis
• In situ hybridization and
immunohistochemistry to detect HPV
Histological differential
1. Seborrheic keratosis (especially the 2. Squamous cell carcinoma
irritated variant) • SCC is not well demarcated
• Seborrheic keratosis are raised • Cellular atypia and abnormal
above the surrounding skin mitoses
• Absence of endophytic component • Absence of squamous eddies

Clinical variants • IFK are essentially warts developing within a hair follicle
• None
14
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Solar lentigo
Introduction
Benign pigmented lesion with an increased number of pigmented
keratinocytes.
Histological features Epidemiology

1. Elongation of the rete ridges
• Solar lentigo occurs on sun-exposed skin
2. Basal hyperpigmentation, sometimes quite heavy
in more than 90% of the white population
3. Solar elastosis is almost always present
older than age 60 years, but may be
observed in much younger individuals
as well
1
Pathophysiology
• It has been suggested that solar lentigo
3
is induced by the mutagenic effect of
repeated ultraviolet light exposure
2 • Carriers of one or two of the
melanocortin-1-receptor (MC1R) gene
variants have a 1.5- to 2-fold increased
Solar lentigo risk for the development of numerous
solar lentigines
Histological differential Clinical features

1. Lentigo maligna: • Dark brown to black macules, 3–12 mm
• Presence of irregular nests of melanocytes or more in diameter; often multiple
• Single melanocytes in the upper layers of the epidermis • They are distinguished from common
freckles by their persistence despite
absence of sun exposure
Special studies
• Immunohistochemical analysis: S-100,
HMB-45, Melan-A, and tyrosine
kinase are negative in the pigmented
keratinocytes, but highlight the presence
of melanocytes
Lentigo maligna

• Solar lentigos can be very large and simulate melanoma clinically Clinical Variants
• Solar lentigo may show transition to reticulated seborrheic keratosis
• Hypermelanotic or “ink spot” solar
lentigo
15
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Seborrheic keratosis
Introduction
Seborrheic keratoses are the most common benign skin tumor in older
individuals characterized by well-demarcated papules with a verrucous surface.
They appear “stuck-on” and increase in numbers with age. They are commonly
Epidemiology found on the face, neck, and trunk (especially the upper back), as well as the
• Common in elderly extremities.
• Increase in number with age
• Sunlight seems to play a role Histological features
1. Proliferation of basaloid cells with areas of acanthosis and papillomatosis
Pathophysiology 2. Pseudo-horn cysts
• Monoclonal in origin, indicating clonal 3. Sharp demarcation of the base of the neoplasm
expansion of somatically activating 4. Basket weave hyperkeratosis
mutations in a specific transmembrane • Histological variants include acanthotic, hyperkeratotic, clonal (Borst-
tyrosine kinase receptor, fibroblast Jadassohn appearance), reticulated, irritated and melanoacanthoma variant
growth factor receptor-3
Clinical features 2
4
• Sharply defined, tan to black, flat, 1

papular or nodular lesions with a velvety
3 2
to verrucous surface
• “Stuck-on”, waxy appearance
• Usually asymptomatic with minimal
pruritis
• Frequently located on sun-exposed areas; Seborrheic keratosis Pigmented seborrheic keratosis
trunk, face, upper extremities
Special studies Histological differential

• None 1. Epidermal nevus:
• Clinical history is helpful
• Usually lack pseudocysts
2. Squamous cell carcinoma:
• Atypical keratinocytes involving the entire epidermis, dyskeratosis and
abundant mitoses
Epidermal nevus Squamous cell carcinoma
Clinical variants Important Things To Know

• Dermatosis papulosa nigra • Leser-Trélat sign is the sudden onset of numerous seborrheic keratoses
• Stucco keratosis and may indicate an underlying visceral neoplasm
• Nevoid hyperkeratosis of the nipple
• Oral melanoacanthoma
16
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Warty dyskeratoma Epidemiology
• Warty dyskeratoma occurs mostly in
Introduction middle-aged to elderly adults
Warty dyskeratoma is a benign papulonodular lesion characterized by an
endophytic proliferation of squamous epithelium, typically occurring in relation Pathophysiology
to a folliculosebaceous unit and showing prominent areas of acantholysis. • There are no known etiological factors
Histological features Clinical features

1. Well-demarcated endophytic lesion characterized by prominent acantholytic • Most lesions are solitary flesh-colored to
dyskeratosis brown papules, nodules or cysts with an
2. Suprabasal clefting with formation of villi umbilicated or pore-like center or central
3. Abundant keratin forming a plug within the center of the proliferation keratin plug
4. Corps rounds and grains, which are dyskeratotic keratinocytes present in • Most are 1–10 mm in size. Occasionally
the stratum spinosum and granulosum the lesions are multiple
• Most cases asymptomatic but can be
pruritic and bleed
3 • Foul-smelling cheesy discharge possible
4 • The head and neck region is most
1 commonly involved
2 4 • Does not spontaneously regress
Warty dyskeratoma
Special studies
• Excisional biopsy and immunofluorescent
staining to rule out pemphigus vegetans
1. Benign familial pemphigus (Hailey–Hailey disease)
• Has more acantholysis
• Acantholysis involving large areas of the epidermis
2. Darier’s disease
• Needs clinicopathological correlation
3. Pemphigus vegetans
• Large areas of acantholysis
• Collections of eosinophils in the epidermis
Familial benign pemphigus Darier’s disease Pemphigus vegetans

(Hailey–Hailey)

• The diagnosis is rarely made clinically
• Malignant degeneration has not been associated with warty
dyskeratoma
• HPV is not associated despite the warty dyskeratoma
Clinical variants
• None
17
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Malignant Tumors • Basal cell carcinoma and variants
Basal cell carcinoma and variants
Introduction
Basal cell carcinoma (BCC) is the most common malignant neoplasm in humans.
It is destructive locally and has a tendency to recur, but rarely metastasizes. BCC
varies in aggressiveness and can be associated with multiple syndromes.
• 75% of all diagnosed skin cancers in the
United States are BCCs 1. Irregular collections of basaloid cells
• Predisposing factors include a history of 2. Neoplastic keratinocytes with large oval basophilic nuclei and scant cytoplasm
nonmelanoma skin cancer, Fitzpatrick 3. Clefts between the neoplastic cells and stroma (an artifact produced by the
skin type I and II, prolonged sun exposure loss of mucin during processing)
in youth, immunosuppression, exposure Other features:
to arsenic, fiberglass dust, or dry cleaning • Necrotic tumor cells are present among the basaloid cells and sometimes form
agents, and previous trauma (smallpox central pseudocystic spaces filled with mucinous debris
vaccination site, burn scars)
• BCC can be associated with xeroderma
pigmentosum (XP), Gorlin’s syndrome 1
1
(basal cell nevus syndrome, BCNS), 1
Bazex syndrome (X-linked dominant 2
condition with features of follicular
3
atrophoderma, multiple BCCs, local
anhidrosis, and congenital hypotrichosis)
or Rombo syndrome (an autosomal
dominant condition distinguished by Nodular basal cell carcinoma Basal cell carcinoma
BCC, atrophoderma vermiculatum,
trichoepitheliomas, hypotrichosis, milia,
and peripheral vasodilation with cyanosis) Histological differential
1. Squamous cell carcinoma:
Pathophysiology • Larger and more eosinophilic cells
• BCCs develop from keratinocytes in the basal • No cleft artifact
layer (stem cells) of hair follicles, sebaceous • No peripheral palisading
glands, and interfollicular basal cells 2. Poroma:
• A relationship to embryonic closure lines • Uniform cellular proliferation of basaloid
may exist cells
• The tumor suppressor genes p53 or • Lack necrotic cells
PTCH1 are most commonly mutated • No clefting
• XP and Gorlin’s syndrome have evidence • Lack of stromal changes seen in BCC Squamous cell carcinoma
of PTCH1 mutations
Poroma Trichoepithelioma
Clinical variants
• Nodular
• Superficial (multifocal)
• Morpheaform (infiltrative)
• Fibroepithelioma of Pinkus
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Clinical features
• Pearly red macule, papule, nodule or
plaque most common in sun-exposed
area especially the nose, face and ears
BCC variants • Telangiectasia over the neoplasm
Special studies
• H&E is the stain of choice
• BerEp-4 and cytokeratin 20 to
differentiate Merkel cell carcinoma
superficial basal cell carcinoma Morpheaform or infiltrative

basal cell carcinoma
Morpheaform or infiltrative
basal cell carcinoma
Fibroepithelioma of Pinkus
Fibroepithelioma of Pinkus

• Lichen planus like keratosis can mimic BCC clinically
19
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Malignant Tumors • Squamous cell carcinoma and variants
Bowen’s disease
Introduction
Bowen’s disease is a clinical expression of squamous cell carcinoma in situ of the
skin.

• It occurs predominantly on sun-exposed 1. Full-thickness involvement of epidermis and sometimes the pilosebaceous
skin of older white men, but both sexes epithelium by atypical keratinocytes, dyskeratotic cells, and mitoses
are affected 2. Loss of the granular layer, parakeratosis, and hyperkeratosis
• Invasive carcinoma can develop in up to • Several histological variants have been described: psoriasiform, atrophic,
8% of untreated cases verrucous hyperkeratotic, pigmented and pagetoid variant
Pathophysiology
2
• The exact underlying cause remains 1
unclear; however, it is known that
chronic sun damage disrupts normal
keratinocytic maturation and causes
mutation of the tumor suppressor gene
mutation (TP53)
Clinical features Bowen Disease

• The disease presents as an asymptomatic
well-defined erythematous scaly plaque
Special studies 1. Bowenoid papulosis:
• Immunohistochemical analysis: CK5/6+, • Multiple papules on the anogenital areas of young patients
HMB-45–, CEA– 2. Extramammary Paget’s disease:
• (CK7+, CEA+)
• Sometimes difficult to distinguish from Pagetoid variant
3. Melanoma in situ
• (S-100+, HMB-45+)
• Sometimes difficult to distinguish from Pagetoid variant
Bowenoid papulosis
Extramammary Paget’s disease Melanoma in situ

Clinical variants • Bowenoid papulosis is indistinguishable from Bowen’s disease
• Verrucous histologically
• Ulcerated
• Pigmented
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Keratoacanthoma
Introduction
Keratoacanthomas are rapidly growing variant of squamous cell carcinomas
that may resolve spontaneously leaving an atrophic scar.

1. Invaginating epidermis with a keratin-filled crater. Adjacent epithelium • Keratoacanthomas develop in the older
develops “lips” and shows orthokeratosis, acanthosis, hypergranulosis and age groups, particularly in the sixth and
parakeratosis seventh decades, and there is a male
2. Strands of eosinophilic epidermis invade the dermis. Mitoses are present preponderance
3. Intraepidermal neutrophilic, eosinophilic microabscesses and horn pearls
4. Involuting lesions begin to take on a flattened, less crateriform appearance. Pathophysiology
The inflammatory infiltrate becomes largely lichenoid • Exposure to excessive sunlight is the
most frequently incriminated factor
• DNA sequences of HPV of both genital
and cutaneous types have been detected
1 in up to 55% of keratoacanthomas in
3 2 immunosuppressed patients
Clinical features
4
• Solitary pink or flesh-colored dome-
shaped nodule with a central keratin
Keratoacanthoma Keratoacanthoma plug on the sun-exposed skin. Multiple
keratoacanthoma can occur
• It grows rapidly to a size of 1–2 cm,
Histological differential followed by a stationary period. It has
a tendency to involute spontaneously,
1. Squamous cell carcinoma: this takes 8–50 weeks. Giant
• Intraepidermal microabscesses and tissue eosinophilia are more commonly keratoacanthoma is greater than 2 cm
found in keratoacanthoma and has a predilection for the nose and
2. Warts: dorsum of the hand
• Do not show the degree of atypia seen in keratoacanthomas • Abortive keratoacanthoma is a variant in
• Tend to be exophytic which involution commences at an early
stage
• Keratoacanthoma centrifugum
marginatum is a rare variant
characterized by progressive peripheral
growth with coincident central healing
• Subungual keratoacanthomas grow
rapidly; they are more destructive than
squamous cell carcinoma in this site
Special studies
Squamous cell carcinoma
• None
Clinical variants
• Subungual keratoacanthoma is an
• Keratoacanthomas of the face and neck can metastasize aggressive carcinoma
• Eruptive keratoacanthomas, which can
appear suddenly and in crops
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Squamous cell carcinoma
Introduction
Cutaneous squamous cell carcinoma (SCC) is the second most common cancer
of the skin and accounts for 20% of cutaneous malignancies. Most squamous cell
carcinomas are readily treated with few sequelae. Larger or more invasive lesions
may require aggressive management and have the potential to metastasize.
Epidemiology
• SCC occurs in men about two to three Histological features
times more frequently than it does in Histology will vary based on the different subtypes of SCC, however common
women features are:
• Predisposing factors include: Fitzpatrick 1. Acanthosis
skin types I and II, being middle-aged or 2. Full-thickness intraepidermal proliferation of atypical keratinocytes, cellular
elderly, multiple atypical keratinocytes atypia and mitoses
(AK), a history of nonmelanoma skin 3. Atypical keratinocytes in the dermis (the main feature that distinguishes
cancer, frequent UV light exposure invasive SCC from SCC in situ)
• SCC is associated with 4. Keratinization results in the production of keratin pearls
immunosuppressive therapy Other features:
• SCC is also associated with chronic • Hyperkeratosis and parakeratosis
skin ulcers, prior X ray treatment, • Atypical keratinocytes may be found in the basal layer and often extend
HPV infection, arsenic ingestion, HIV deeply down hair follicles
infection, smoking, genetic syndromes • Histological variants include: acantholytic, adenoid, spindle cell, clear cell type,
such as xeroderma pigmentosum, and signet-ring cell type, verrucous carcinoma, sarcomatoid and pigmented type
toxic exposure to tars and oils
Pathophysiology
• The primary cause of most SCC is
cumulative lifetime UV light exposure;
including PUVA
4
• Inactivation of the tumor suppressor
gene TP53 occurs in up to 90% of all 1
cutaneous SCC lesions. Other tumor
suppressor genes found to be mutated
include P16 and P14 3
2
• Iatrogenic immunosuppression
and DNA repair failure, such as in Squamous cell carcinoma
xeroderma pigmentosum, have also been Squamous cell carcinoma
associated with increased incidence of
SCC
Clinical variants
• Verrucous
• Keratoacanthoma
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Clinical features
• Hyperkeratotic or ulcerated plaque with a
red, inflamed base, a growing tumor, or a
non-healing ulcer, often on sun-exposed
areas such as the head and neck
• SCC can also occur on the lips, inside
the mouth, on the genitalia. It can be de
Histological differential novo or arise from an AK
• SCC is capable of locally infiltrative
1. Hypertrophic AK:
growth, spread to regional lymph nodes,
• Prominent orthokeratosis with alternating parakeratosis
and distant metastasis, most often to the
• Epidermis usually shows irregular psoriasiform hyperplasia and mild
lung. It is usually asymptomatic unless
papillomatosis
perineural invasion is present
• Atypical keratinocytes are confined to the basal layer
• Presence of vertical collagen bundles and some dilated vessels in the
papillary dermis
Special studies
2. Keratoacanthomatous variant of SCC: • Immunoperoxidase staining for
• Exoendophytic lesions with an invaginating mass of keratinizing, well- cytokeratin positivity
differentiated squamous epithelium at the sides and bottom of the lesion
• There is a central keratin-filled crater
• Epithelial atypia and mitoses are not a usual features
• There is a mixed infiltrate of inflammatory cells in the adjacent dermis.
Eosinophils and neutrophils may be prominent, and these may extend into
the epithelial nests to form small microabscesses
Hypertrophic atypical Keratoacanthoma

keratinocytes

• If the tumor is poorly differentiated it is associated with a higher risk of
metastasis
• Patients who develop one SCC have a 40% risk of developing another
SCC within the next 2 years and should be evaluated with a complete
skin examination every 6–12 months
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MELANOCYTIC NEOPLASMS
Benign Neoplasms • Lentigo simplex (juvenile lentigo)
Introduction
Lentigo simplex, is a benign hyperpigmented macule that usually develops at
birth or during early childhood that is due to increased melanin production from
melanocytes. They are not associated with sun exposure or systemic disease.
Histological features
1. Elongation of the rete ridges and increase in number of melanocytes in the
basal layer
Epidemiology 2. Increased amount of melanin in melanocytes, basal keratinocytes and in the
melanophages of the upper dermis
• The frequency has not been determined
• The most common type of lentigo
• Affects all races and genders
1
Pathophysiology 2
• The etiology is unknown

• Lesions are brown to black freckle-like 2
macules caused by increased melanin
production from an increased number of Lentigo simplex Lentigo simplex (high power)
melanocytes in the basal layer
Clinical features Histological differential

1. Solar lentigo:
• The lesions are well circumscribed, oval
• More significant elongation of the rete ridges, composed of single layers of
to round, light brown to black macules
deeply pigmented basaloid cells and melanocytes
with regular borders
2. Junctional melanocytic nevus:
• They measure only a few millimeters in
• Well-circumscribed nevus cell nests either entirely within, or in contact with
diameter (usually <5 mm)
the lower epidermis
• Lentigo simplex can occur anywhere on
the body
• The borders are irregular and ill-defined
Special studies
• Mart-1, Mel-5, and DOPA histochemis-
try tests can be done to show increased
number of melanocytes without nest
formation in the basal epidermal layer
Solar lentigo Junctional nevus

• Multiple lentigines may or may not be associated with numerous autosomal
dominant syndromes: LEOPARD syndrome (Lentigines, Electrocardiographic
conduction defects, Ocular hypertelorism, Pulmonary stenosis, Abnormali-
ties of genitalis, Retardation of growth and Deafness), Carney complex or
NAME/LAMB syndrome (Nevi, Atrial myxoma, Myxoid neurofibroma,
Ephelides/Lentigines, Atrial myxoma, Mucocutaneous myxoma, Blue nevi),
Peutz-Jeghers syndrome (mucocutaneous lentigines which are present at
Clinical variants birth or appear during childhood in combination with intestinal polyposis)
• None
24
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Melanocytic nevi
Introduction
Melanocytic nevi are common pigmented lesions and can be junctional,
compound or intradermal.

1. Junctional nevus: equidistant nests and single melanocytes at the dermal- • The prevalence of nevi in the general
epidermal junction, regular hyperplasia of the rete ridges. The nevus cells population is not well documented
with regular, round to cuboidal, or rarely spindle-shaped appearance • Both sexes are approximately equally af-
2. Compound nevus: presence of an epidermal and dermal component of nevus, fected
arranged in orderly nests or cords, a gradual decline in the number of nests • White people have a greater prevalence of
from the epidermis down to the superficial and reticular dermis, individual nevi than darker-skinned people, and on
nevus cells, dispersed among collagen fiber bundles in the reticular dermis average have approximately 20 acquired
3. Intradermal nevus: presence of nevus cells only in the dermis nevomelanocytic nevi
• Acquired melanocytic nevi typically de-
2 velop before the third decade of life, and
2
begin to disappear thereafter
• Genetic factors play a role in the number
of acquired melanocytic nevi
Pathophysiology
1
• Melanocytic nevi are thought to originate
Junctional nevus Compound nevus from cells, termed melanoblasts, which mi-
grate from the neural crest to the epidermis
Histological Clinical features

3
differential • A round or oval, well-circumscribed,
Junctional nevus: uniformly colored macular lesion with
1. Lentigo simplex: smooth, regular borders
• Variable basal hyperpigmentation • Color varies from brown to black and
• Increased number of single melanocytes their size is always less than 1 cm in
in the basal layer diameter
Intradermal nevus • No nest formation • It may develop anywhere on the body
2. Melanoma in situ: surface
• Irregular proliferation of nests and single melanocytes in the epidermis • Compound and intradermal nevi can pres-
• Single melanocytes can be present in the upper levels of the epidermis ent as elevated to dome-shaped or polyp-
Compound nevus/intradermal nevus: oid configurations
1. Malignant melanoma: • Older nevi, predominantly on the trunk,
• Cytological atypia and numerous mitoses in the dermis may become pedunculated with time
Special studies
• Hematoxylin and eosin
is the stain of choice
• S-100, HMB-45, and
Melan-A stain melano-
cytic lesions
Solar lentigo Melanoma in situ Malignant melanoma
Important Things To Know Clinical variants

• Sun exposure promotes the development of melanocytic nevi • Unna’s • Spitz nevus
• Miescher • Reed’s nevus
• Clark’s • Blue nevus
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Halo nevus (Sutton’s nevus)
Introduction
Halo nevi are melanocytic nevi surrounded by a zone of depigmentation or halo
of leukoderma. The onset of the ring of depigmentation occurs over several
weeks to months. These lesions are more common in children and young adults.
Epidemiology In most cases, the central nevus undergoes involution, with subsequent re-pig-
• Overall incidence of halo nevi in individ- mentation of the area of depigmentation.
uals under age 20 is probably <1%
• The majority of halo nevi occur in first 5 Histological features
decades after birth, with a mean age of 1. The central nevus may be compound, junctional or dermal
approximately 15 years 2. A dense band-like inflammatory infiltrate of the papillary dermis, in early
• Approximately 20% of individuals with stages, in which lymphocytes and histiocytes predominate
halo nevi have vitiligo
• Halo nevi are equally common in all Other features:
races and both sexes • At later stages, few, if any, distinct nevus cells can be identified
• Decrease or total absence of melanocytes and increase in Langerhans cells in
Pathophysiology depigmented zone
• Pathophysiology is not completely under-
stood, although both cellular and humor- 1
al immunological factors are implicated 2
• Depigmentation of the central nevus is
believed to result from the immunologi-
cally mediated destruction of nevus cells
by CD8+ T cells
• Depigmentation of the halo area may
result from the destruction of melano-
cytes secondary to the diffusion of an
Histopathology of halo nevus Halo nevus high power
unknown cytotoxic factor
highlighted prominent
Clinical features melanocytes and lymphocytes
• The central nevus typically is 3–6 mm in Histological differential

diameter, has homogeneous coloration,
and is well circumscribed 1. Melanoma:
• The depigmented halo measures in width • Patchy inflammatory infiltrate, more prominent on the periphery
from a few millimeters to several centi- • Increased cellularity
meters and is usually symmetric • Mitosis may be found
• Predominantly located on the back, but • No maturation with progressive descend
may be found in any location
• 25–50% of affected individuals have mul-
tiple halo nevi
Special studies
• Melan-A/MART-1 stain can be used to
identify any residual melanocytes
Malignant melanoma

• Halo nevi are believed to be an immunologic reaction to a nevus
• The presence of one or more halo nevi may indicate incipient vitiligo
• Early lesion of halo nevi can mimic melanoma and biopsy may be re-
Clinical variants quired for the proper diagnosis
• None
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Spitz nevus
Introduction
A Spitz nevus is a type of melanocytic nevus which is usually found in chil-
dren and young adults.

1. Nests of large epithelioid cells and/or spindle cells extending in a wedge • The prevalence of Spitz nevi in the general
configuration from the epidermis to the reticular dermis population of Australia is 1.4 per 100,000
2. Maturation with progressive descend, with larger cells near the epidermis • The majority of Spitz nevi are acquired
and smaller cells at the base after birth, but up to 7% are estimated to be
3. The large epithelioid and spindle cells have an abundant amphophilic congenital in origin
cytoplasm, open chromatin, little, if any, melanin pigment, and prominent • Spitz nevi occur in all age groups, with one-
eosinophilic or amphophilic nucleoli third of cases in individuals less than 10
4. Epidermal hyperplasia with acanthosis, papillomatosis and hyperkeratosis years, one-third between 10 and 20 years,
5. Clefts between the epidermal and the melanocytic component and one-third over 20 years of age
6. Kamino bodies that contain basement membrane material are usually found • However, they are rare in individuals over
at dermoepidermal junction the age of 40 and are predominantly found
• Pigmented spindle cell of Reed is characterized by prominent melanin pig- in light-skinned individuals
ment in addition to other features • Both sexes are approximately equally af-
• Intraepidermal Spitz nevus is characterized by a proliferation of epithelioid fected
melanocytes in the epidermis without a dermal component
• Intradermal Spitz nevus is characterized by the presence of epithelioid me- Pathophysiology
lanocytes in the dermis without an epidermal component • The pathophysiology of Spitz nevi is greatly
unknown, and the majority of them have
4
no known precipitated cause
• The widespread onset of Spitz nevi have
been linked with HIV infection, chemother-
1 3 apy, Addison’s disease, pregnancy, puberty,
6
and trauma
2
5 • The association with pregnancy and puber-
ty indicates a possible hormonal causation
Spitz nevus
Spitz nevus
Clinical features
• A dome-shaped, well-circumscribed, hair-
Histological differential less papule or nodule often accompanied by
telangiectasia
1. Melanoma: • The color varies from pink to tan and their
• The lesions are asymmetric size is ranges in diameter from 2 mm to
• Poorly circumscribed 2 cm. In 95% of patients, the nevus is less
• No maturation with progressive de- than 1 cm in diameter
scend • They are predominantly found on the head
• Mitotic figures in the deeper areas of and neck area, although they may be found
the lesion on any part of the body
• Single melanocytes at all levels of the • Multiple Spitz nevi may arise in a dissemi-
epidermis nated or agminated pattern
Spitzoid melanoma
• No epidermal hyperplasia
Special studies
Important Things To Know • Hematoxylin and eosin is the stain of
choice
• It is advised that small Spitz nevi be completely excised as a precaution
• S-100, HMB-45, and Melan-A stain melano-
since differentiation from melanoma is often difficult
cytic lesions
• Recurrences rates after the incomplete excision of a Spitz nevus range
from 7–16%
• Although benign, melanocyte nests from a Spitz nevus may disseminate
to lymph nodes Clinical Variants
• Agminated
27
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Spitz nevus variants
Pigmented spindle cell of Reed Pigmented spindle cell of Reed
Intraepidermal Spitz nevus Intraepidermal Spitz nevus
Intradermal Spitz nevus
Intradermal Spitz nevus
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Blue nevus
Introduction
Blue nevus (BN) is a benign, usually intradermal, melanocytic lesion charac-
terized by pigmented dendritic spindle-shaped melanocytes and more rarely,
epithelioid melanocytes. The melanocytes are usually separated by thickened
collagen bundles. Epidemiology
Histological features • BN is relatively frequent, has predilection
for females
1. Pigmented spindle-shaped melanocytes • Presents mainly in young adults between
2. Thickened collagen bundles in mid and upper dermis the second and fourth decades
• Although most tumors are acquired, con-
Epithelioid blue nevus: genital examples have been documented
• Dermal aggregates of round to oval melanocytes • Familial cases may be seen and usually
• Centrally placed nuclei (fried egg appearance) present with multiple lesions
• Coarse granules of melanin in their cytoplasm
Deep penetrating nevus: Pathophysiology
• Vertically oriented neoplasm • Blue nevi represent benign tumors of
• Epithelioid and spindle melanocytes in the dermis dermal melanocytes
• Epithelioid melanocytes can have spitzoid features • In general, melanocytes disappear from
• Melanocytes can be present around adnexal structures the dermis during the second half of
Combined blue nevus: gestation, but some residual melanin-pro-
• Blue nevus with overlying junctional, compound or intradermal nevus ducing cells remain in the scalp, sacral
region, and dorsal aspect of the distal
1 extremities
2 • Somatic activating mutations in GNA11
and GNAQ (primarily the latter) have
been detected in 65–75% of blue nevi
Clinical features
• The most common presentation con-
sists of a single asymptomatic, relatively
well-circumscribed, dome-shaped blue
Blue nevus or blue-black papule less than 1 cm in
Histological differential diameter
• The characteristic blue color is produced
1. Desmoplastic melanoma: by the Tyndall effect
• Proliferation of spindle cells with variable degree of atypia in the dermis • Tumors may rarely present as a plaque
• Patchy infiltrates of lymphocytes • Eruptive lesions have rarely been docu-
• In some cases there is an epidermal component mented
2. Tumoral melanosis: • The anatomical distribution is wide, but
• These are lesion in which there are only melanophages in the dermis most lesions occur on the distal upper
• The melanophages are loaded with coarse granules of melanin limbs (particularly the dorsum of the
hand), followed by the lower limbs, scalp,
face and buttocks
Tumoral melanosis
Clinical variants
Desmolastic melanoma • Speckled BN
• Hypopigmented BN
• Widespread BN
29
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Special studies Blue nevus variants
• Diffusely positive for melanocytic mark-
ers including S-100, HMB-45, Melan-A
and microphthalmia transcription factor
(MITF-1)
Epithelioid blue nevus
Deep penetrating nevus
Combined nevus Combined nevus

• Tyndall effect explains the blue clinical appearance due to deep dermal
deposits of melanin which absorbs longer wavelengths of light (red) and
reflects shorter wave lengths (blue)
30
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Malignant Lesions • Malignant melanoma and variants
Introduction
Malignant melanoma (MM) is a skin cancer of the melanocytes, the pigment-
producing cells of the skin. It has the ability to metastasize to any organ in the
body, especially the brain and heart.
• Melanomas in situ (MIS) Epidemiology
1. Proliferation of irregular nests with areas of confluence and single melano-
cytes in epidermis • Risk factors: fair skin, history of sun-
2. Single melanocytes at burns, more than 50 moles, atypical
different levels of the moles, close relative who had melanoma
epidermis including the • Only 4% of all skin cancers are MM, but
2
stratum corneum MM makes up the majority (74%) of skin
1 cancer-related deaths worldwide.How-
ever, low risk melanoma patients (Bres-
Melanoma in situ low’s thickness <1 mm) have a 90% cure
rate when the cancer is found early and
Invasive melanoma appropriately excised
Other features: • It is the sixth most common cancer in the
• In some cases, melanocytes replace com- United States
pletely the basal layer of the epidermis 1 • Current lifetime risk is 1 per 60 Americans
• Solar elastosis; when melanomas developed 1 for invasive MM in 2008, 1 per 32 Ameri-
in sun-exposed areas (lentigo maligna) cans if noninvasive MM is included
• Highest incidence is in Australia and
• Invasive melanomas New Zealand:
1. Atypical melanocytes in the dermis o Australia and New Zealand incidence
Other features: in 2002: 37.7 per 100,000 men and
• Neoplastic cells can form nodules (nodular melanoma) 29.4 per 100,000 women
o North America incidence in 2002: 6.4
Acral-lentiginous and mucosal melanoma:
per 100,000 men and 11.7 per 100,000
• Presence of dendritic melanocytes
women
• Containing coarse granules of melanin A
• Extension into the upper levels of the epidermis
Desmoplastic or neurotropic melanoma:
• Proliferation of spindle cells within the dermis
• Minimal atypia
• Resemble other spindle cell proliferations including scars
• One characteristic feature is the presence of lymphoid aggregates
• An epidermal component may or may not be present
There are many other types of melanomas:
a. Amelanotic melanomas
b. Nevoid melanomas
c. Melanoma simulating Spitz nevus (spitzoid melanoma)
d. Melanoma with small nevus-like cells (small cell melanoma) Spitz nevus
e. Clear cell sarcoma: melanoma of soft parts
1. Spitz nevus:
• Symmetric lesion
• Spindle and/or epithelioid melanocytes which mature with progressive descend
• Epidermal hyperplasia
• Kamino bodies
• Clefts between the epidermal and melanocytic component
2. Mammary and extramammary Paget’s disease:
• Melanoma in situ needs to be differentiated from
Paget’s disease
• In MIS atypical melanocytes replaced the basal layer,
which is spared in Paget’s disease 31
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Pathophysiology Melanoma variants
• There are both genetic and environmen-
tal factors that play a role in the develop-
ment of MM
• The genetic factors involved in develop-
ment of melanoma are mutations in
chromosome 9p21.25, cyclin-dependent
kinase inhibitor 2A (CDKN2A) and
cyclin-dependent kinase 4 (CDK4). All
are tumor suppressor genes
• The environmental factors correlated Melanoma of back Nodular melanoma
with MM are intense periods of sun
exposure and living at higher elevations
in closer proximity to the sun
Clinical features
• ABCDEs of diagnosing melanoma
(Asymmetry – one side unlike the other;
Border – irregular, scalloped or poorly
defined border; Color – variation in color
within the lesion including shades of tan, Acral melanoma Subungual melanoma
brown, black, white, red or blue; Diam-
eter – often melanoma lesions are 6 mm
in diameter when diagnosed, but can be
smaller or larger; Evolution/Elevation/
Enlargement – any mole or skin lesion
that changes size, shape or color should
be evaluated for melanoma)
• Can occur anywhere on the skin, nails
and mucosae, regardless if sun exposed,
but most commonly occurs on the backs,
arms of men, and legs of women Acral Melanoma
• Can appear on previously normal skin or
moles
Special Melanoma with in transit

studies metastasis
• Primary cutaneous
melanoma is can be
seen in hematoxylin
and eosin sections
• Melanomas are positive
for S-100, Melan-A,
pan-melanoma and
HMB-45 positive
• Desmoplastic melano-
mas are S-100 posi-
tive but negative for
Melan-A and HMB-45 Desmoplastic
melanoma
• Tumor thickness is the best prognostic marker
• The presence of metastases indicates a poor prognosis; the long-term
Clinical Variants survival rate is only 5%
• Acral-lentiginous melanoma (ALM) accounts for 5–10% of primary cuta-
• Melanomas in sun-exposed skin
neous MMs and most common melanoma in Asians (up to 45%) and in
• Melanomas in skin not exposed to sun
blacks (up to 70%). Occur on the soles, palms, fingernail or toenail beds
• Acral melanomas
• Mucosal melanomas
32
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TUMORS OF CUTANEOUS
APPENDAGES
Hair Follicle Tumors • Trichoepithelioma
Introduction
Desmoplastic trichoepithelioma is a histological variant of trichoepitheliomas
with extensive stromal sclerosis (desmoplasia); it occurs almost always on the
face.
Trichoepitheliomas are benign tumors derived from the hair follicle. Some
regard it as a distinct variant of trichoblastoma.
1. Well-circumscribed neoplasm Epidemiology
2. Collections of uniform basaloid cells in reticulate or cribriform pattern
3. Stromal clefts • Appear around puberty
4. No retraction artifact between the neoplastic cells and the stroma
5. Papillary mesenchymal bodies Pathophysiology
6. Horn cysts and calcification • It is regarded as poorly differentiated
7. Fibrous stroma hamartomas of the hair germ
Desmoplastic trichoepithelioma: • Multiple familial trichoepitheliomas have
• Composed of cords and strands of basaloid cells with hyperchromatic nuclei an autosomal dominant mode of inheri-
and small amounts of cytoplasm tance due to a mutation in the CYLD gene
• The neoplastic cells are surrounded by a characteristic rim of collagen
• Prominent fibrotic stroma Clinical features
• Calcification and foreign body granulomas • Three distinct types: solitary, multiple,
• Tadpole- or comma-shaped epithelial projections (paisley-tie pattern) and desmoplastic
o Solitary and multiple have identical
histological features
o Desmoplastic is a distinct entity and
7
will be discussed separately
1 c
5
6
3 2 e Solitary trichoepithelioma:
• Small, skin-colored papules on the face,
4 b especially around the nose, upper lip,
and cheeks. Occasionally develop on the
d
a trunk, neck, scalp, and lower extremities
Trichoepithelioma Multiple trichoepithelioma (epithelioma
Desmoplastic trichoepithelioma adenoids cysticum):
• Numerous, small papules distributed on
the face, usually around the nasolabial
folds, forehead, chin, and preauricular
area; lesions may coalesce to form plaques
and nodules
• Typical onset in childhood or puberty
• Usually inherited in autosomal dominant
fashion but may occur sporadically
• Benign, but there are documented cases of
basal cell carcinoma (BCC) development
in trichoepithelioma
• The Brooke-Spiegler syndrome is the asso-
ciation of multiple trichoepitheliomas with
cylindromas and/or spiradenomas
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Desmoplastic trichoepithelioma:
• More common in women and young
adults 1. Syringoma:
• Types: solitary familial desmoplastic • Composed of cords, strands and collections of cells embedded in a sclerotic
trichoepithelioma, multiple familial, and stroma
non-familial tumors • The cells are larger and have an eosinophilic cytoplasm
• Usually present as asymptomatic, firm, • No horn cysts, foreign body granulomas or calcification
solitary hard annular lesion with raised • Cells contain carcinoembryonic antigen (CEA) but not involucrin
border and depressed center • Usually multiple and periorbital
• Do not grow more than 1 cm in diam- 2. Basal cell carcinoma:
eter; benign with no risk for development • Is asymmetrical
of carcinoma • Irregular collections of basaloid cells
• Horn cysts, calcification, and papillary mesenchymal bodies are rare
Special studies • Clefts between epithelium and stroma
• Immunohistochemical staining: strong
reactions for keratins (CK) 5/6 and CK8
Syringoma
Basal cell carcinoma

Clinical variants • Desmoplastic trichoepithelioma may be difficult to differentiate from
morpheaform BCC or microcystic adnexal carcinoma in small or partial
• Solitary biopsies
• Multiple
• Desmoplastic
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Trichoblastoma
Introduction
Trichoblastoma is a benign tumor with mostly follicular germinative differentia-
tion. It is likely to be on a spectrum with trichoepithelioma (also called imma-
ture, solitary, and giant trichoepithelioma).
Epidemiology
Histological features • Adults
1. Circumscribed dermal tumor with no epidermal connections • Affects males and females equally
2. Peripheral palisading of nuclei
3. Follicular differentiation resembling hair bulbs and papillae Pathophysiology
4. Fibrotic stroma
• It is constituted largely of follicular ger-
5. Clefts in the stroma
minative cells
4 Clinical features
3
1 5 • Slow-growing, solitary, large (>1 cm)
2 nodule in the deep dermis and subcutis
• Any location, especially scalp, face,
trunk, and genital area
• Usually does not involve distal extremi-
ties
Trichoblastoma Trichoblastoma Special studies

• CK7, CK8, and CK19 expressed
1. Trichoepithelioma:
• Smaller and more superficial than trichoblastoma
2. Basal cell carcinoma:
• Cleft between epithelium and stroma
• Myxoid stroma
Trichoepithelioma Basal cell carcinoma

• Associated with nevus sebaceous
Clinical variants
• None
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Trichofolliculoma
Introduction
Trichofolliculomas are rare pilar tumors.
Epidemiology 1. One or several dilated follicles from which many miniaturized hair follicles
• Mostly occurring during adulthood radiate with different degrees of differentiation
• No sex predilection 2. Central follicle opens up on surface, with keratinous material and sometimes
villous hairs
Pathophysiology 3. Follicles branching to secondary or tertiary follicles
• It is a follicularly differentiated hamar- 4. Relative cellular connective tissue stroma
toma
Clinical features 2
1
• Usually presents as a solitary papule or
nodule on the face, scalp, or sometimes 4
the upper trunk; about 0.5 cm in diam-
eter 3
• May be centrally umbilicated, with tuft of
fine hairs emanating from it
• Clinically, may be confused with a BCC Trichofolliculoma
or nevus
Special studies
• None
1. Dilated pore of Winer:
• Instead of small hair follicles, there are finger-like epithelial projections that
radiate into the surrounding dermis
2. Pilar sheath acanthoma:
• Similar to dilated pore of Winer, but with collections of thick acanthotic epi-
thelium
Pilar sheath acanthoma
Dilated pore of Winer

• There is a variant of trichofolliculoma in which large sebaceous follicles
connect to a central cavity or sinus termed sebaceous trichofolliculoma
Clinical variants also known as folliculosebaceous cystic hamartoma
• None
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Pilar sheath acanthoma Epidemiology
• Rare follicular hamartoma occurring in
Introduction middle-aged to elderly individuals
Pilar sheath acanthoma (PSA) is a benign adnexal neoplasm. Clinically, it • No gender predilection
resembles a comedo with a central keratotic plug. Histologically, it has a dilated
infundibulum lined by prominent acanthotic epithelium composed of cells with Pathophysiology
an eosinophilic cytoplasm. • It is a follicular neoplasm differenti-
ated toward the infundibulum and the
Histological features isthmus
1. Central infundibular cystic cavity opening to the epidermal surface and ex-
tending down into lower dermis Clinical features
2. Cyst filled with soft keratinaceous material • Solitary, flesh-colored papule or nodule
3. The cyst wall composed of an acanthotic lobular epithelium forming buds. with small central depression and kera-
Cells with ample eosinophilic cytoplasm and centrally placed nuclei resemble totic plug
the isthmus of the hair follicle • Most commonly occurs on skin of the
upper lip
2
1 4
2
Special studies
• None
2 3
3 Pilar sheath acanthoma
Pilar sheath acanthoma
1. Dilated pore of Winer:
• Larger opening of cystic cavity to epidermal surface
• The cells of the epithelium lining the cystic wall resemble the infundibulum of
the hair follicle. The collections of cells are also less prominent
• Foci of keratinization of lobular buds not seen
2. Trichofolliculoma:
• Radiation of small hair follicles from the wall of the central cyst
• Occasional presence of fine, colorless hair
• Prominent fibrovascular stroma not seen in PSA
Dilated pore of Winer

Trichofolliculoma

• No malignant potential for PSA has been documented and further treat-
ment is unnecessary
• PSA is not associated with a systemic disease Clinical variants
• None
37
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Epidemiology Tumor of the follicular
• Rare condition with relative frequency of
3 to 10 per 100,000
infundibulum
• Most often affects middle-aged or elderly
patients with female predominance
Introduction
Tumor of the follicular infundibulum (TFI) is an uncommon benign adnexal
Pathophysiology neoplasm. It is a nonspecific lesion seen in middle-aged or older individuals,
and often occurs on the face or scalp. The characteristic histopathological fea-
• TFI is thought to originate from the
ture is a subepidermal plate-like proliferation.
infundibulum with differentiation toward
the isthmus cells, although the reason for
the proliferation is unknown
1. Horizontal plate-like proliferation of pale, isthmic keratinocytes in the su-
Clinical features perficial dermis
2. Reticulate structure with multiple connections to the overlying epidermis
• Solitary, flesh-colored or sometimes
3. Sharp demarcation of the lateral edges of the lesion with peripheral palisading
hypopigmented macule, thin papule or
plaque
• Sometimes they may appear slightly 2
atrophic 2
2
• Predilection for face and scalp
• Often diagnosed incidentally upon exci-
sion of other tumors
• TFI may occur in an eruptive fashion
Tumor of the
Special studies follicular
• None infundibulum 3
1
• Composed of basaloid cells with large nuclei and small amounts of cyto-
plasm
• BCC does not form a plate-like proliferation in the dermis
• BER-EP4 is positive
2. Trichilemmoma:
• Characterized by an exophytic nodular proliferation of cells with a pale
cytoplasm
• Squamous eddies present in variable amounts
Trichilemmoma Basal cell carcinoma

Clinical variants • TFI can be clinically confused with basal cell carcinoma
• Solitary
• Multiple or eruptive
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Sebaceous Tumors • Benign neoplasms
Sebaceous hyperplasia
Introduction
Sebaceous hyperplasia is a common, benign and asymptomatic condition of se-
baceous glands in adults of middle-aged or older. There is no known potential
for malignant transformation.
Epidemiology
Histological features • Common in aging adults, reported to
occur in approximately 1% of the healthy
1. Enlarged sebaceous gland with multiple mature sebaceous lobules or acini
population and 25% of the population over
2. Lobules having one or more basal cell layers
age 30
• There is no relationship between the skin
type and the occurrence of these lesions
2
• There is a higher prevalence of sebaceous
1 hyperplasia in transplant patients
• The difference in prevalence between
sexes is unknown
Pathophysiology
• The etiology remains unclear
• A decrease in the circulating levels of
androgen associated with aging is thought
Histological differential to be an underlying cause
• Postulated cofactors include ultraviolet
1. Nevus sebaceous:
radiation and long-term immunosuppres-
• Lobules are aberrant
sion
• Ducts open into the epidermis
• In some cases presence of apocrine glands, trichoblastomas and syringocyst-
Clinical features
adenoma papilliferum • One or more whitish-yellow or skin-col-
2. Sebaceous adenoma: ored papules that are soft and vary in size
• More than two cell layers of germinative epithelium from 2–9 mm
• Often asymptomatic, commonly found on
the central and upper face
• Occasionally they are also located on the
chest, upper arms, areola, oral mucosa,
and vulva
• These papules have a central umbilication
that corresponds to a central follicular
infundibular ostium
• Some papules may have telangiectasias
• Beaded lines represent a unique expres-
Nevus sebaceous sion of sebaceous gland hyperplasia in
which a linear array of hyperplastic seba-
ceous glands is present in the vicinity of
Sebaceous adenoma the clavicle or on the neck
• Biopsy is occasionally indicated to exclude
BCC
Important Things To Know Special studies
• Dermoscopy may be useful in the clinical diagnosis of nodular basal cell • None
carcinoma versus sebaceous hyperplasia
• Dermoscopy shows a haphazard distribution of vessels on the surface
of basal cell carcinoma, whereas the vessels in sebaceous hyperplasia oc-
cur only in the valleys between the small yellow lobules Clinical Variants
• None
39
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Sebaceoma
Introduction
Sebaceomas are distinctive benign neoplasms of adnexal epithelium histologi-
cally differentiating toward sebaceous cells. Clinically, these tumors present as
yellow to orange papules or nodules on the face or scalp of older individuals and
Epidemiology can be associated with the Muir-Torre syndrome.
• Tends to occur in individuals >40 years
of age Histological features
• Both genders seem to be affected equal- 1. Symmetric, well-circumscribed lesions composed of lobules with smooth bor-
ly with a slight predilection for women ders localized in the dermis which may extend into the subcutaneous fat
2. Individual lobules show an admixture of basaloid cells or seboblasts and small
Pathophysiology clusters of mature sebaceous cells
• It is a neoplasm composed of immature 3. Seboblasts predominate in sebaceoma and mature sebaceous cells may be
sebaceous cells admixed with scattered present only focally
mature sebocytes
• Some lesions are associated with Muir- 1
2 2
Torre syndrome
Clinical features 3
• Solitary yellow or orange, smooth-

surfaced papule or nodule with rolled
borders
• Anatomic site: face, scalp, and neck
• Slowly growing, usually asymptomatic Sebaceoma Sebaceoma
and <1 cm in diameter
• Ulceration and bleeding may occur Histological differential
• Association with Muir-Torre syndrome
(characterized also by multiple kerato- 1. Sebaceous adenoma:
acanthomas and visceral carcinomas, • More superficial than sebaceoma
especially colonic adenocarcinoma) • Seboblasts are localized at the periphery
while mature sebocytes are present in the
Special studies central part of the neoplasm and are the
predominant cell
• No histologic features of sebaceoma • Mitotic figures can be found in seboblasts
could reliably pinpoint the association but are not conspicuous
of Muir-Torre syndrome, but loss of Sebaceous adenoma
2. Sebaceous carcinoma:
nuclear staining for MLH-1 or MSH-2 • Usually large, asymmetric, poorly cir-
suggests microsatellite instability cumscribed
• Abundant necrosis (necrosis en masse)
• Nuclear atypia often striking
• Numerous and sometimes abnormal
mitotic figures
Sebaceous carcinoma

• There are scattered mitoses, but the tumor lacks prominent atypia
• Histopathologists should alert clinicians to the utility of having a patient
with sebaceoma investigated for other cutaneous signs and internal
evidence of Muir-Torre syndrome
• Muir-Torre syndrome is an inherited autosomal dominant germline
mutation in one of the DNA mismatch repair (MMR) genes, most com-
Clinical variants monly hMSH
• None
40
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Sebaceous adenoma
Introduction
Sebaceous adenoma (SA) is a benign cutaneous neoplasm of the adnexa with
sebaceous differentiation. A spectrum of morphologic features and varying
degrees of differentiation can occur within one neoplasm.
Epidemiology
Histological features • The exact incidence is unknown with no
1. Multiple well-defined enlarged sebaceous lobules particular geographical location showing
2. Frequent attachment to epidermis with epidermal thinning higher incidence rates
3. Small, undifferentiated, germinative basaloid cells at the periphery • No reported predisposition for any par-
4. Transitional cells and mature sebocytes in the center of the neoplasm ticular race
5. Varying ratio of basaloid and transitional cells to sebocytes, traditionally • Men and women are equally affected
more than 50% are sebocytes • Most common on the face or scalp of
6. Lobules may contain duct-like structures middle-aged and older individuals (i.e. 50
years or greater)
• The mean age of onset is 60 years
1 2 5
1
3
4 Pathophysiology
• All sebaceous glands in the body have
the potential to develop into sebaceous
neoplasms. SAs are cutaneous adnexal
Sebaceous adenoma
tumors that show varying degrees of
sebaceous differentiation
Clinical features
Histological differential • Often a solitary yellow nodule found on
the head, neck, and especially face of
1. Sebaceous hyperplasia: patients 50 years or older
• Has only one or two cell layers of germinative epithelium • Gradual onset of small (<0.5 cm up to
• Relatively normal and uniform sebaceous lobules 5 cm plus), smooth, yellow papule/nod-
2. Sebaceoma: ule, with possible polypoid appearance or
• More than 50% of cells are small germinative basaloid cells central umbilication
• Occasionally, tumors may be seen at
other sites, including the trunk and the
legs
• Can be associated with Muir-Torre
syndrome (characterized also by multiple
sebaceous keratoacanthomas and visceral
carcinomas, especially colonic adenocar-
cinoma)
Special studies
Sebaceoma • No histologic features of SA could reli-
ably pinpoint the association of Muir-
Torre syndrome, but loss of nuclear
staining for MLH-1 or MSH-2 suggests
microsatellite instability and the syn-
drome

• Histopathologists should alert clinicians to the utility of having a patient
with sebaceous adenoma outside the face investigated for other cutane-
ous signs and internal evidence of Muir-Torre syndrome Clinical variants
• None
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Sebaceous Tumors • Malignant tumors
Sebaceous carcinoma
Introduction
Sebaceous carcinoma is an aggressive, rare adnexal tumor characterized its ten-
dency for local recurrence and metastasis. They usually manifest as a nodule but
may have other clinical presentations, which may result in a delayed diagnosis.
Epidemiology 1. Irregular lobules or sheets of cells sepa-
rated by a fibrovascular stroma
• Unknown etiology 2. Variable sebaceous differentiation in the 1
• Risk factors form of cells with vacuolated bubbly cyto-
o Older age plasm and scalloped nuclei 1
o Female 3. Necrosis which may be massive (necrosis
o Higher incidence in Caucasian, Asian, en masse)
and Indians 4. Neoplastic cells show marked nuclear
o Irradiation pleomorphism and numerous mitotic fig- 3
o Pre-existing sebaceous lesions ures, many of the atypical are identified
o Muir-Torre syndrome 5. Smaller basaloid cells and squamous dif-
o Immunosuppression ferentiation may be present
Pathophysiology Other features:

• Pagetoid spread to the epidermis is seen
5 2
• May originated from cells within seba- in numerous cases

4 4
ceous glands
Sebaceous carcinoma
Clinical features
• Most commonly presents as a painless, Histological differential
erythematous nodule or plaque that may 1. Basal cell carcinoma:
be ulcerated or crusted, occasionally may • Smaller cells with more basophilic nuclei
display a yellowish coloration and smaller cytoplasm which is not vacu-
• Early ocular lesions are very commonly olated
misdiagnosed as blepharitis, chalazion or • Less atypia
ocular rosacea • Cells are more uniform
• About 75% occur in the periocular region 2. Sebaceoma:
but also occur elsewhere including head • Circumscribed
and neck and less commonly on the • Symmetrical
trunk • Higher percentage of differentiated to
undifferentiated cells Basal cell carcinoma
Special studies • Less nuclear atypia and mitosis
• EMA (epithelial membrane antigen) and
adipophilin immunoperoxidase staining
can be used to confirm sebaceous dif-
ferentiation
• May be associated with the Muir-
Torre syndrome
• Due to the pagetoid pattern, seba-
ceous carcinoma can be confused
with pagetoid Bowen’s disease and
melanoma Sebaceoma
• Sometimes the cells extend deeply
and can involve the subcutaneous
tissue and even the underlying
Clinical variants muscle
• None
42
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Sweat Gland Neoplasms • Benign neoplasms
Apocrine adenoma Epidemiology
• Rare
Introduction
Apocrine adenoma is a benign neoplasm which clinically presents as a smooth Pathophysiology
nonspecific nodules or papules and histologically as apocrine epithelium in • Benign neoplasm arising from apocrine
either tubular or papillary patterns. glands
• Unknown etiology
1. Circumscribed dermal tumor composed of lobules or tubules lined by apo- Clinical features
crine epithelium • Typically smooth nodule or papule
2. The neoplastic cells show an eosinophilic cytoplasm and areas of decapita- • Found on cheek, axillae, breast, genital,
tion and secretion and perianal region or in association with
3. Papillary projections without stroma into tubule’s lumina an organoid nevus
• Biopsy required for diagnosis
Special studies
• Immunoperoxidase staining for myo-
1 epithelial cells (S-100 and actin) helps to
3 distinguish from adenocarcinoma
2
Apocrine adenoma Apocrine adenoma
1. Hidradenoma papilliferum:
• Well-defined dermal nodular configuration
• An almost exclusive localization to the vulvar and perineal areas
• A predominance in women
2. Syringocystadenoma papilliferum:
• Prominent cystic invagination lined by squamoid and apocrine epithelium
• Prominent plasmacellular infiltrates in the stroma
• Localization to the head and neck area
• Frequent association with nevus sebaceus
Hidradenoma papilliferum
Syringocystadenoma papilliferum

• Apocrine adenoma are always benign and excision is curative Clinical Variants
• None
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Epidemiology Syringocystadenoma papilliferum
• Rare
• Predominately affects children Introduction
Syringocystadenoma papilliferum is a benign apocrine neoplasm. These neo-
Pathophysiology plasms present clinically as crusting and often oozing papules or plaques most
• Benign neoplasm arising from apocrine commonly located on the head and neck. Histologically they are characterized
glands or pluripotential appendageal by wide papillary fronds, which extend above the surface of the epidermis. The
cells epithelium consists of oval to cuboidal cells with areas of decapitation and secre-
• Unknown etiology tion.
Clinical features Histological features

• 1–3 cm diameter 1. Invaginating cystic spaces open to skin surface
• Crusted, red warty plaque or nodule 2. Wide papillary fronds surfacing into epidermis
• Usually found on head and neck though 3. Frond bilayer consisting of basal cuboidal cells and apical columnar cells
other locations are reported 4. Dense core of lymphocytes and plasma cells within stroma
• May ooze malodorous serosanguinous 5. Decapitation and secretion
fluid
• Commonly found in conjunction with
nevus sebaceous of Jadassohn (up to one-
third of cases) 1
Special studies 3
• CEA+ 4
• GCDFP-15+ 2 5
• CK7+
2 Syringocystadenoma papilliferum
1. Hidradenoma papilliferum:
• Usually less than 1 cm in diameter
• Most commonly found on vulva
• Well-demarcated nodular appearance in the dermis, usually without epider-
mal connection
• Less plasma cells in fibrous papillary cores
2. Nipple adenoma:
• Endophytic lesion, often open toward the epidermal surface
• Wedge-shaped and consists of tubular elements covered by a double row of
epithelial cells
• Tubules are separated from one another by fibrous septa
Hidradenoma papilliferum Nipple adenoma

• Rarely evolves into a carcinoma
Clinical Variants
• None
44
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Hidradenoma
Introduction
Hidradenoma is a form of benign adnexal neoplasm that is a close relative of
poroma. It is usually characterized by cells with ample cytoplasm, and does
not commonly have a broad-based connection to the epidermis.
Hidradenomas can be either apocrine or eccrine lineage. The vast majority of
hidradenomas are believed to be of apocrine lineage.
Epidemiology
• Any age
Histological features • More prominent in women than men
1. Sharply circumscribed, non-encapsulated dermal tumor

2. Duct-like structures
Pathophysiology
3. Collections of cells with ample cytoplasm but uniform nuclei (larger than • Benign tumor with either apocrine or ec-
the nuclei of poroma) crine differentiation
4. Sclerotic stroma that may contain ectatic vessels
5. Cystic spaces may be present
2
1
4
5
3
Hidradenoma

1. Poroma: • Solitary dermal or subcutaneous nodule
• Granulation tissue-like quality stroma • Often skin-colored or blue-gray
• Two populations of cells, poroid and cuticular • Sometimes, appears as a cystic lesion and
2. Metastatic renal cell carcinoma: produce serous drainage
• Cells with ample eosinophilic cytoplasm • No anatomical preference
• Numerous blood vessels
Special studies
• None
Poroma Metastatic renal cell carcinoma

• Hybrid lesions with features of both hidradenoma and poroma can be
encountered, and the intermediate term poroid hidradenoma has been
applied in this setting
Clinical Variants
• None
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Cylindroma
Introduction
A benign adnexal neoplasm, with a characteristic histology that usually mani-
fests as nodules on the scalp.

• It may develop at any age but are most 1’. Dermal tumor without attachment to the epidermis
commonly in young adults, age 20–40 1. Basaloid cell islands in a jigsaw puzzle pattern
years 2. Two cellular population; outer layer composed of small, round cells with scant
• More common in women cytoplasm; inner layer composed of larger cells with more cytoplasm
3. Islands surrounded by sclerotic material and contain sweat ducts
Pathophysiology
• Familial cylindromatosis is inherited in
an autosomal dominant fashion, and the
responsible gene, CYLD, is located on 1’ 3 2
1 3
chromosome 16q12-13 2
Clinical features
• Cylindroma is a firm or hard raised 4 4
nodule, pink or bluish red in color, dome-
shaped Cylindroma
• Most of the time they are solitary lesions
that commonly involve the head and
neck, especially the scalp
• However, multiple lesions can be also Histological differential
seen (turban tumor) cover the entire
scalp, but they can also involve the face 1. Spiradenoma:
and upper body • Prominent presence of lymphocytes
• They are generally benign, but occasion- 2. Basal cell carcinoma:
ally may show local invasion and malig- • Peripheral palisading
nant degeneration • Cleft between tumor and stroma
• Mucinous stroma
Special studies • Necrosis
• Mitoses
• Immunohistochemical analysis: CK7,
CK8, CK18, CEA are positive
Spiradenoma Basal cell carcinoma

Clinical Variants • There are strong histochemical similarities between cylindromas and
spiradenomas, and they may coexist in the same individual
• Solitary • Cylindromas show an association with eccrine spiradenoma and tricho-
• Multiple sporadic epitheliomas in Brooke syndrome
• Multiple as part of Brooke-Spiegler
syndrome
46
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Apocrine hidrocystoma
Introduction
Apocrine hidrocystoma (AH) typically presents as translucent, skin-colored to
bluish cysts on the face and histologically as unilocular or multilocular cysts
lined by epithelial cells that demonstrate apocrine decapitation.
Epidemiology
Histological features • Occurs most commonly in middle-aged
1. Dermal cysts lined by two layers of epithelial cells or elderly individuals
2. Outer layer of myoepithelial cells and inner layer of columnar with decapita-
tion secretion Pathophysiology
• It arises from the apocrine secretory coil
Clinical features
1 • Translucent, skin-colored to bluish cyst
• 3–15 mm diameter
• Typically found on face, neck, and perior-
2 bital region
• Usually solitary lesion
• Unusual in children
Apocrine hidrocystoma Apocrine hidrocystoma
Special studies
Histological differential • AH is S-100 negative, PAS positive; ec-
crine hidrocystomas are typically S-100
1. Epidermal inclusion cyst: positive and PAS negative
• Cystic cavity filled with laminated keratin • AH expresses human milk-fat globulin
• Cyst lined by stratified squamous epithelium antigen while eccrine hidrocystomas do
not
Epidermal inclusion cyst

• May be associated with Schopf-Schulz-Passarge and Goltz syndrome
Clinical Variants
• None
47
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Mixed tumor
Introduction
Historically, mixed tumors of the skin, also known as chondroid syringoma,
included both eccrine and apocrine variants. They are distinct benign adnexal
neoplasms of the skin.
Epidemiology
• Rare Histological features
• More common in men 1. Well-circumscribed dermal or subcutaneous lobular tumor
2. Epithelial component: heterogeneous eccrine, apocrine, sebaceous, pilar,
Pathophysiology simple glandular, or squamous differentiation
• They are acquired hamartoma with 3. Stromal component: variable chondroid, mucinous, hyalinized, or osteoid
folliculosebaceous-apocrine or eccrine matrix
differentiation
Clinical features
• Solitary, slow-growing nodule that are
often misconstrued as cyst
• Commonly found in head and neck but
may also develop in the trunk or in axil- 1
lary or genital skin
Special studies
• CEA
Mixed tumor apocrine type Mixed tumor eccrine type
1. Cutaneous chondroma:
• Absence of tubular structures
• Found in distal extremities (mixed tumors are more common in the head and
neck)
• Prominent calcification
Chondroma

• Mixed tumor is benign and most lesions are treated by simple enucle-
ation. In contrast to mixed tumors of salivary origin, there is no need for
excision with wide margins.
Clinical Variants
• None
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Spiradenoma
Introduction
A spiradenoma is a benign adnexal tumor with areas of eccrine or apocrine
origin. Usually lesions appear as solitary, slow-growing, tender or painful,
reddish-brown or bluish intradermal nodule measuring 1–2 cm in diameter.
Epidemiology
Histological features • Mostly arises in young adults
1. Sharply demarcated basophilic dermal nodule (blue balls in dermis)
2. No epidermal connection Pathophysiology
3. Vascular stroma • It has either eccrine or apocrine differen-
4. A heavy diffuse lymphocytic infiltrate tiation
1,2
Clinical features
4
• Presents usually as a solitary dermal or
4 subcutaneous papule or nodule, 1–2 cm
3 in diameter, in a variety of hair bearing
locations
• Nodules are usually tender and maybe
painful
• Color may be reddish-brown or bluish
Spiradenoma Spiradenoma • Can simulate a vascular lesion
• Diagnosis may not be clear by clinical
examination and a biopsy is usually war-
Histological differential ranted
1. Cylindroma:
• Jigsaw puzzle
Special studies
• No lymphocytes • CEA may be positive
• Originates from the epidermis, demonstrates peripheral palisading
• Separation artifact (mucinous stroma)
Cylindroma Basal cell carcinoma

• Rarely, malignant progression may occur after benign lesions have been
present for several months or several years
• Spiradenomas may be seen in Brooke-Spiegler syndrome
• An autosomal dominant condition associated with spiradenomas, mul-
tiple cylindromas and trichoepitheliomas/trichoblastomas Clinical Variants
• Solitary
• Multiple
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Syringoma
Introduction
Syringomas are small flesh-colored papules that are classically found on lower
eyelids.

• Syringomas often appear during the 1. Well-defined superficial dermal tumor
third and fourth decades of life, although, 2. Numerous small ducts embedded in sclerotic stroma
they are by no means limited to this time 3. One or two layers of epithelial cells line the lumens of the ducts containing
period and are commonly found in any amorphous debris
age group at or after puberty 4. Tadpole-shaped ducts
• They are twice as common in women
• More common in patients with Down 3
syndrome
2
Pathophysiology 1
2 4
4
• Syringomas arise from eccrine sweat

glands
Clinical features
• Syringomas are small, skin-colored, often Syringoma Syringoma
bilateral, firm papules. They are usu-
ally small and no larger than 1–2 mm in Histological differential
diameter
• Syringomas may occur at any site on the 1. Microcystic adnexal carcinoma:
body but they mostly occur in the perior- • Large
bital area, especially the eyelids • Deep infiltration of reticular dermis, subcutaneous fat, skeletal muscle, and
• They can also be found on the cheeks, cutaneous nerve
axillae, vulva, penis and abdomen. The • Follicular differentiation
lesions on the vulva and penis are usually 2. Desmoplastic trichoepithelioma:
solitary • Fragments of keratin in the lumina
• Eruptive syringomas most commonly • Dystrophic calcification
involve the trunk but may involve the • Rims of fibrous tissue around the neoplastic collections
extremities, including palms and soles • More frequent foreign body giant cell reaction to extruded keratin
Special studies
• None
Microcystic adnexal carcinoma Desmoplastic trichoepithelioma

• Rarely, syringoma will display cells clear, vacuolated cytoplasm. This is
caused by accumulated glycogen and is known as clear cell syringoma
and are associated with diabetes mellitus
Clinical Variants
• Eruptive syringoma
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Poroma
Introduction
Poroma is a benign adnexal neoplasm derived from acrosyringium. Histopath-
ologically, poromas are traditionally subcategorized into three main variants
based on their location in relation to the epidermis: hidroacanthoma simplex,
poroma, and dermal duct tumor. The malignant counterpart of a poroma is Epidemiology
known as porocarcinoma. • Onset of poromas is typically in adult-
Histological features hood but they can develop at any age
• No known gender or ethnic predisposi-
1. Well circumscribed tion
2. Connects with the epidermis
3. Mixture of small cuboidal cells with monomorphous ovoid nuclei (poroid Pathophysiology
cells) and larger cells with an eosinophilic cytoplasm (cuticular) • Poromas are viewed as proliferations of
4. Ductal structures, consisting of tubules lined by a dense eosinophilic cuticle the acrosyringium, which is the intraepi-
5. Highly vascularized stroma, corresponding to a clinical picture similar to dermal portion of the sweat duct
pyogenic granuloma
Main subtypes: Clinical features
• Hidroacanthoma simplex represents a pattern of poroma in which tumor • Most commonly present as a solitary,
cells are confined to the epidermis slow-growing, papule/plaque or nodule
• Poroma involves both the epidermis and dermis. It consists of aggregates of on the soles or palms
uniform-looking basaloid cells radiating from the base of the epidermis into • May be skin-colored, pigmented, or
the dermis vascular in appearance, and sometimes
• Dermal duct tumor is confined to the dermis. It consists of poroid cells exhibiting surface erosion or ulceration
forming several sharply circumscribed dermal nodules • It may be itchy or painful
5
Special studies
2 • None
1 1 4
3
Poroma
1. Seborrheic keratosis:
• No ductal structures
• Horn pseudocysts
• Peripheral palisading
• Stromal retraction
Seborrheic keratoses
Basal cell carcinoma

• Poromas commonly display small collections of necrosis cells and the
cause is unknown. Although necrosis en masse is suggestive of a ma-
lignancy (due to rapid growth beyond the capacity of perfusion), such
occurrence in poromas is an exception
Clinical Variants
• None
51
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Sweat Gland Neoplasms • Malignant tumors
Adenoid cystic carcinoma
Introduction
Adenoid cystic carcinoma (ACC) is a rare malignant neoplasm associated with
secretory glands throughout the body, including the salivary glands, respiratory
tract, breast, skin, uterine cervix, thymus, and prostate gland. Commonly pre-
Epidemiology sented as a slow-growing mass, diagnosis is made histologically by biopsy and
• Female to male ratio of 3:2 with typical identification of their cribriform, tubular, or solid growth patterns.
onset between 40–60 years of age
• Unknown etiology Histological features
• Risk factors unknown 1. Monomorphic basaloid cells with compact nuclei and a small amount of sur-
rounding cytoplasm
Pathophysiology 2. Arranged in elongated nests, tubules and/or cords
• ACC arises by neoplastic transformation 3. Cribriform and tubular areas
of glandular epithelia stem cells. Initiat- 4. Abundant basophilic mucin in cysts
ing factor unknown
Other features:
Clinical features • Perineural infiltration
• Slow-growing mass invading dermis and
subcutaneous tissue
4
• Typically found on scalp and chest area
• High incidence of local recurrence
• Perineural involvement and distant me-
3
tastases in later stages of disease
Special studies 1
2
• ACC is immunoreactive with epithelial

membrane antigen (EMA) and carcino- Adenoid cystic carcinoma Adenoid cystic carcinoma
embryonic antigen
1. Adenoid basal cell carcinoma:
• Multilinear differentiation
• Stromal retraction
Adenoid basal cell carcinoma

• Post-treatment, patients should be closely followed due to high recur-
Clinical Variants rence rate
• None
52
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Microcystic adnexal carcinoma
Introduction
Microcystic adnexal carcinoma (MAC) is a rare cutaneous malignant tumor
that is locally invasive and often presents with perineural invasion

1. Biphasic pattern (sweat duct-like and pilar) • Typically seen in young or middle-aged
2. Tadpole-shaped ducts adults
3. Horn cysts • More prominent in women than men
4. Sclerotic stroma • Risk factors: UV light exposure
5. Deeply invasive, involves dermis and subcutis (bottom heavy)
Pathophysiology
• It is a carcinoma that differentiates to-
1 ward sweat glands and hair follicles
1
2 4
Clinical features
3 • Slow growing
• Indurated, firm plaque or nodule
• Yellow to flesh-colored
• Predilection for face, head, and neck
5 (most commonly on the upper lip)
Microcystic adnexal carcinoma • Typically presents on the left side
Special studies
Histological differential • CEA, EMA, CK7
1. Syringoma:
• More superficial
• Small
• No perineural extension
• No lymphoid aggregation
2. Desmoplastic trichoepithelioma:
• More superficial
• No perineural extension
• Rare lymphoid aggregation
Syringoma
Desmoplastic trichoepithelioma

• MAC is a low-grade form of adnexal carcinoma
• Local recurrence common
• Metastasis rare
• Perineural invasion and lymphoid aggregates sometimes are seen in
MAC
Clinical Variants
• None
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Extramammary Paget’s disease
Introduction
Extramammary Paget’s disease (EMPD) is an uncommon intraepithelial adeno-
carcinoma, which primarily affects the apocrine-bearing skin.
1. Neoplastic cells with large nuclei and abundant amphophilic cytoplasm
2. Single cells or clusters more numerous in basal layer
Epidemiology 3. Glandular structures commonly seen
• EMPD represents 1–2% of primary Other features:
neoplasms of the vulva and anogenital • Tumor cells with propensity to track along skin appendages
region. Axillae, eyelids and external audi-
tory canal rarely may be involved
• Women are commonly affected. Most 1
patients are above the age of 60
2
Pathophysiology
2
• It is thought to arise from pluripotential
stem cells in the epidermis
• It can be associated with an underlying
adenocarcinoma of skin appendages or
Bartholin’s glands Extramammary Paget’s disease Extramammary Paget’s disease
• EMPD needs to be distinguished from
secondary pagetoid colonization of the
epidermis by a noncutaneous carcinoma,
mainly from the bladder or the bowel
Clinical features
• Well-demarcated erythematous scaly
patches and plaques, which may be ulcer-
ated CK7 staining
• Intractable pruritis is a common present-
ing symptom
1. Pagetoid squamous cell carcinoma in situ:
Special studies • CK5/6+, P63+, CK7–, CEA–, GCDFP15–
2. Melanoma in situ:
• Immunohistochemical analysis: CK7+, • S-100+, HMB-45+, CK7–, CEA–, GCDFP15–
CAM5.2+, EMA+, pCEA+, GCDFP15+,
HER2+, stains for mucin are positive in
70% of the cases
Pagetoid squamous cell Melanoma in situ

carcinoma in situ

• Paget cells can contain cytoplasmic melanin pigment, a feature that
Clinical Variants should not imply melanocytic differentiation
• None
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Hidradenocarcinoma 1
Introduction
Hidradenocarcinoma is a rare malignant carcinoma often appearing on the
3
face and extremities, and sometimes trunk. Most cases develop de novo and
rarely in association with an existent hidradenoma. Clinically, it is very hard to
diagnose due to the variations of its presentation. Epidemiology
• Common in middle-aged to elderly
1. Sheets of cells with glycogen-containing pale cytoplasm and distinct cell Pathophysiology
membranes • Most tumors have apocrine differentia-
2. Cytoplasmic vacuoles tion
3. Focal necrosis
Clinical features
2
• Usually presents as an ulcerated reddish
nodule in elderly
Special studies
• Cam5.2+, EMA decorate the luminal
border of ductal structures
Hidradenocarcinoma
1. Porocarcinoma:
• Lack of clear cell change
2. Sebaceous carcinoma:
• Sebaceous differentiation (vacuolated cells)
Sebaceous carcinoma Porocarcinoma

• Aggressive course, with distant metastasis to lymph nodes, bones, and
lungs
• Wide local excision with 2 cm margins is the treatment of choice
Clinical Variants
• None
55
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Porocarcinoma
Introduction
Porocarcinoma is a rare aggressive malignant adnexal neoplasm of sweat gland
duct.
Epidemiology
• Porocarcinomas represent 0.005–0.01%
of all malignant cutaneous tumors
• It is primarily a tumor of elderly adults,
1 2
50–80 years of age, although it has been
reported in young adults
• There is no predilection for either gender
Pathophysiology
• The etiology of theses tumors remains Histological features
unknown, they can arise de novo or in a 3
pre-existing benign poroma 1. Cords and lobules of invasive pleomor-
phic basaloid cells 3
Clinical features 2. Ducts lined by cuboidal epithelial cells

and eosinophilic luminal cuticle
• The lesions present as nodules or infil- 3. Frequent mitoses and sometimes ne-
trated plaques with or without verrucous, crosis
ulcerative or polypoid characteristics 4. Squamous differentiation and clear cell
• Most frequent sites of involvement are changes Porocarcinoma
the lower extremities followed by the
trunk and head Histological differential
• Tumors vary in size from 1 cm to 10 cm.
A long standing history is often encoun- 1. Squamous cell carcinoma:
tered • No evidence of ductal differentiation
• The incidence of lymph nodes metastasis • No poroid cells
and distant metastasis are 20% and 11%, 2. Poroma:
respectively. Recurrence rate after exci- • Well circumscribed and symmetrical
sions 20% • No atypia
Special studies
• Immunohistochemical analysis: Ductal
differentiation can be highlighted by Squamous cell carcinoma
EMA and CEA
Poroma

• Ducts lined by cuboidal cells and eosinophilic cuticle help to differenti-
Clinical Variants ate porocarcinoma from other malignant tumors
• None
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TUMORS OF FIBROUS TISSUE
Benign Tumors • Nodular fasciitis
Introduction Epidemiology
Nodular fasciitis is a benign reactive proliferation of fibroblast-like cells that ap- • Common among soft tissue mass lesions
pears as a well-circumscribed, subcutaneous, fascial or intramuscular nodule. • Affects all age groups but more often
young adults
Histological features • Intravascular fasciitis and cranial fasciitis
are rare
1. Spindle-shaped to plump fibroblasts and myofibroblasts in a haphazard ar-
• Intravascular fasciitis is found mostly in
rangement (“tissue culture appearance”) embedded in a mucinous stroma
persons under 30 years of age
2. Cells with prominent oval nuclei and fine chromatin pattern
• Cranial fasciitis develops predominantly
3. Lymphocytes and extravasated red cells are also seen
in infants under 2 years of age
Other features: • No sex predilection but cranial fasciitis is
• Typical mitoses are common more frequent in boys
• Some cells may have a ganglion like appearance
• Capillaries with plump endothelial cells Pathophysiology
• Ossifying fasciitis shows areas with osteoid metaplasia
• Some patients with nodular fasciitis re-
port trauma to the site of the lesion, but
1,2 the majority do not
• Birth trauma may be a factor in the gen-
esis of cranial fasciitis
1,2
3
Clinical features
• Most commonly affects young to middle-
3 aged adults in the upper extremities
• Cranial fasciitis is a variant found in chil-
Nodular fasciitis Nodular fasciitis dren; arises in deep tissues of the scalp
and involves cranium
Histological differential • Lesions may grow quickly to >5 cm in
diameter
1. Fibrosarcoma:
• Self-limited process
• Proliferation of atypical fibroblasts arranged in a herringbone pattern. No
mucinous stroma
2. Pleomorphic sarcoma (malignant fibrous histiocytoma):
Special studies
• Neoplasms composed of pleomorphic cells of different sizes and shapes • Immunoperoxidase studies: cells are
positive for smooth muscle actin,
muscle-specific actin, vimentin, KP-1;
negative for desmin and S-100 protein
• Ganglion cells are only positive for
vimentin
Fibrosarcoma Malignant fibrous histiocytoma

• Nodular fasciitis can become very large and recur, especially in areas
like the head and neck
• Cells of nodular fasciitis produce tyrosine kinase, transforming growth
factor β, interferon, and tumor necrosis factor
Clinical Variants
• Florid reactive periostitis or fibro-
osseous pseudotumor of the digits
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Dermatofibroma
Introduction
Dermatofibromas (DF), also known as benign fibrous histiocytomas, are com-
mon cutaneous nodules of unknown etiology. There are a number of histologic
subtypes. Tumors that grow deeply into the fat underlying the skin do have the
Epidemiology potential for aggressive growth and local recurrence.
• Dermatofibroma is a very common lesion
and may develop at any age Histological features
• There is a predilection for the extremities, 1. Well-circumscribed neoplasm that usu- 2 1
3
particularly the lower of young adults ally spares the papillary dermis and
• There is a female predominance subcutaneous tissue and is perpendicular
to the epidermis 5
Pathophysiology 2. Epidermal hyperplasia with flattened
• It is controversial whether it is an inflam- “tabled rete ridges” and hyperpigmenta-
matory or neoplastic process tion of the basal layer
• Dermatofibroma has been reported 3. Follicular (simulating a basal cell carci-
following local injuries such as trauma, noma) and sebaceous induction
insect bites, or folliculitis, suggesting an 4. Fibroblast of different size and shape and
inflammatory etiology multinucleated histiocytes in many cases
4
• By contrast, some examples have been 5. Prominent kelloidal collagen at the
reported to be clonal, supportive of a periphery
neoplastic etiology Other features:
• Hemosiderin in the aneurysmal variant
Clinical features • Histological variants: aneurysmal/he- Dermatofibroma
• Dermatofibromas are round or ovoid, mosiderotic dermatofibroma, cellular
firm dermal nodules dermatofibroma, deep fibrous histiocytoma, atypical fibrous histiocytoma/
• Usually less than 1 cm in diameter dermatofibroma with monster cells and sclerotic DF
• It preferentially develops on the lower
limbs Histological differential
• Usually a dusky brown color but aneu- 1. Dermatofibrosarcoma protuberans:
rysmal variants may be red, and tumors • Large and poorly circumscribed, parallel to the epidermis
with abundant lipid can be cream/yellow • Bundles of collagen arranged in a storiform pattern and trapping subcutane-
• Most often solitary ous fat
• Cells with wavy nuclei in association with delicate fibrillary bundles
• CD34 positive
2. Neurofibroma:
• Spindle cells with wavy nuclei admixed with a vari-
able number of mast cells
• Mucinous stroma
• No keloidal collagen
• Immunoreactive for S-100 protein and neurofila-
ment
Dermatofibrosarcoma protuberans Neurofibroma
Special studies
• Immunohistochemistry: cells are usually
positive for factor XIIIa • They often show a characteristic central white, scar-like patch on derma-
toscopic examination, and a delicate pigment network at the periphery
• Many lesions demonstrate a “dimple sign,” where the central portion
puckers as the lesion is compressed on the sides. They generally do not
change in size
• Cellular DF may be CD34 positive
Clinical Variants
• None
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Superficial fibromatosis
Introduction
Fibromatosis have been defined as a “group of non-metastasizing fibrous tu-
mors which tend to be locally aggressive and recur after surgical excision”.
The “fibromatosis” include entities such as palmar and plantar fibromatosis,
and Peyronie’s disease of the penis, and knuckle pads. Epidemiology
Histological features • May occur in childhood or be acquired in
adulthood
1. Hypercellular lesions composed of fusiform fibroblasts with vesiculous • Some patients may have more than one
nuclei of fibromatosis at the same time
2. Stroma with moderate amount of collagen
Other features:
Pathophysiology
• In early stages mitotic figures can be seen • Proliferation of well-differentiated fibro-
blasts, an infiltrative growth pattern, and
aggressive clinical behavior with frequent
local recurrence
1
2 Clinical features
2
• Plantar fibromatosis: young to middle-
3 aged adults, thick sole may interfere with
walking
1
• Palmar fibromatosis (Dupuytren’s
contracture): older males, often develops
Fibromatosis Fibromatosis clinically chord-like bands on the palms
with flexion contraction
Histological differential • Penile fibromatosis (Peyronie’s disease):
middle-aged to older adult males slowly
1. Dermatofibrosarcoma protuberans: develop fibrous thickening of penis often
• Infiltrative neoplasms with monotonous cells in a storiform pattern extend- with dorsal curvature of the penis with
ing into the subcutaneous fat and producing a honeycomb appearance pain
2. Leiomyomas: • Knuckle pads affects dorsum of the
• Centered in reticular dermis but may extend into subcutaneous fat hands at the interphalangeal joints affect-
• Fascicles of smooth muscle and collagen ing mostly young adults and middle-aged
Special studies
• Immunohistochemical studies demon-
strate that the neoplastic cells are positive
for vimentin, smooth muscle actin and
some positivity for β-catenin
Dermatofibrosarcoma protuberans Leiomyoma
Important Things To Know Clinical Variants

• Multiple fibromatoses are seen in Gardener’s a syndrome • Plantar fibromatosis
• Treatment is mainly surgical • Palmar fibromatosis
• Knuckle pads
• Peyronie’s disease
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Malignant Tumors • Fibrosarcoma
Introduction
A fibrosarcoma is a malignant tumor of fibroblasts with no other cellular differ-
entiation. The greater the cellularity and the number of mitotic figures, the more
aggressive the neoplasm. The most aggressive fibrosarcomas can metastasize,
especially to the lungs via blood stream.

• The incidence of this tumor is difficult to 1. Interlacing fascicles of spindle cells in a “herringbone pattern”
assess because it is mostly a diagnosis of 2. Scant cytoplasm and elongated hyperchromatic nuclei
exclusion 3. Meshwork of collagen and reticulin between cells
• It probably accounts for 1–3% of adult Other features:
sarcomas • Mitotic figures
• Classical fibrosarcoma is most common • Histologic variants: sclerosing epithelioid fibrosarcoma, fibrosarcoma with pali-
in middle-aged and older adults saded granuloma-like bodies (giant rosettes), and inflammatory fibrosarcoma
• Congenital or infantile fibrosarcoma is
present at birth or develops within the
first year of life
• The sex incidence is equal 1
2
Pathophysiology 3
• Some arise in the field of previous thera-
peutic irradiation, and rarely in associa-
tion with implanted foreign material
• Thermal burns, radiation therapy may Fibrosarcoma Fibrosarcoma
lead to cutaneous fibrosarcomas
• Congenital-infantile fibrosarcoma
presents with a translocation t(12;15) Histological
(p13;q25) leads to ETV6–NTRK3 gene differential
fusion 1. Malignant fibrous histiocytoma:
• Partial fibroblastic and histiocytic
Clinical features differentiation
• Fibrosarcoma presents as a mass with or • Collagen production
without pain • Multinucleated cells usually present
• In specific sites local symptoms relate to 2. Nodular fasciitis:
the effects of a mass • Involves myofibroblasts as well as Malignant fibrous histiocytoma
• Affects young to middle-aged adults fibroblasts
• Usually located in lower extremities, fol- • Common in the upper extremities
lowed by the upper extremities, trunk, • May express KP-1
and then the head and neck region
• Hemorrhage and necrosis can be seen in
high grade tumors
Special studies
Nodular fasciitis
• Tumor cells express vimentin but not
desmin, S-100 protein, or smooth muscle
actin Important Things To Know
• Congenital-infantile fibrosarcoma: less aggressive than adult-type. His-
tological appearance is similar
• Tumors with the histological features of adult fibrosarcoma may arise in
dermatofibrosarcoma, solitary fibrous tumor and in well-differentiated
liposarcoma, either in the primary or in recurrence, as a reflection of
tumor dedifferentiation
Clinical Variants
• Congenital or infantile fibrosarcoma
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Dermatofibrosarcoma
protuberans
Introduction
Dermatofibrosarcoma protuberans (DFSP) is a locally aggressive sarcoma of
low-intermediate malignancy that favors young to middle-aged adults. Lesions
that are present at birth or with an onset during childhood have been report-
Epidemiology
ed. DFSP occurs on the trunk in 50–60% of patients, the proximal extremities • DFSP typically presents during early or
in 20–30%, and the head and neck in 10–15%. There is a predilection for the middle adult life However, some tumors
shoulder or pelvic region. start during childhood and become only
apparent during young adulthood
Histological features • Male predominance
1. Poorly circumscribed neoplasm which has a parallel orientation to the Pathophysiology

epidermis
• Unique cytogenetic abnormalities recip-
2. Affects dermis and extends into the subcutaneous tissue
rocal t(17;22) translocations
3. Has a characteristic honeycomb pattern with trapping of the subcutaneous
• DFSP arises from the dermis and invades
tissue
deeper subcutaneous tissue (fat, fascia,
4. The cells are fairly uniform
muscle, bone)
Other features: • The cellular origin of DFSP is uncertain
• Mitotic figures are low-to-moderate (less than 5/10 HPF) • A history of precedent trauma is present
• Tumor cells tightly encase skin appendages without destroying them in 10–20% of all patients
• Some tumors have a prominent myxoid matrix • DFSP may also arise in surgical scars,
• In some tumors, multinucleated cells are seen (giant cell fibroblastoma) burns and vaccination sites
1
Clinical features
• It presents as a slowly growing, asymp-
4 tomatic, skin-colored, indurated plaque
3 • Violaceous to red–brown nodules mea-
2 suring from one to several centimeters in
diameter
• On palpation, the lesion is firm and at-
tached to the subcutaneous tissue
• Accelerated growth during pregnancy
Dermatofibrosarcoma protuberans
• Most common locations: trunk and
proximal extremities
1. Fibrosarcoma: Special studies
• Highly pleomorphic cells • Immunostaining pattern of DFSP: CD34-
• Herringbone pattern positive, factor XIIIa-negative
2. Dermatofibroma (especially deep penetrating variants):
• Extension into the subcutaneous tissue
• Keloidal collagen and multinucleated
histiocytes
• Positive staining for factor XIIIa and nega-
tive staining for CD34 in most cases
Fibrosarcoma
Dermatofibroma
• Treatment of choice: Mohs micrographic surgery
• Multiple local recurrences appear to lead to the evolution of a more ag-
Clinical Variants
gressive tumors and the development of a metastatic disease • Bednar tumor
• Myxoid DFSP
• Giant cell fibroblastoma
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Atypical fibroxanthoma
(superficial malignant fibrous
histiocytoma)
Introduction
Epidemiology Atypical fibroxanthoma is a low-grade sarcoma that occurs in sun-damaged skin
• Predominance in elderly males of the head and neck of elderly patients. Atypical fibroxanthoma is considered to
• A few in children with xeroderma pig- be a superficial form of malignant fibrous histiocytoma.
mentosum
• A rare variant can develop in non-sun- Histological features
damaged skin of the trunk or extremities 1. Poorly circumscribed neoplasm com- 2
in younger patients 1
posed of pleomorphic cells, which affect
the dermis and sometimes extend into
Pathophysiology the subcutaneous tissue
• It has been regarded as a proliferative 2. Solar elastosis
mesenchymal, possibly fibrohistiocytic, 3. Atypical bizarre spindle-shaped cells
response to a variety of cutaneous inju- and multinucleated cells
ries Other features:
• In older patients there is often a history • Often the epidermis is ulcerated
of prolonged actinic exposure, but lesions • Numerous mitotic figures
may also develop at sites of irradiation • Large atypical cells with abundant pale- 3
and even trauma staining vacuolated cytoplasm 3
• This tumor may also develop in renal • A rare variant with scattered osteoclast-
transplant recipients like multinucleated giant cells has been
• A less aggressive behavior has been as- reported Atypical fibroxanthoma
sociated to the absence of ras oncogene
mutations in AFX, whereas MFH has
both H- and K-ras gene mutations
• Neoplasm that extend into the subcuta-
neous tissue have a higher incidence of
recurrence 1. Leiomyosarcoma:
• Lesions may regress spontaneously or • Nuclear atypia
after incomplete removal • Mitotic activity of 1 or more per 50 HPF
• Necrosis
Clinical features • Positive SMA
2. Desmoplastic melanoma:
• It usually presents as a solitary rapidly • Focal lymphoid aggregate
growing nodule • Positive S-100 and P75 but negative
• Gray to pink or red dome-shaped nodule Melan-A and HMB-45
that measures from 1–2 cm in diameter Leiomyosarcoma
on the head or neck of the elderly
• Secondary changes include serosanguin-
eous crusts and ulceration may occur
Important Things To
Special studies Know
• Both the spindle-shaped cells and the • Features that may portend a
histiocyte-like cells react positively for more aggressive behavior include
vimentin vascular invasion (the most reli-
• The large histiocyte-like cells react posi- able feature), extension into deep
tively for α1-antichymotrypsin, CD68, tissues and tumor necrosis which
procollagen and CD10 is more prominent in MFH Desmoplastic melanoma
• Negative for Pankeratin and S-100 • Atypical fibroxanthomas should
be treated by wide local excision,
Mohs technique may be of benefit
in cases on the head and neck
Clinical Variants
• None
62
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TUMORS OF FAT
Lipoma
Introduction
Lipoma is a benign tumor composed of mature adipocytes and is the most
common soft tissue mesenchymal neoplasm in adults.

1. Lobules of mature adipocytes, surrounded by a delicate connective tissue • Most common between the ages of 40
2. Cells are identical to the surrounding adipose tissue and 60 years
• More frequent in obese individuals
• Rare in children
• Approximately 5% of patients have mul-
tiple lipomas
1 2 Pathophysiology
• Unknown, however, lipomas are more
common in obese individuals
Clinical features
Lipoma
• Lipomas are usually painless, except for
larger ones that can elicit pain if they
Histological differential compress peripheral nerves
• Superficial lipomas are generally smaller
1. Angiolipoma: (<5 cm) than the deep seated ones (>5 cm)
• Prominent blood vessels • Lipoma arborescens is a fatty infiltra-
2. Spindle cell lipoma: tion of subsynovial connective tissue in a
• Prominent spindle cells in mucinous stroma in adipose tissue large joint, usually the knee. Affects older
patients, usually male, associated with
joint trauma, degenerative joint disease
and chronic arthritis
• Conventional lipoma can arise within subcu-
taneous tissue (superficial lipoma) or within
deep soft tissues (deep lipoma) or even on
the surfaces of bone (parosteal lipoma)
• Deep-seated lipomas that arise within or
between skeletal muscle fibers are called
intramuscular or intermuscular lipomas,
Angiolipoma Spindle cell lipoma respectively
Special studies
• Mature adipocytes stain for vimentin,
S-100 protein and leptin
• Imaging studies show a homogeneous
soft tissue mass that is isodense to the
Important Things To Know subcutaneous tissue and demonstrates fat
saturation
• The infiltrating intramuscular lipoma has a higher local recurrence
rate, therefore total removal of the involved muscle or a compartmental
resection has been suggested for these infiltrating tumors in order to
minimize local recurrence
Clinical Variants
• Conventional lipoma
• Deep-seated lipoma
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Angiolipoma
Introduction
Angiolipomas are subcutaneous tumors of blood vessels and fat.
Epidemiology 1. Thin fibrous capsule with incomplete fibrous septa
• Angiolipomas comprise 10% of tumors of 2. Variable proportion of mature adipose and blood vessels
the fat 3. Fibrin micro thrombi
• Occur at young age group
Cellular angiolipoma:
Pathophysiology • Vascular component comprises the bulk of the lesion
• Angiolipomas have normal karyotype,

and for this reason they have been re- 2
garded as a hamartoma of blood vessels 2
and fat, rather than a true tumor of fat
3
• A family history is found in about 10% of
cases 1
Clinical features 1
• Painful lesions occur most commonly in Angiolipoma

the forearm or on the trunk Angiolipoma
• Usually multiple

• None 1. Lipoma:
• No fibrin thrombi
2. Hemangioma:
• Capillaries radiate out from a central large vessel but in angiolipoma, capillar-
ies are located peripherally
Lipoma Hemangioma

• Angiolipoma is a painful lesion and that appears to be related to the
Clinical Variants vascularity of the tumor
• None
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Nevus lipomatosus superficialis
Introduction
Nevus lipomatosus superficialis (NLS) is an uncommon form of connective tis-
sue nevus, manifest principally by the deposition of fatty tissue in the dermis.

1. Polypoid lesion made up of lobules of mature fat in variable quantities in • Typically, the lesions present in early
superficial dermis childhood or adolescence
2. Increased number of small blood vessels around fatty lobules • Such lesions have been described as
3. Areas of loose fibrous tissue pedunculated lipofibroma
• In all types of nevus lipomatosus the sex
Other features: incidence is equal
• Diminished elastic fibers and reduced numbers of epidermal appendages
Pathophysiology
3 • The pathogenesis is unknown
2
1
Clinical features
• In classical form, it is characterized by
multiple papular, polypoid, or plaque-like
lesions, up to 2 cm in diameter, which
almost always arise unilaterally on the
posterior surfaces of the buttocks, upper
Nevus lipomatosus superficialis Nevus lipomatosus superficialis
thighs or lower back
• The papules or plaques, varying from
Histological differential skin-colored to yellow, are characteristi-
cally broad based and may show superfi-
1. Fibroepithelial polyp: cial comedone formation
• Papillary, fibrovascular cores covered by squamous epithelium
• May have ischemic necrosis due to torsion Special studies
• None
Skin tag

• A solitary form, usually seen in adults, shows a predilection for the
same sites or occurs elsewhere and is more likely to represent a variant
of fibroepithelial polyp or skin tag
Clinical Variants
• Solitary form NLS
• Extensive and diffuse NLS
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TUMORS OF SMOOTH MUSCLE
Benign Neoplasms • Leiomyoma
Epidemiology Leiomyoma (superficial leiomyoma/
• Uncommon
leiomyoma cutis/superficial
benign smooth muscle tumor)
• Females more
often affected
than males
• Congenital le- Introduction
sions are prob- Leiomyomas are benign dermal tumors that are subclassified into three cat-
ably variants of egories according to their location. Piloleiomyomas arise from the erector pili
smooth muscle muscles; genital leiomyomas arise in the dartos, vulvar, or mammillary smooth
hamartoma muscles; and angioleiomyomas arise in the smooth muscle of blood vessel walls.
Pathophysiology 1. Neoplasm composed of uniform smooth
• Leiomyomas arise from smooth muscle cells muscle cells with eosinophilic cytoplasm,
• Most patients with multiple leiomyomas oval nuclei with blunt ends “cigar”-shaped
have germline mutation of the fumarate
hydratase gene Piloleiomyomas
• Usually centered in reticular dermis but
Clinical features may extend into surrounding fat tissue,
or subcutis
• Piloleiomyomas: Mostly seen in adults, • Poorly circumscribed fascicles of smooth
solitary or multiple, painful, firm, reddish- muscle and collagen (unencapsulated
1
brown papules or nodules. Usually 1–2 cm and infiltrative) often involving hair fol-
in diameter. Multiple nodules often seen licles and adnexal glands
as plaques, linear, grouped, or in a derma- 1
tomal pattern. Appear more often in lower Genital leiomyomas
extremities and trunk (especially shoulder) • Well circumscribed and centered in
• Genital leiomyomas: Often solitary, pain- subcutaneous tissue
less, well-circumscribed subcutaneous nod- • Spindle-shaped or epithelioid cells, may
ules. Usually <2 cm in diameter but may be have a pseudocapsule, focal calcifica-
tions, or stromal myxoid change. Few Leiomyoma
as large as 15 cm in diameter. Appear on
vulva, penis, scrotum, nipple and areola mitotic figures may be present
1. Dermatofibroma:
• Less fascicular
• Rounder and more polymorphic cells
• Foamy macrophages may be present
2. Leiomyosarcoma:
Dermatofibroma • Presence of nuclear atypia
Leiomyosarcoma • Mitotic figures, some of them atypical
• Necrosis
Special studies
• Immunohistochemistry with antibodies
against smooth muscle actin or desmin Important Things To Know
• Differentiation between piloleimyomas and genital leiomyomas is
Clinical Variants significant for prognosis: patients with multiple dermal leiomyomas ex-
perience recurrence at 50% rate, while patients with genital leiomyomas
• Piloleiomyoma usually remain disease-free up to 5 years of follow up
• Genital leiomyoma
• Angioleiomyoma
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Malignant Tumors • Leiomyosarcoma
Introduction
Leiomyosarcoma is a malignant tumor composed of cells showing distinct
smooth muscle differentiation. Primary cutaneous leiomyosarcomas are infre-
quent tumors that may arise in the dermis or subcutaneous tissue. Secondary
leiomyosarcomas are exceedingly rare. Dermal and subcutaneous lesions have
a different biological behavior.
Histological features 1
1. Flattening of the rete ridges Epidemiology
2. Interlacing fascicles of cells 5
• Soft tissue leiomyosarcoma usually oc-
3. Elongated spindle-shaped cells with 6
5 curs in middle-aged or older persons,
eosinophilic cytoplasm and eccentric, although it may develop in young adults
blunt (cigar-shaped) nuclei and even in children
4. Multinucleated cells • Predilection for the extensor surfaces of
5. Small lymphoid aggregates the extremities, and to a lesser extent the
6. Infiltrative margins scalp, and trunk
7. Moderate to severe cytological atypia and necrosis • There is a male predominance
3 3
Other features:
• More than 5 mitoses/10 high-power fields (HPF)
2 Pathophysiology
2 • Primary cutaneous leiomyosarcomas are
4
infrequent tumors that may arise in the
Leiomyosarcoma 2
dermis or subcutaneous tissue
• Dermal tumors presumably arise from
the erector pili muscles, except for scrotal
Histological differential 7
lesions, which derive from the dartos
1. Dermatofibrosarcoma protuberans: muscle
• Widely infiltrative and monotonous cells • Subcutaneous leiomyosarcomas arise
• Storiform pattern from the smooth muscle in vessel walls
2. Leiomyomas: • The most frequent genomic alterations
• Centered in reticular dermis but may extend into surrounding fat, tissue, or in leiomyosarcomas involve losses in the
subcutis 13q4–q21 region
• Poorly circumscribed fascicles of smooth muscle and collagen
Clinical features
• Presents as a mass lesion. The tumors
vary in size from 0.5–3 cm or more in
maximum diameter. Subcutaneous ex-
tension is present in two-thirds of cases
• Pain or tenderness is present in some
• Other symptoms depend on location
Special studies
Dermatofibrosarcoma protuberans Leiomyoma • Immunoperoxidase preparations show
the presence of vimentin, smooth muscle
actin, and H-caldesmon

• Dermal leiomyosarcomas may recur locally in up to 30% of cases. The
recurrence rate seems to be lower when wide surgical excision is carried
out initially
• Subcutaneous leiomyosarcomas tend to be slightly larger and more
circumscribed. They have a greater tendency for local recurrence
(50–70%), and metastases to lung, liver, and other sites
Clinical Variants
• Retroperitoneal sarcomas
• Limb sarcomas
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NEURAL TUMORS
Nerve Sheath Tumors • Neurofibroma
Introduction
Neurofibromas (NF) can be classified either as solitary or multiple. Solitary NF
are incidental findings and are usually not associated with systemic manifesta-
tions. Multiple NF on the other hand may be seen in patients with neurofibro-
matosis or von Recklinhausen’s disease.
Epidemiology 1. Well-circumscribed, non-encapsulated
• Solitary cutaneous lesions are common lesions involving the dermis and subcutane- 1
in young adults and have no gender ous tissue
preference 2. Composed of spindle cells with wavy nuclei
• Plexiform NF almost always indicate NF1 and indistinct cytoplasmic borders
3. The stroma has variable amounts of mucin-
Pathophysiology containing mast cells
• Neurofibromas are a complex prolifera- Other features: 2
tion of neuromesenchymal tissue, which • Small nerve fibers 3
includes Schwann cells, perineural cells, • Varying amounts of collagen are pres-
endoneural cells, and mast cells ent and sometimes there is a marked
• With NF1 associated neurofibromas, myxoid stroma
genetic studies have indicated mutations in
the NF1 gene cause inactivation of the neu-
rofibroma protein or haplo insufficiency
Clinical features Neurofibroma

• Clinically, neurofibromas are most com-
monly seen in the second and third decade Histological differential
of life, they are ill-defined, soft, asymptom-
atic skin-colored to tan papules or nodules 1. Schwannoma:
ranging in size from 0.2–2.0 cm • Encapsulated
• Plexiform neurofibromas are most com- • Antoni A and Antoni B areas
monly seen in the limbs, where they may • Verocay bodies
be seen as huge pendulous masses caus- • Sclerotic vessels
ing deformity, which in extreme cases are 2. Palisaded and encapsulate neuroma:
known as elephantiasis neurofibroma- • Usually in the face
tosa. There is almost always associated • Well-circumscribed lesions with clefts inside
the neoplasm Schwannoma
osseous hypertrophy in the bony struc-
tures underneath these masses • No myxoid stroma
Special studies
• Immunohistochemically, the neoplas-
tic cells stain positive with antibodies
against the S-100 protein and Leu-7
• Occasionally neurites are also found within
neurofibromas, which can be demonstrated
using antibodies against neurofilament Palisaded and encapsulated neuroma
• CD34 is sometimes focally positive

• Plexiform neurofibroma carries a higher probability of malignant trans-
Clinical Variants formation (2–13%)
• Neurofibromatosis type 1 and 2

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Schwannoma (neurilemmoma) Epidemiology
• More common in women with onset at
Introduction age 20–50 years
Schwannomas or neurilemmomas are benign encapsulated neoplasms that can • Uncommon disease
affect any anatomical site but are preferentially found in the head, neck and • 90% are solitary lesions
extremities. In contrast to neurofibromas these neoplasms are not associated • Unknown etiology, possible link to NF2
with neurofibromatosis. gene
• Occasionally associated with meningio-
Histological features mas or neurofibromatosis
1. Well-circumscribed nodules, surround- Pathophysiology

ed by a capsule formed by perineurium
2. Two different areas which in some foci 1 • The tumor results from the proliferation
are imperceptibly merged: of Schwann cells of peripheral nerve
a. Antoni A sheath derivation
b. Antoni B • Mutations in the NF2 gene, located at
• Antoni A areas have increased cel- 22q12.2 is characteristic of vestibular
lularity of spindle cells with wavy schwannomas and other tumors; and in
nuclei, slightly granular cytoplasm and (familial) schwannomatosis
indistinctive borders. In some foci the
nuclei have a palisaded arrangement Clinical features
(Verocay bodies), a characteristic fea- • The tumor is gray–white in color, encap-
ture of schwannomas sulated, with a smooth, glistening ap-
• Antoni B areas are less cellular and are 2b
pearance, measuring 2–4 cm in diameter
formed by a myxoid stroma contain- • Cystic change is sometimes present, par-
ing dilated vessels, some of which have ticularly in the larger, deeper tumors
thick, sclerotic walls and Schwann cells • Slow-growing, usually solitary tumors
Histological variants: with a propensity for the limbs of adults
• Cellular schwannoma: well-circum- 2a • Pain, tenderness, and paresthesia may be
scribed, symmetrical, encapsulated present in up to one-third of lesions
neoplasms with increased cellularity
and more atypia than regular schwan- Special studies
nomas, occasional mitotic figures, but • Immunohistochemically schwannomas
behave in a benign fashion stain strongly with the S-100 protein, col-
• Ancient schwannoma: characterized Schwannoma lagen type IV and Leu-7
by cytologic atypia and degenerative • No axons can be demonstrated in these
changes including cystic areas, calcifications, hemorrhage with thromboses, lesions
thick vessels with sclerotic walls, xanthomatous areas, fibrosis, siderophages
and atypical cells with bizarre, pleomorphic nuclei
• Plexiform schwannoma: lesion formed by multiple, well-delimited nodules,
separated by fibrous tissue
• Most of these nodules are composed of Antoni A areas with a variable
number of Verocay bodies. Antoni B areas are fewer or absent. Plexiform
schwannomas are not associated with either malignant transformation or
with von Recklinhausen’s disease
• Psammomatous melanocytic schwannoma (PMS): associated with Carney’s
syndrome and can be multiple. It is well circumscribed and is less likely encap-
sulated than classic schwannoma. It shows heavily pigmented dendritic melano-
cytes. The melanin is produced by the neoplastic cells. Psammoma bodies are
found in varying number. Occasionally they can metastasize causing death of
the patients
Important Things To Know Clinical Variants

• Solitary, plexiform schwannomas
• Recurrence and malignant transformation are exceedingly rare
• Psammomatous melanocytic schwanno-
ma (associated with Carney’s syndrome)
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1. Palisaded and encapsulated neuroma:
• Well-circumscribed neoplasm
• No capsule
• Usually located on the face
• No Verocay bodies
2. Angioleiomyoma:
• Smooth muscle cells with blunt-ended nuclei and more eosinophilic cyto-
plasm
Palisaded and encapsulated Angioleiomyoma

neuroma
Schwannoma variants
Cellular schwannoma Cellular schwannoma
Ancient schwannoma Plexiform schwannoma
Psammomatous melanocytic schwannoma

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Perineurioma Epidemiology
• Cutaneous perineurioma is relatively
Introduction common
Perineurioma is a rare benign neural neoplasm, composed exclusively of peri- • Found mainly on the lower limbs of
neurial cells. It was originally described as presenting in the subcutaneous tissue middle-aged adults
as soft tissue perineurioma or storiform perineural fibroma. • Predilection for females
Histological features Pathophysiology

1. Well-circumscribed tumor • Unknown
2. Bland, short, spindle-shaped cells arranged in fascicles, with a focal whorling
and a storiform pattern Clinical features
Other features: • Presents as a small papular lesion, mainly
• Tumor cells may have epithelioid morphology on the lower limbs of middle-aged adults
• Variable hyalinization of the collagen is present and some cases show scat-
tered, mononuclear inflammatory cells Special studies
• Histological variants: intraneural, sclerosing, soft tissue, malignant • Tumor cells are diffusely positive for
EMA, claudin, and Glut-1, but negative
for other neural markers (including S-100
protein), in keeping with perineurial dif-
1 ferentiation
2
Perineurioma
1. Acquired digital fibrokeratoma:
• Admixture of prominent fibroblasts and vessels
• Negative for EMA
2. Neuroma:
• Lack a storiform pattern
• Generally S-100 protein positive
3. Infantile digital fibroma:
• Proliferation of fibroblasts with characteristic cytoplasmic inclusions
• Inclusions positive for vimentin and phosphotungstin hematoxylin Acquired digital fibrokeratoma
Infantile digital fibroma

Neuroma Infantile digital fibroma

• Soft tissue perineurioma has very similar clinical features to those of
cutaneous variants but lesions are subcutaneous and tend to be larger
(up to 5 cm)
• Behavior is benign with no tendency for local recurrence
• Malignant soft tissue perineuriomas are exceptional Clinical Variants
• None
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Epidemiology Palisaded and encapsulated
• Affects equally both males and females
and it is more common in adults
neuromas
Pathophysiology Introduction
Palisaded and encapsulated neuromas (PENs) clinically presents as solitary,
• Some of these cases occur predomi-
small hemispheric papules color skin and usually localized to the face.
nantly on the face and are associated
with acne-like changes, suggesting that
minor trauma may play a role in their
histogenesis 1. Well-circumscribed lesion made up of fascicles of nerve fibers and Schwann
cells
Clinical features 2. Small clefts separating the fascicles of neoplastic cells and the surrounding
stroma (a characteristic finding)
• Solitary well-circumscribed papules
3. Appearance of the encapsulation due to a compression of the perilesional col-
usually on the face, but they can also
lagen fibers due to the expansile growth of the neoplasm
be seen in the buccal, nasal, or genital
mucosa Other features:
• These lesions are most of time confused • In some cases, the nuclei of the neoplastic cells showed a palisaded array
with melanocytic nevi or basal cell • Histopathological variants of PEN, include plexiform and epithelioid variants
carcinomas
Special studies
• Positive for S-100
• Variable number of axons, which stain
positive for neurofilament protein 1 3
Palisaded and encapsulated neuroma
1. Neurofibroma:
• Not as circumscribed as PEN
• No clefts inside the tumor
2. Schwannoma:
• Well-circumscribed lesion surrounded by perineurium
• Verocay bodies
• EMA positivity at the periphery of the lesion
Neurofibroma
Schwannoma

Clinical Variants • Occasionally PEN may present with multiple lesions
• None
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Cutaneous ganglioneuroma Epidemiology
• Affects both males and females
Introduction • No age preference
Cutaneous ganglioneuroma is a rare entity with only a few cases described so • More common in the trunk and rarely
far. affects the face and limbs
Histological features Pathophysiology

1. Ganglion cells, which are large with a round to star shape, prominent ve- • This lesion is a hamartoma and results
siculous nuclei, and cytoplasm filled with granules (Nissl substance) from abnormal migration of ganglion
2. Randomly distributed fusiform cells, embedded in a myxoid matrix and Schwann cell precursors, which are
derived from the neural crest to the skin
Other features:
• Nerve fibers may be found in the deeper parts of the lesion Clinical features
• Clinically, these lesions appear as pap-
2 ules, nodules or pedunculated lesions
Special studies
1 • Ganglion cells stain with neurofilament,
neuron-specific enolase, synaptophysin
and glial fibrillary acidic protein, but do
not stain with S-100 while the fusiform
cells are intensely positive for this marker
Cutaneous ganglioneuroma Cutaneous ganglioneuroma
1. Cutaneous metastasis of neuroblastoma:
• Clinical data is helpful
Neuroblastoma

• Rare entity with only a few cases described to date
Clinical Variants
• None
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Nasal glioma
Introduction
Nasal gliomas (NGs) are rare, slowly growing choristomas that are detected early
in infancy or childhood, and are localized to the nasofrontal region. They are
composed of glial tissue with occasional neurons
1. Ill-defined neoplasm of variable size that involve the dermis and subcutane-
ous tissue
2. Groups of astrocytes with pale, fibrillary and/or granular cytoplasm and a
centrally placed nucleus
Epidemiology 3. No pleomorphism and no mitotic figures are noticeable
4. The collections of astrocytes are separated from one another by variable
• May be present at birth or develop dur- amounts of collagen
ing the first months of life
• No gender predilection Other features:
• Sometimes there are prominent multinucleated cells, associated with abun-
Pathophysiology dant pale cytoplasm
• No typical neurons are usually identified, but a prominent neuronal compo-
• Nasal gliomas may be considered small nent has been described
encephaloceles caused by trapping of • Encephaloceles, which are rare, congenital, cystic malformations, may be con-
glial tissue within subcutaneous tissue sidered to be the cystic variant of NG. The cavity of the cyst is usually filled
during early embryonic development with cerebrospinal fluid and blood, and is lined by a thin layer of ependymal
cells. The wall of the cyst is formed by glial tissue and skin. The glial tissue is
Clinical features histologically similar to that seen in nasal gliomas. Encephaloceles are con-
• NGs are situated either at the root of nected usually to the brain and cerebral ventricles by a stalk of glial tissue that
the nose or intranasally, or in both sites extends through a defect in the cranium
concurrently
• When the latter occurs, communication
exits between the intranasal and extrana- 1 2,3
4
sal parts usually through a defect in the
middle of the nasal bone or at its lateral
margin
• 20% of nasal gliomas are connected to
the brain by a pedicle of glial tissue. For
this reason, before manipulating a nasal
glioma it is important to establish that
there is no connection with the brain, to Nasal glioma Nasal gliomas
avoid complications such as infections
or cerebrospinal liquid leakage. In most
cases they are single lesions, with mul- Histological differential
tiple neoplasms being found only rarely 1. Meningothelial hamartoma:
• Small collections of meningothelial cells
Special studies • Pseudovascular spaces
• Strongly positive for vimentin, S-100 • No psammoma bodies
protein, CD57, and glial fibrillary acidic
protein
Meningothelial hamartoma

• In some cases there are communications with the frontal lobe, this com-
Clinical Variants munication must be interrupted before excision of the skin lesion
• Encephaloceles
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Cutaneous meningioma Epidemiology
• Most commonly seen in children and
Introduction young adults, but may appear at any age
Meningiomas, are among the most common neoplasms in the central nervous • Usually on the scalp, face, or in the para-
system, and are characterized by their sharp circumscription and benign spinal region
behavior. These neoplasms are rarely found in locations other than the central • They may present either as solitary or
nervous system and when they are, it is usually in the orbit or the skin. There multiple neoplasms
are three types of meningiomas: type I or congenital meningiomas; type II me-
ningiomas are localized near sensory organs; and type III meningiomas that Pathophysiology
are extensions from the central nervous system. • Congenital meningiomas result from
failure in the closure of the neural tube
Histological features during embryonic development
1. Symmetrical and well-circumscribed benign neoplasms involving dermis • Meningiomas localized to near sensory
and sometimes extending into subcutaneous tissue organs results of remnants of arachnoidal
2. Nests and clusters of cells arranged in whorls. Cells are in a syncytial arrangement tissue entrapped in the neural sheaths of
cranial or spinal nerves
Other features: • Type III meningiomas are extensions
• The epidermis is spared of meningiomas that originated in the
• Laminated formations with or without calcification (psammoma bodies) central nervous system
• An uncommon type of cutaneous meningiomas is the so-called angioblastic
meningioma or meningothelial hamartoma. This neoplasm is typified by Clinical features
prominent pseudovascular spaces, which cause it to resemble a vascular
neoplasm • These neoplasms may be either firm or
• The three types of meningiomas are very similar to one another histopato- soft, and may have digitated projections
logically, although type II and III meningiomas are associated with a vari- • There are differences between three
able number of inflammatory cells, whereas the congenital type of menin- types of meningiomas:
gioma (type I) is devoid of inflammatory cells o Type I represents congenital meningio-
mas result in the presence of ectopic
meningeal tissue in the dermis and
subcutaneous fat. This variant has
good prognosis and most commonly
2
occurs on the scalp, forehead, and
paravertebral region
1 o Type II comprises meningiomas local-
ized to near sensory organs, such as
the eye and ear, and involve the skin
by continuity. Type II meningiomas
Cutaneous meningioma produce symptoms that depend upon
the sensory organ involved (e.g.
Histological differential proptosis and periorbital edema when
positioned near an eye, or tympano-
1. Cellular neurothekeoma: mastoiditis when situated within or
• Irregular collections of epithelioid cells near the temporal bone)
which anastomose with each other o Type III meningiomas involve the skin
• Lobular pattern of growth through surgical defects, erosion of the
• S-100 negative, positive for NK1-C3 cranial vault or metastasis to the skin
(CD63)
• Cells with abundant amphophilic cyto- Special studies
plasm with ill-defined cell borders
• Usually positive for vimentin and EMA,
Cellular neurothekeoma D2-40/podoplanin
• Positivity for S-100 is variable
• It must be emphasized that cutaneous meningiomas are sometimes
directly connected to the central nervous system. Extreme caution
needs to be taken, in their manipulation because complications such as
meningitis may result
Clinical Variants
• None
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Epidemiology Granular cell tumor
• Most commonly in the skin and tongue
• In most cases they are single entities Introduction
• Mainly affect people in the third to the Granular cell tumors (GCT) are a group of neoplasms named for their distinctive
fifth decade of life appearance under the light microscope. They are characterized by the presence
• More common in women than in men of cells with large, granular and eosinophilic cytoplasm. GCT is an asymptom-
atic, slow-growing neoplasm and is usually an incidental finding. Most authors
Pathophysiology agree that GCT, especially those localized in the mouth and the skin, have
• Immunohistochemical and ultrastructural neural differentiation.
studies have demonstrated the schwann-
ian lineage of tumor cells in granular cell Histological features
tumor 1. Small, poorly circumscribed neoplasm present in the dermis and occasionally
in the subcutaneous tissue
Clinical features 2. Pseudoepitheliomatous hyperplasia
• They present as small, firm masses, 3. Nests or strands of pale-staining, round to polygonal cells with a centrally
either sessile or pedunculated, with ill- placed, small nucleus and faintly eosinophilic cytoplasmic granules
defined margins 4. The stroma composed of connective tissue
• The color varies from pink to greyish Other features:
brown • Older lesions may show prominent desmoplasia with few granular cells
• The overlying epidermis may be hyper-
keratotic or verrucous and is sometimes
ulcerated which may lead to their being 2
confused with malignant neoplasms 3
Special studies 1
4
• Positive staining with the S-100 protein

• PAS is positive
Granular cell tumor
Granular cell tumor
1. Dermatofibroma:
• Proliferation of fibroblasts admixed with kelloi-
dal collagen
• Presence of multinucleated cells occasionally
• S-100 negative and Factor XIII positive
2. Leiomyoma:
• Proliferation of fascicles of smooth muscle cells
intersecting with each other
• Actin, desmin positive, S-100 negative
Dermatofibroma

• In superficial biopsies, GCT can be
confused with squamous cell carcinoma
because of the degree of epidermal hy-
perplasia
Clinical Variants
Leiomyoma
• None
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VASCULAR TUMORS
Hyperplasias • Pyogenic granuloma
Introduction
Pyogenic granuloma (PG) is a hyperplastic process. The lesion grows rapidly
at sites of superficial trauma. In some cases lesions of PG are associated to
endocrine alterations or medication and usually involute upon cessation of the
stimuli.
1. Fully developed lesions of PG are polypoid and show a lobular pattern with
fibrous septa intersecting the lesion Epidemiology
2. Each lobule is composed of aggregations of capillaries and venules lined by
plump endothelial cells • Can develop at any age, but is more com-
3. Pale edematous stroma mon in children and young adults
Other features: Pathophysiology

• Early lesions of PG are identical to granulation tissue, to wit, numerous
capillaries and venules disposed radially to the skin surface, which is often • Majority of the cases have no apparent
eroded and covered with scabs cause, a minority follow trauma or reti-
noid therapy
• Hormonal factors may be involved in
their genesis
Clinical features
3
• Affects both the skin and mucous mem-
1,2 branes
1,2
• Rapidly growing solitary red friable pap-
ule or nodule
• May develop following minor trauma
Pyogenic granuloma Pyogenic granuloma • Occurs most often on an exposed surface
Histological differential Special studies

1. Hemangioma: • The vascular markers CD31, CD34 and
• No edema and prominent septa factor VIII are positive
• No inflammation
2. Bacillary angiomatosis:
• More neutrophils
• Purple cytoplasmic inclusions in endothelial cells which represent bacilli
Hemangioma Bacillary angiomatosis
Clinical Variants
• Cutaneous
• Intravascular PG appears as a PG inside of a vein • Mucosal
• Solitary
• Multicentric
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Benign Neoplasms
Infantile hemangiomas
Introduction
Infantile hemangioma is the most common benign vascular proliferation, and
traditionally has been considered a neoplasm. The majority of these lesions, after
an initial proliferative phase, undergo complete regression through a process of
Epidemiology fibrosis, even in the absence of therapy. True neoplastic infantile hemangiomas
• The most common tumors of infancy, include noninvoluting congenital hemangiomas (NICH) and rapidly involuting
with an incidence in the newborn popu- congenital nonhemangiomas (RICH). These two lesions do not regress as do the
lation of approximately 2% other infantile hemangiomas
• There is a female preponderance
Pathophysiology 1. Early hemangiomas are highly cellular and are characterized by plump endo-
• A locus for autosomal dominant pre- thelial cells aligned to vascular spaces with small inconspicuous lumina
disposition to hemangiomas has been • The histopathological composition of infantile hemangiomas varies with the
identified on chromosome 5q age of the lesion
• Ischemic placental injuries are associated • As the lesions mature, blood flow increases, endothelium flattens, and the
with an increase in infantile hemangio- lumina of the vessels enlarge and become more obvious
mas • During this interval the vessels convey a “cavernous” appearance that can be
misinterpreted as a venous malformation. Regression is portrayed as progres-
Clinical features sive interstitial fibrosis and adipose metaplasia, a process without known
stimulus
• Infantile hemangioma is the most com-
mon tumor of infancy. It is usually not
present at birth but becomes apparent 1
within first few weeks of life and is more 1
common in premature infants. The
majority of lesions regress by 5-7 years
of age
• Usually bright red to blue papule, nodule,
or plaque varying in size from a few mil-
limeters to several centimeters Infantile hemangioma

• GLUT-1+, WT1+, CD31+ are positive in 1. Pyogenic granuloma (PG):
classical infantile hemangiomas • PG is often ulcerated and has edema and inflammation
• GUT-1 is negative in NICH and RICH
Pyogenic granuloma
Clinical Variants Important Things To Know

• Rapidly involuting congenital heman- • Glut-1 allows discrimination between classical infantile hemangiomas,
gioma (RICH) RICH, and NICH
• Non-involuting congenital hemangioma
(NICH)
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Cherry angiomas
Introduction
Senile or cherry angiomas, known also as Campbell de Morgan spots are
among the most frequently acquired cutaneous vascular lesions.

1. Cherry angioma consists of dilated capillary blood vessels localized in the • They appear early in adulthood, most
superficial dermis commonly on the trunk and lower
2. The vessels have variably thickened walls extremities with time, may increase in
3. Fully developed lesions are associated with a loss of the rete ridges of the number and size
epidermis that leads to the formation of a peripheral collarette of adnexal epi-
thelium, thus creating a polypoid lesion Pathophysiology
Other features: • Some authors have suggested that cherry
• Mast cells may be numerous, while the endothelial cells that line the vessels angiomas may be related to a recent rise
express a strong carbonic anhydrase activity, as a correlate with the fenestra- in the atmospheric temperature, since the
tion of the venous capillaries number of lesions per patient increased
and decreased proportionate to the tem-
perature
• Eruptive cherry hemangiomas have also
3 1 2
been concurrent with ECHO viral infec-
tions, as well as exposures to chemical
compounds, notably glycol ether solvent
2-butoxyethanol, sulfur mustard gas, and
bromides
Cherry hemangioma
Clinical features
Histological differential • They appear early in adulthood, most
commonly on the trunk and proximal
1. Angiosarcoma: limbs and with time, may increase in
• Poor circumscription number and size. On presentation they
• Irregular vascular spaces which anastomose with each other are small red papules that resist compres-
• Atypical endothelial cells sion
Special studies
• Proliferation activity is very low, as
expressed negatively by an absence of
immunohistochemical reactivity for Ki67
• CD31 and CD34 positivity in the endo-
thelial cells
Angiosarcoma

• Hormonal factors have also been suspect. It has been observed that
pregnant women are disposed during pregnancy with lesions that invo-
lutes post-partum
Clinical Variants
• None
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Arteriovenous hemangioma
Introduction
This lesion was first named cirsoid aneurysm, because of the presence of a
spiraled blood vessel (feeder vessel) extending from the subcutaneous fat into
the lesion. Recently, it was renamed arteriovenous hemangioma or acral arte-
Epidemiology riovenous tumor. The latter name is not totally appropriate, because this lesion
• Arteriovenous hemangioma is a neo- affects different areas of the body and not only acral skin.
plasm that occurs in mid-adult life
Pathophysiology 1. Well-circumscribed proliferation of thick-walled muscle-containing blood
• The precise nature of acral arteriovenous vessels, lined by a single layer of endothelial cells involving the upper and
hemangioma is uncertain mid-reticular dermis
• Some of studies proposed that it is a 2. There are also thin-walled dilated blood vessels
multicentric hamartoma of the subpapil- 3. Spiraled ascending small muscular artery (“feeder” vessel)
lary vascular plexus with one or more Other features:
arteriovenous anastomosis • The thick-walled blood vessels resemble arteries, but a well-formed elastic
internal membrane is absent. Therefore, they are probably ectatic veins
Clinical features • Arteriovenous shunts
• It presents as a blue to red papule mea-
suring 0.5–1.0 cm, mainly affecting facial
skin
• Larger lesions as well as intraoral and 1
vulvar examples have been also de- 2
scribed
• Usually the lesions are solitary, although
multiple examples have been cited
• When the lesions are multiple they tend
to cluster together
• Occasionally, they are associated with
other abnormalities including epidermal
nevus syndrome, vascular hamartomas 3
and malformations; and several examples Arteriovenous hemangioma
of multiple arteriovenous hemangiomas
have been described in patients with
chronic liver disease
Special studies 1. Glomangioma:
• None • Large dilated blood vessels surrounded by several layer of cuboidal cells
Glomangioma Glomangioma
Clinical Variants
• None
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Microvenular hemangioma
Introduction
Microvenular hemangioma is a recently described benign vascular neoplasm.
1. Poorly circumscribed proliferation of irregularly branched, round to oval,
Epidemiology
thin-walled blood vessels lined by a single layer of endothelial cells, involv- • Affects males and females equally
ing the entire reticular dermis
2. The lumina of the neoplastic blood vessels are inconspicuous and often col- Pathophysiology
lapse with only a few erythrocytes within them • In some patients, a histogenetic relation-
3. Variable degree of dermal sclerosis in the stroma ship between microvenular hemangioma
and hormonal factors, such as pregnancy
and hormonal contraceptives, has been
postulated, but this feature has not been
1
corroborated by other authors
3
2
Clinical features
• Microvenular hemangioma is an ac-
quired, slowly growing asymptomatic
Microvenular hemangioma
lesion with angiomatous appearance
• It is usually solitary, varying in size from
Histological differential 0.5–2 cm
• It most commonly affects the upper
1. Kaposi sarcoma, patch stage: limbs, particularly the forearms. How-
• Irregular anastomosing vascular spaces ever, lesions on the trunk, face and lower
• Newly formed ectatic vascular channels surrounding pre-existing normal limbs have also been recorded
blood vessels and adnexa (promontory sign) • Hemangiomas identical to microvenular
• Plasma cells hemangioma can be seen in patients with
• Hyaline (eosinophilic) globules POEMS syndrome
• Small interstitial fascicles of spindle cells
Special studies
• Immunohistochemically, the cells lining
the lumina show positivity for factor VIII-
related antigen, CD31 and CD34 which
qualifies them as endothelial cells
• Some smooth muscle actin-positive
perithelial cells have been also described
surrounding this vascular space
Kaposi sarcoma, patch stage

• Lesions of microvenular hemangioma are cured by simple excision
Clinical Variants
• None
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Tufted angioma
Introduction
Tufted angioma is an unusual, acquired vascular neoplasm.
1. Multiple individual vascular lobules within the middle and lower dermis and
subcutaneous fat
2. Aggregation of endothelial cells that whorl concentrically around a pre-exist-
ing vascular plexus in each lobule
3. The “cannon ball” pattern is characteristic of tufted angioma
Other features:
Epidemiology • Some lobules bulge into the walls of dilated thin-walled vascular structures,
giving these vessels a slit-like or semilunar appearance
• Most commonly affect children and • Small capillary lumina are identified within the aggregations of endothelial
young adults, but both congenital and cells
very late onset cases have been de-
scribed
Pathophysiology
• Most cases are sporadic, although a
family with several members affected
by tufted angioma has been reported.
In this particular family the mode of
transmission was in an autosomal
1
dominant fashion
Tufted angioma
2,3
Tufted angioma
Clinical Variants
• None
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1. Kaposi sarcoma: • The lesions have a predilection for the
• Nodular lesions of Kaposi sarcoma are composed of interlacing fascicles of neck, upper chest, back, and shoulders,
spindle cells lining slit-like vessels although examples of tufted angioma
• An inflammatory infiltrate of plasma cells is usually present have also been reported on the head,
2. Infantile hemangiomas: extremities and oral mucosa
• Tufted angiomas are rare in infants • Tufted angioma grows slowly and in-
• Occasionally present with a lobular pattern, but these collections are present sidiously, and may eventually come to
only focally cover a large area of the trunk or neck.
In most cases the growth is halted after
some years, but there is a slight tendency
toward spontaneous regression
• The clinical appearance of the lesions is
variable. Some of them are characterized
by enlarging erythematous or brown
macules or plaques with an angiomatous
appearance; other lesions may resemble
granulomas or a connective tissue
abnormality. In some cases the lesions
are tender, while in other cases there
is hyperhidrosis on the surface. Raised
papules resembling pyogenic granulomas
Kaposi sarcoma are sometimes seen within the area of the
lesion and occasionally the lesions may
show a linear arrangement
• Tufted angiomas have been associated
with nevus flammeus and other vascular
malformations, pregnancy, and with non-
regressing lipodystrophy centrifugalis
abdominalis. In some cases the lesion
spread by infiltration, leading to scleros-
ing plaques. Many cases of Kasabach-
Merritt syndrome are associated with
tufted angioma
Infantile hemangioma
Special studies
• The cells in the capillary tufts are weakly
positive or negative for factor VIII-related
antigen
• They exhibit strong positivity for Ulex
europaeus I lectin, EN4, CD31, CD34
and alpha-smooth muscle actin which
is related to the immature nature of the
endothelial cells. The cells that show
reactivity for smooth muscle actin, most
likely represent pericytes
• Tufted angioma showing spontaneous regression is a rare event. For the
treatment of these lesions, soft radiation has been recommended. Sat-
isfactory results have been also reported with surgery, pulse-dye laser,
high-dose of systemic steroids, and interferon-α
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Glomeruloid hemangioma
Introduction
Glomeruloid hemangioma is a vascular proliferation that only occurs in patients
affected with the POEMS syndrome. POEMS is an acronym for this syndrome
which includes: Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal
Epidemiology gammopathy (M protein), and Skin lesions. Histopathologically, the vascular
• No sex predilection lesion in patients with POEMS syndrome fall into four categories: microvenular
hemangiomas; cherry hemangiomas; multinucleate cell angiohistiocytomas; and
Pathophysiology glomeruloid hemangiomas. Glomeruloid hemangiomas seem to be fairly specific
for POEMS syndrome.
• Speculation remains as to the histogen-
esis of glomeruloid hemangioma. There Histological features
is a hypothesis that the deposition of
immunoglobulins within the endothelial 1. Multiple ectatic vascular structures containing aggregates of capillary loops
cells stimulate the proliferation of these resembling renal glomeruli
cells in a glomeruloid fashion 2. The capillaries are lined with either flat or plump endothelial cells with vacu-
oles and surrounded by pericytes
Clinical features
• Glomeruloid angiomas are small, firm,
red to violaceous, dome-shaped papules 2
that measure a few millimeters in diam-
eter and are usually located on the trunk
and proximal parts of the extremities
1
• In some cases the angiomatous lesions
resemble eruptive histiocytomas
Special studies Glomeruloid hemangioma Glomeruloid hemangioma

• The vacuoles in the cytoplasm of the
endothelial cells contain eosinophilic PAS
positive globules that represent deposits Histological differential
of immunoglobulins absorbed through 1. Tufted angioma:
circulation • Composed of solid aggregates of endothelial cells forming lobules, indenting
• The neoplastic cells are positive for factor dilated vessels
VIII-related antigen, Ulex europaeus I • Lack of glomeruloid arrangement
lectin and vimentin • No evidence of eosinophilic PAS positive deposits within the endothelial cells
• Muscle-specific actin is negative
• Two different types of endothelial cells
have been described in glomeruloid hem-
angioma. The first type consists of en-
dothelial cells with large vesicular nuclei
with open chromatin and large amounts
of cytoplasm. These cells are positive for
CD31, CD34, and Ulex europaeus I lectin,
but not for CD68. The second type of en-
dothelial cells consists of cells with small
nuclei containing a dense chromatin Tufted angioma
and scant cytoplasm. This second type
of cells express positively for CD31 and
CD68, whereas CD34 and Ulex europaeus
I lectin are negative

• Most patients with POEMS syndrome have a progressive, disabling
Clinical Variants clinical course with a poor prognosis, in spite of any therapy
• None
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Acquired elastotic hemangioma
Introduction
Acquired elastotic hemangioma is a recently described variant of cutaneous
hemangioma. These lesions develop during adulthood on chronic sun-dam-
aged skin, on the extensor surface of the forearms or the lateral aspects of the
neck. Epidemiology
Histological features • It mainly affects middle-aged and elderly
women
1. Band-like proliferation of capillaries involving only the superficial dermis
2. A narrow band of non-involved papillary dermis separates the newly Pathophysiology
formed capillaries from the normal or flattened epidermis • Sun exposure appears to be an important
3. The neoformed capillaries show small cleft-like or round lumina and con- factor in the development of these lesions
tain few erythrocytes
4. Solar elastosis in connective tissue surrounding or intermingled with the
newly formed capillaries
Clinical features
• Acquired elastotic hemangioma presents
Other features: as a slightly elevated, irregularly shaped,
• No cellular atypia, no hemosiderin deposits or extravasated erythrocytes solitary lesion with violaceous coloration
• The lesions are usually well-demarcated
plaques that range from 2–5 cm in diam-
3 eter
1 4 • The lesions blanch under diascope pres-
sure
2
Special studies
• The neoplastic endothelial cells are
strongly positive for CD31 and CD34
Acquired elastotic hemangioma Acquired elastotic hemangioma • A continuous rim of alpha-smooth
muscle actin-positive pericytes surrounds
the majority of the neoplastic vascular
Histological differential channels
• Proliferating markers Ki-67 and MPM-2
1. Angiosarcoma: stain only a few of the nuclei of the en-
• Usually is located in head and neck, not arms dothelial cells of the newly formed blood
• Irregular proliferation of vessels, not capillaries vessels
• Atypical endothelial cells throughout the dermis
Angiosarcoma

• Treatment consisted of local surgical excision in all cases
Clinical Variants
• None
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Epidemiology Kaposiform
• Most commonly affects children
hemangioendothelioma
Pathophysiology Introduction
• When the neoplasm is positioned in deep
Kaposiform hemangioendothelioma is a rare vascular neoplasm. Though the
soft tissue, mediastinum, or retroperi-
retroperitoneum is the most frequent location, it may also be found in the skin.
toneum, it may be associated with the
consumption coagulopathy that charac-
terizes Kasabach-Merritt syndrome
• In some cases, kaposiform hemangio- 1. Several ill-circumscribed nodules separated by connective tissue
endothelioma may be associated with 2. Admixture of small round capillaries and solid glomeruloid nests containing
lymphangiomatosis round to oval endothelial cells with epithelioid features in nodules
Clinical features Other features:

• The endothelial cells may contain hemosiderin, hyaline globules, and vacuoles
• Affects the skin and also the retroperi- • Short fascicles of spindle cells within nodules
toneum. Some patients may develop the • Absence of atypia and mitotic figures
Kasabach-Merritt syndrome
Special studies
• Immunohistochemical studies have 1
2
provided dissimilar results. In some 1
cases the neoplastic cells were positive
for vimentin, FLI-1, D2-40, CD31 and
CD34 and negative for actin. In the
better-formed vascular channels of the
neoplasm, the latter marker highlights
Kaposiform hemangioendothelioma
pericytes that form a ring around the
negative stained endothelial cells. GLUT1
antibody is negative, but the vascular
endothelial growth factor receptor-3
(VEGFR-3) has been reported positive in 1. Tufted angioma:
six cases studied, which suggests at least • Nodules are smaller and more circumscribed
partial lymphatic endothelial differentia- • Does not involve deep soft tissue or bone
tion of the neoplastic cells in kaposiform 2. Kaposi sarcoma:
hemangioendothelioma. So far, no evi- • Absence of multinodular pattern
dence of human herpes virus 8 (HHV-8) • Infiltrates of plasma cells present around the nodules
infection has been detected in lesions of
kaposiform hemangioendothelioma
Tufted angioma Kaposi sarcoma

• Kaposiform hemangioendothelioma combines features of cellular infan-
tile hemangioma and Kaposi sarcoma
• Kasabach-Merritt syndrome is a major complication of these lesions
Clinical Variants
• None
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Glomus tumor and glomangioma Epidemiology
• Glomus tumor is more common in young
Introduction adults
Glomus tumors are uncommon neoplasms that arise from modified smooth • Glomangioma is more common in in-
muscle cells normally present in specialized arteriovenous shunts in acral sites, fancy and childhood
mainly the fingertips.
Pathophysiology
Histological features • Substance Present in nerve fibers has
Glomus tumor: been incriminated in the pathophysiolo-
1. Well-circumscribed dermal tumor surrounded by compressed fibrous tissue gy of glomus tumors. This substance, it is
2. The neoplasm is cytologically formed of clusters of round or polygonal known to be a primary sensory afferent
monomorphous glomus cells with large round, plump nuclei and scant neurotransmitter for mediating painful
eosinophilic cytoplasm stimuli
• Multiple familial glomus tumors appear
to have autosomal dominant pattern of
inheritance
2
1
Clinical features
• The solitary glomus tumor is more com-
mon. It creates a small, purple nodule
preferentially in acral areas of the
extremities, especially nail beds of the
Glomus tumor fingers
Glomangioma: • There is a striking predominance among
1. Less well-circumscribed lesions than solitary glomus tumors female patients
2. These are composed of irregular dilated endothelial lined vascular channels • Frequently, the lesion creates severe
that contain red blood cells and, distinctively have small intramural aggrega- paroxysmal pain, usually precipitated by
tions of glomus cells exposure to cold or minor pressure
• Some are made up of several nodules within the dermis • In contrast to the solitary glomus lesion,
• Some have an appearance that calls to mind a hemangioma glomangiomas present during childhood
as small bluish nodules situated deep in
the dermis and widely scattered in the
skin
1
Special studies
2
• SMA+, H-caldesmon+, Desmin, CD34,
Glomangioma S-100 are negative
Glomangioma
1. Solid form of hidradenoma:
• Vascularity of glomus and lack of ductal
differentiation help to differentiate
2. Venous malformation:
• Lack of glomus cells
Solid form of hidradenoma Venous malformation

• The tumor is positive for smooth muscle actin (SMA) and vimentin
Clinical Variants
• Cutaneous
• Visceral
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Malignant Tumors
Epidemiology Kaposi sarcoma
• Classic Kaposi sarcoma affects elderly
patients most frequently in males. A Introduction
racial predisposition is recorded, with an Vascular neoplasm caused by human herpes virus 8 (HHV-8).
increased incidence in Ashkenazi Jews
and individuals of Mediterranean de-
scent. It follows a chronic course and the
lesions predominantly involve the lower 1. Plaque lesions involve the entire dermis and even the upper part of the subcu-
parts of the legs taneous fat
• The African-endemic variant of Kaposi 2. At this stage, there is an increased number of spindle cells arranged in short
sarcoma occurs mainly in equatorial Af- fascicles between collagen bundles centered around proliferating vascular
rica. This variant of Kaposi sarcoma has channels
been subdivided into two groups: 3. The spindle cells line irregularly shaped, slit-like vascular spaces that contain
o a benign nodular disease, affecting isolated erythrocytes
mainly young adults Other features:
o a fulminant lymphadenopathic form. • The neoplastic vessels of Kaposi sarcoma show a tendency to be present
This latter form is fatal, it predomi- around pre-existing normal adnexae and blood vessels producing the so-
nantly affects children and kills most called “promontory sign”
of the patients within two to three • At scanning magnification patch stage lesions show sparse, superficial and
years deep perivascular mononuclear cell infiltrates in conjunction with an in-
• The iatrogenic, immunosuppressive, creased number of irregular, jagged, vascular spaces lined by thin endothelial
drug-associated form of Kaposi sarcoma cells
is especially frequent in renal trans- • The vessels are mainly found in the upper part of the dermis
plant recipients, although it has also • In the tumoral stage, the spindle cells are arranged in interwoven fascicles
been reported in other organ transplant with erythrocytes scattered in the interstices
recipients, as well as in a wide spectrum • Plasma cells are present at all stages of the disease
of patients receiving immunosuppressive • Nuclear atypia, pleomorphism and mitotic figures may be seen, but are usu-
drug therapy for different reasons ally not very prominent
• AIDS-associated Kaposi sarcoma is
especially frequent in homosexual men,
found in 21% of all homosexual men with
AIDS
1 2
Kaposi sarcoma patch Kaposi sarcoma plaque Kaposi sarcoma plaque
Clinical Variants
• Classic
• Endemic Kaposi sarcoma tumor Kaposi sarcoma tumor
• Iatrogenic
• AIDS-associated
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Histological differential Pathophysiology
1. Angiosarcoma: • They are the result of the complex
• Irregular dissecting vascular spaces interplay of HHV-8 with immunologic,
• Atypical endothelial cells with nuclear pleomorphism and mitosis genetic, and environmental factors
• HHV-8 is negative
2. Benign lymphangioendothelioma: Clinical features
• Multiple lesions present in a plate-like arrangement
• There are three stages:
• Negative HHV-8
o patch stage: brown-red macules or
patches
o plaque stage: brown-red and blue-
violet Papules or plaques
o tumor stage: violet nodules
Special studies
• CD34+, CD31+, FLI1+, and HHV-8+
HHV-8 staining
Angiosarcoma
Benign lymphangioendothelioma

• The incidence of AIDS-related Kaposi sarcoma has decreased in the last
few years
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Angiosarcoma
Introduction
Malignant neoplasm of endothelial cells with poor prognosis. There are three
variants: angiosarcoma (AS) of the face and scalp; radiation-induced AS; and AS
associated to chronic lymphedema.
1. Poorly circumscribed dermal tumor
Epidemiology 2. Ectatic dissecting bizarre vessels
3. Atypical endothelial cells with nuclear pleomorphism and mitosis
• Usually affects the face or scalp in elderly
patients, and it is more common in white
people
• It also can affect the areas of chronic 3 2
lymphedema, and chronic radioderma-
titis
1
Pathophysiology
• Arises from vascular endothelium. An al-
teration of the TP53/MDM2 pathway was
documented in cases of angiosarcoma Angiosarcoma Angiosarcoma
Clinical features Histological differential

• Clinically, angiosarcomas of the face ap-
pear as ill-defined bruise-like areas that 1. Kaposi sarcoma:
simulate a hematoma • Spindle cell tumor with plasma cell
• More advanced lesions present as • Positive for HHV-8
indurate plaques with raised, nodular, • Endothelial cells are not atypical
and occasionally ulcerated components 2. Malignant melanoma:
accompanied by smaller satellite lesions • Positive for melanocytic markers such as S-100, HMB-45, Mart-1, and pan-
in the vicinity melanoma
• Epidermal part of melanoma, if present, helps to differentiate
Special studies
• D2-40+, CD31+, CD34+, HHV-8–
Kaposi sarcoma
Malignant melanoma
Clinical Variants
• Idiopathic cutaneous angiosarcoma of
the head and neck
• Lymphangiosarcoma arising in chronic • Regardless of the variant of AS the histological features are similar
lymphadematous limbs
• Postirradiation angiosarcoma
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CUTANEOUS CYSTS
Epidermoid cyst (follicular
infundibular cyst/epidermal
inclusion cyst)
Introduction
Epidermoid cyst is the most common cutaneous cyst. These can occurs anywhere,
but are mostly seen on the face and upper trunk.
Epidemiology
Histological features • Young to middle-aged adults
1. Cystic cavity filled with laminated keratin • Seen on face, neck, upper trunk and
2. Stratified squamous epithelium identical to the epidermis scrotum
Other features:
• Acute/chronic granulomatous inflammation (in case of rupture)
Pathophysiology
• Derive mostly from follicular infun-
dibulum
• May be primary but also can arise from
traumatically implanted epithelium
1 (true epidermal inclusion cysts) or
disrupted follicular structures
• Multiple cysts can occur with Gardner
2 syndrome and nevoid BCC syndrome
• Development of BCC or SCC within
Epidermal cyst the cyst is very rare

Pilar cyst: • Well-demarcated, skin-colored or yel-
• Lack of granular layer lowish dermal nodules
• Compact and homogenous contents (loose and flaky • May have a visible punctum, represent-
in epidermal cysts) ing the opening of the hair follicle from
• Calcification may be present which the cyst arises
• Few millimeters to several centimeters
Dilated pore of Winer: in diameter
• Communication with skin surface • Usually asymptomatic, but with pres-
• Epithelial lining is acanthotic sure may release a creamy odorous
• Plate-like extensions and budding content
Pilar cyst • Rupture is accompanied by pain due to
inflammation
Important Things To Know • Tiny superficial cysts are known as
• In Gardner syndrome, cysts may milia
show columns of shadow cells • Scrotal calcinosis is due to dystrophic
(pilomatricoma-like) projecting into calcification within multiple scrotal
the cyst cavity cysts
• Infection of the cyst epithelium with
HPV can lead to irregular acantho- Special studies
sis, hypergranulosis and sometimes • None
koilocytes in the wall of the cyst
• Excision is curative although cyst Dilated pore of Winer
may recur if the cyst wall is not
completely removed Clinical Variants
• None
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Pilar cyst (trichilemmal cyst)
Introduction
Benign epithelial lined cyst.
Epidemiology 1. Lined by epithelium similar to the isthmic part of the hair follicle which is
• There is strong female preponderance devoid of a granular layer (abrupt keratinization)
2. Peripheral palisading of nuclei
Pathophysiology 3. The cyst contents are made of a compact homogenous keratin
• Pilar cysts arise from the isthmus of 4. Calcification
anagen hairs or from the sac surrounding Other features:
catagen and telogen hairs, areas where • Located in the middle to deep reticular dermis
the inner root sheath is lacking • Absence of intercellular bridges between the keratinocytes
• Proliferating trichilemmal cyst (PTC) • Multinucleated keratinocytes (when ruptured)
or pilar tumor arises from irritation of • PTC consists of large, well-defined lobulated solid and cystic masses of pro-
a pre-existing pilar cyst. It is frequently liferating keratinocytes with trichilemmal type of keratinization. The kerati-
described as a benign neoplasm, but nocytes may exhibit cytological atypia and mitosis may be seen in the basal
potential for malignant transformation layer. Squamous eddies are seen
has been reported • Malignant PTC has infiltrative growth pattern, significant atypia and large
number of mitotic figures
Clinical features
• Pilar cysts occur predominantly on the 1,2
3
scalp of elderly woman
• Usually solitary nodulocystic lesion, but
can be multiple 4
• Size ranges from 1–10 cm in diameter
• Malignant PTC include: non-scalp loca-
tion, size >5 cm and a history of a recent
and rapid increase in size
Special studies Pilar cyst Pilar cysts
• None
1. Epidermal inclusion cyst:
• Lined by epithelium with prominent granular layer
• Stratum corneum laminated
Epidermal inclusion cyst

• Proliferating trichilemmal cyst is considered as a low-grade squamous
cell carcinoma by some authors
Clinical Variants
• None
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Dermoid cyst
Introduction
Dermoid cysts are large lesions located in the dermis or subcutis and appear as
discrete, subcutaneous nodules.

1. Stratified squamous epithelium • Present at birth, along an embryonic fu-
2. Granular layer sion plane
3. Contains mature epidermal appendages connected to the wall • May not be noticed until early childhood
when they get inflamed, enlarged, or
Other features: infected
• Hairs may project into the cyst wall • Rarely, they may go unnoticed until
• Contains other normal structures like hair, eccrine glands, sebaceous lob- adulthood
ules, apocrine glands, or smooth muscle
Pathophysiology
1,2 • Congenital defect
3
Clinical features
• Well defined, rubbery, hard, raised,
Dermoid cyst yellow-to-pink
• Fine hairs on surface may be seen
• 1–4 cm in diameter
• Most frequently seen around the eyes
Histological differential (especially lateral eyebrow) or midline
of face. May be found on neck, sternum,
1. Epidermoid cyst: sacrum, and scrotum
• Lack adnexal structures in wall • May extend into the bone
2. Steatocystoma: • Lesions do not transilluminate
• Wall of the cyst offers a crenulated appearance similar to the sebaceous duct
• Has eosinophilic cuticle on the luminal side of the epithelial lining Special studies
• Has sebaceous gland in cyst wall • None
Epidermoid cyst Steatocystoma

• Since neural heterotopias are included in the differential, imaging may
be appropriate prior to rule out the possibility of connection with the
CNS
Clinical Variants
• None
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Steatocystoma
Introduction
Steatocystomas are dermal cysts that occur as single or multiple lesions (steato-
cystoma simplex versus multiplex) and drain oily fluid if punctured.

• Usually appears at puberty 1. Dermal cyst lined by thin stratified squamous epithelium
2. No granular layer
Pathophysiology 3. Glassy, pink (eosinophilic) crenulated cuticle overlies the internal surface
• Autosomal dominant 4. Small sebaceous lobules in or adjacent to cyst wall
• Mutations in the KRT17 gene
• Possible androgenic influence
• Mechanism unknown:
o retention cysts versus 1,2
o dermoid cyst variant versus
o nevoid or hamartomatous condition of 4
the pilar sebaceous duct zone
4 3
Clinical features
• Few millimeters to centimeters in diam- Steatocystoma Steatocystoma
eter
• Most common on chest, axillae and groin
• Unusual variants include facial, acral, and Histological differential
a rare congenital linear form
• Persist indefinitely, but are asymptomatic 1. Milia:
• Lacks the cuticle
Special studies • Lacks sebaceous glands in wall
2. Trichostasis spinulosa:
• None • Clinically unapparent
• Plugged follicle opens to surface with numerous vellus hairs
• Not a cyst
Trichostasis spinulosa
Clinical Variants
• Steatocystoma simplex
• Steatocystoma multiplex
• Facial • Steatocystoma treated by excision/incision and removal of the cyst wall
• Acral
• Congenital linear form
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Bronchogenic cyst
Introduction
Bronchogenic cyst is the product of sequestered respiratory epithelium during
embryologic development. They are located on the neck and within the tho-
racic cage surrounding the bronchial trees but may be localized to ectopic sites.
Epidemiology
Histological features • Usually present at birth
1. Lined by pseudostratified and ciliated columnar epithelium • Four times more common in males than
2. Smooth muscle and mucous glands, and rarely cartilage, in cyst wall females
Other features:
• Interspersed mucin-filled goblet cells within epithelium
Pathophysiology
• Metaplasia may lead to some areas of stratified squamous lining as well as • Respiratory epithelium is sequestered
ciliated columnar and goblet cells during development of the embryonic
tracheobronchial tree
• Migration of tissue to ectopic sites results
in localization outside the developmental
1 areas of the tracheal bronchial tree
Clinical features
2
• Solitary
• Commonly found in suprasternal notch
• Rarely seen on the anterior neck or chin,
face, back, shoulder, or abdomen
Bronchogenic cyst Bronchogenic cyst • Located in subcutis and may be connect-
ed to epidermis via a fistulous tract
Histological differential • Rarely present as a pedunculated growth
1. Branchial cleft cyst: Special studies

• Presence of Lymphoid follicles • None
2. Cutaneous ciliated cyst:
• Clinical presentation and location
Cutaneous ciliated cyst

• Malignant transformation is very rare
Clinical Variants
• None
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Cutaneous ciliated cyst
Introduction
Cutaneous ciliated cysts are uncommon and typically occur on the lower extrem-
ities of young women. This cyst is also known as cutaneous Müllerian cyst and
cutaneous ciliated cystadenoma.
Epidemiology
• Young women; teen to young adults Histological features
• Rarely seen in men 1. Unilocular or multiloculated
2. Located in subcutis or deep dermis
Pathophysiology 3. Simple cuboidal to columnar ciliated epithelium comprises the cyst wall
• Controversial 4. Papillary projections into the cyst lumen are common
• Müllerian duct origin Other features:
• An alternative hypothesis seeks to ex- • May have areas of squamous metaplasia
plain the few cases in men and holds that
eccrine glands undergo ciliated metapla-
sia
Clinical features 4
• Usually solitary, a few centimeters in 1,2
diameter
• Lower extremities on young females, 3
often on the sole but can be seen on but-
tocks
• Drain clear to amber fluid, if ruptured. Cutaneous ciliated cyst Cutaneous ciliated cyst
Cyst usually appears empty due to rup-
ture during biopsy
Special studies 1. Bronchogenic cyst:
• None • Contains lymphoid tissue in wall
2. Thyroglossal duct cyst:
• Thyroid follicles in cyst wall

• Some suggest both cutaneous ciliated cyst and ciliated cyst of the vulva
should be called cutaneous Müllerian cysts due to the same origin
Clinical Variants
• None
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Median raphe cyst
Introduction
Median raphe cyst (also known as apocrine cystadenoma of the penis) is a rare,
small cyst occurring on the penis in young men.

1. Unilocular, irregularly shaped cystic spaces, not connecting to the overlying • Young men
epithelium
2. Pseudostratified or stratified columnar epithelium, 1-4 cells layers thick Pathophysiology
Other features: • Develop due to aberrant urethral epithe-
• Mucin-containing cells lium
• Cyst may appear empty due to fluid leakage during biopsy • Caused by incomplete closure of ure-
• Ciliated lining is very rare thral or genital folds or by outgrowths of
embryologic epithelium occurring after
primary closure of folds
Clinical features
1 2
• Solitary
• Usually a few millimeters in diameter,
but may extend linearly over several
centimeters
• Midline ventral aspect of the penis, on or
near glans
Median raphe cyst Median raphe cyst • Do not connect to urethra

• None
• Location and nature of lining make diagnosis obvious

• Treat by excision
Clinical Variants
• None
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CUTANEOUS METASTASES
Cutaneous metastases
Introduction
Cutaneous metastasis may be the first indication of a visceral cancer. How-
ever, most metastases develop months or years after the primary malignancy
has been diagnosed. Sometimes, cutaneous metastasis and the primary tumor
are diagnosed simultaneously.

• The incidence range from 1.2–4.4%. One 1. Metastases are centered on the dermis but they can extend into the subcu-
study showed that the most common pri- taneous tissue
mary tumors in women were breast and 2. The epidermis is usually spared, but it can be affected in some cases such
in men were lung as breast carcinoma (Paget’s disease) or carcinomas of the bladder or colon
• Cutaneous metastases are more likely to (extramammary Paget’s disease)
be seen in older individuals. In neonates
they are usually derived from a neuro- Other features:
blastoma or rhabdomyosarcoma • They may resemble the primary tumor.
• More than 60% are adenocarcinomas. However, often it is necessary to perform
About 15% are of squamous cell carcino- special stains in order to determine the
mas. The rest are melanomas, undiffer- primary source of the neoplasm
entiated neoplasms or others 2
Pathophysiology
• The tumor cells may reach the skin by
direct extension, by accidental implanta-
tion during a surgical procedure and by 1
lymphatic and hematogenous spread
Clinical features
• Multiple, discrete, painless, freely mov-
able nodules of sudden onset. They are
usually 1–3 cm in diameter Renal cell carcinoma
• They vary in color from red to bluish
purple to light brown or flesh color
• It tends to occur on the cutaneous sur-
face near to the site of the primary tumor
• Approximately 5% of metastases involve
the scalp
• Metastasis to the umbilicus is also quite
common (Sister Mary Joseph nodule)
Breast carcinoma
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The differential diagnosis depends on the primary source of the neoplasm. To • Breast: CK7, GCDFP15, ER and PR are
cite a few examples: positive. CK20, CK5/6, S-100 &TTF-1 are
• Clear cell hidradenoma: is the main differential diagnosis of renal cell carci- negative
noma • Lung: CK7 and TTF-1 are positive.
• Endometriosis is the differential diagnosis of endometrial carcinoma and CK20,CK5/6, and S-100 are negative
other adenocarcinomas. • Thyroid: thyroglobulin, TTF-1 and CK7
are positive. CK20 is negative
• Kidney: RCC-Ma is positive. CK7 and
CK20 are negative
• Colon: CK20 and CDx2 are positive. CK7
and TTF-1 are negative
Clear cell hidradenoma
Endometriosis

• Metastatic melanoma can show epidermotropism
• The cells of metastatic lobular breast carcinoma have a linear array
between collagen bundles
Clinical Variants
• None
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CUTANEOUS INFILTRATES:
NON-LYMPHOID
Mast Cell Infiltrates
Mastocytosis
Introduction
Mastocytosis comprises a spectrum of related diseases in which there is an
increase in mast cells in one or more organs. It is classified into cutaneous
and systemic. Cutaneous mastocytosis includes: urticaria pigmentosa, solitary
mastocytoma, diffuse cutaneous mastocytosis and telangectasia macularis erup-
tive perstans (TMEP). Systemic mastocytosis can be with or without cutaneous
lesions.
Epidemiology 1. The infiltrate is predominately in the upper third of the dermis
• Although mastocytosis can occur at any 2. The number of mast cells depends on the clinical variant
age, usually the onset of mastocytosis is Other features:
in the first 2 years of life (50% or more • Eosinophils variably present
of the cases) • There are dense aggregates of mast cells in solitary mastocytoma and in some
• Gender distribution is approximately cases of urticaria pigmentosa. Loosely arranged mast cells are seen in diffuse
equal cutaneous mastocytosis. In TMEP there may be only subtle alterations and
only a few mast cells present
Pathophysiology
• Two Kit mutations have been demon-
strated which result in Kit autoactiva-
tion, and they are believed to be respon-
1
sible for increased number of mast cells
Mastocytosis
Mastocytosis CD117 staining
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Clinical features
• Urticaria pigmentosa (the most common
type) presents as a generalized eruption
of multiple red macules mainly on the
trunk. Less than 50% are pruritic
• Solitary mastocytoma may occur anywhere
on the body with a predilection for the
trunk
• Diffuse cutaneous mastocytosis is a rare
variant begins in early infancy with
Histological differential thickening of the skin, pruritus and blis-
1. Melanocytic nevi: tering are common
• S-100 positive • TMEP is a rare adult form of mastocytosis.
2. Langerhans cell histiocytosis: Telangectatic macules are found on the
• CD1a and S-100 positive trunk
• CD117 negative • More than 95% of adults but only a mi-
nority of children have systemic involve-
ment
Special studies
• Toluidine blue, Giemsa or chloroacetate
esterase
• CD117 (C-kit) and mast cell tryptase are
positive
Melanocytic nevus Langerhans cell histiocytosis
Clinical Variants
Important Things To Know • Urticaria pigmentosa
• Solitary mastocytoma
• Subepidermal vesiculobullos changes may be seen with mast cell lesions • Diffuse cutaneous mastocytosis
of infancy • Telangectasia macularis eruptive perstans
• Systemic mastocytosis (can be with or
without cutaneous lesions)
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Histiocytic Infiltrates
Juvenile xanthogranuloma
Introduction
Juvenile xanthogranuloma (JXG) is the most common non-Langerhans cell type
of histiocytosis. Usually it is a self-limited disease.

• JXG affects mostly children with most of 1. Diffuse collection of small monomorphous histiocytes are seen in the dermis,
the cases diagnosed in the first year of some of them with a foamy cytoplasm
life; however, similar lesions have been 2. Multitnucleated histiocytes (Touton cells)
reported in adults 3. Other inflammatory cells
Pathophysiology
• The etiology of JXG is unknown
Clinical features 1 2
• Yellow-red to brown papules, most com-

monly seen on the head and neck, but 2
can spread to the trunk and extremities
• A solitary lesion is seen in most of the
cases, 10% of the cases present with Juvenile xanthogranuloma Juvenile xanthogranuloma
multiple lesions

• CD68+, factor XIII a+, S-100–, CD1a– 1. Langerhans cell histiocytosis:
• Cells with eosinophilic cytoplasm and reniform (coffee bean) nuclei
• S-100+, CD1a+
Langerhans cell histiocytosis

Clinical Variants • Early JXG consists of numerous histiocytes with abundant cytoplasm.
• Benign cephalic histiocytosis Over time they become lipidized and Touton cells are identified
• Generalized eruptive histiocytosis
• Papular xanthogranuloma
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Xanthomas
Introduction
Xanthomas are group of infiltrates of foamy macrophages (histiocytes). They
are often associated with hyperlipidemias (eruptive, tuberous, tendinous and
xanthelasma) although others may be normolipemic (diffuse plane xanthoma,
verruciform, papular and plexiform). Epidemiology
• Papular xanthoma affects infants and
Histological features children, whereas plexiform type affects
1. Diffuse infiltrates of foamy histiocytes in the dermis middle-aged adult males. Other types
2. Variable numbers of other inflammatory cells have no age or sex predilection
Other features: Pathophysiology

• Eruptive xanthomas often have more inflammatory cells
• Multinucleated histiocytes are variably present in diffuse plane xanthomas • Xanthomas result when abnormalities in
and papular xanthomas the transportation of lipids (e.g. choles-
• In verruciform xanthomas, there is verrucous hyperplasia with parakerato- terol, triglycerides, and phospholipids)
sis and neutrophils cause these lipids to be deposited in the
• In plexiform xanthomas, nodular collection of foamy macrophages merge skin and being ingested by tissue macro-
with spindle-shaped cells arranged in large sweeping fascicles phages
Clinical features
• Yellow to brown papules, papules or
plaques, those associated with hyperlip-
idemias have characteristic sites: elbows
and knees (tuberous), Achilles tendon (
1
tendinous), eyelid ( xanthelasma), but-
tocks (eruptive)
• Diffuse planar xanthomas are distributed
2 periorbitally, on the trunk and extremi-
Xanthoma Xanthoma ties. Verruciform is a solitary lesion in
oral mucosa, papular xanthomas have a
generalized distribution while plexiform
Histological differential xanthomas involve the lower extremities
1. Langerhans cell histiocytosis:
• S-100+, CD1a+ Special studies
2. Juvenile xanthogranuloma: • CD68+, S-100–, CD1a–
• Foamy histiocytes are less prominent
Langerhans cell histiocytosis Juvenile xanthogranuloma
Clinical Variants
Important Things To Know • Tuberous xanthoma
• Xanthelasma is the most common form of xanthomas. Lipid levels are • Planar xanthoma
normal in around half of patients • Tendinous xanthoma
• Eruptive xanthoma
• Plexiform xanthoma
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Langerhans cell histiocytosis
Introduction
Langerhans cell histiocytosis (LCH) is a histioctytic disorder characterized by
proliferation and accumulation of Langerhans cells (LC) into a variety of organs.

• Although the disease can present at any 1. Clusters and sheets of large ovoid cells,
age, most often it presents within the immediately beneath the epidermis
1
first few years of life with a slight male 2. Cells with abundant eosinophilic cyto-
predominance plasm and a reniform and sometimes
coffee bean shaped nucleus
Pathophysiology 3. Focally the cells invade the epidermis,
• The etiology is unknown and there is forming small aggregates
considerable debate as to whether LCH Other features:
is a reactive disorder or a neoplastic • Variable admixture of other inflammatory
proliferation; however, the fact that the cells including: neutrophils, eosinophils, Langerhans cell histiocytosis
majority of cases studied have shown lymphocytes, and mast cells
clonal proliferation of LC supports the
latter hypothesis
Clinical features 3
• LCH can involve almost any organ

2
system
• In children, LCH mostly present with
multiorgan disease; however, adults more
frequently have single system disease
• Bone is the most commonly affected Langerhans cell histiocytosis CD1a staining
organ. Mucocutaneous lesions are the
second most common areas of involve-
ment, often presenting as a papulosqua- Histological differential
mous eruption 1. Juvenile xanthogranuloma:
• Prognosis is dependent upon the type • Multinucleated histiocytes (Touton cells)
and number of organs involved • No involvement of the epidermis
• CD68+, S-100–, CD1a–
Special studies 2. Xanthoma disseminatum:
• CD1a+, S-100+, langerin(CD207)+ • Mixture of histiocytes, foamy cells, multinucleated histiocytes
• CD68+, S-100–, CD1a–
Juvenile xanthogranuloma Xanthoma disseminatum
Clinical Variants Important Things To Know

• Letterer-Siwe disease • LC has Birbeck granules in cytoplasm detected by electron microscopy
• Eosinophilic granuloma
• Hand-Schuler-Christian disease
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Neuroendocrine Infiltrates
Merkel cell carcinoma
Introduction
Merkel cell carcinoma (MCC) is a rare malignant primary cutaneous neoplasm
with epithelial and neuroendocrine differentiation. The cell of origin remains
unresolved.

• The tumor most commonly affects white
Small, uniform round to oval blue cells with amphophilic sparse cytoplasm people
Other features: • Male-to-female ratio is 2.3:1
• Inconspicuous mitosis • It typically occurs on the
• Apoptotic bodies are abundant sun-exposed skin of older
• The tumor has three different histologi- adults
cal growth patterns, a sheet-like growth • MCC is highly aggressive
being the most common followed by malignancy with more
the nested and trabecular types. It is than 30% of patients dying
centered on the dermis and frequently within 5 years of diagnosis
extends into the subcutaneous fat Merkel cell carcinoma
Clinical features
• Solitary painless dome-shaped nodule
or indurated plaque. Red, violaceous or
1
skin-colored
• The most commonly affected sites are
the head and neck and extremities.
Pathophysiology
• Immunosuppression state and UV ir-
Merkel cell carcinoma CK20 staining radiation are risk factors
• Merkel cell polyoma virus (MCPyV)
Histological differential DNA was demonstrated to be monoclon-
ally integrated into the host genome in a
1. Basal cell carcinoma: majority of MCC
• Myxoid stroma
• Chromogranin and synaptophysin are
Special studies
negative • CK20 (paranuclear dots), AE1/AE3,
2. Metastatic small cell carcinoma: CAM5.2, chromogranin, and synap-
• TTF1 positive, MCPyV negative tophysin are positive
3. Lymphoma: • TTF1, CD45, S-100, and CK7 are nega-
• CD 45 positive, CK20 , chromogranin tive. Minority of CK20–/CK7+ cases
and synaptophysin are negative have been reported
Basal cell carcinoma • MCPyV positive in 80% of the cases
Important Things To
Know
• Epidermis maybe involved in a
pagetoid fashion
• Not infrequently, MCC occurs Lymphoma
in intimate association with an
Metastatic small cell carcinoma
in situ or invasive squamous cell
carcinoma
Clinical Variants
• None
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CUTANEOUS INFILTRATES:
LYMPHOID AND LEUKEMIC
Pseudolymphomas
Cutaneous pseudolymphomas
(lymphoid hyperplasia)
Introduction
Cutaneous pseudolymphomas are benign lymphoid proliferations which simu-
late cutaneous lymphoma clinically and histopathologically.

1. In lymphoid hyperplasia simulating B-cell
• It affects all age groups. Drug-induced lymphoma there is dense diffuse cellular
T-pseudolymphoma more frequently are infiltrate, which is more often “top heavy”.
seen in adults 1
Other Features:
Pathophysiology • Lymphoid follicles are present in many but
not all cases
• Reactive polyclonal proliferation of T and • Tingible bodies inside macrophages are
B lymphocytes. It may be induced by present
microbial, physical or chemical agents • Immunohistochemically, there is an
admixture of B and T lymphocytes with a
Clinical features predominance of T-cell lymphocytes. No
• Cutaneous lymphoid hyperplasia simulat- monocloanal populations are detected
ing B-cell lymphoma present as asymp- • In lymphomatoid drug reaction the infil-
tomatic red brown nodules or papules. trate may be band-like resembling mycosis
The most common sites of involvement fungoides or nodular
are the face, chest and upper extremities • Pseudolymphomatous folliculitis shows
• Lymphomatoid drug reaction take the diffuse predominantly perifollicular infil-
form of solitary plaques, nodules or mul- trate of lymphocytes with infiltration and
destruction of follicular structures Pseudolymphoma
tiple lesions with a wide spread distribu-
tion
• Pseudolymphomatous folliculitis present Histological differential
as solitary papule or nodule on the face 1. B-cell lymphoma:
• “Bottom-heavy” infiltrate
Special studies • Monoclonal populations are usually de-
• B-cell markers CD20 and CD79 are pres- tected
ent in some of the cells, while the T-cell • More than 50% of cells express B-cell
marker CD3 is present in the majority of markers
the cells. Polyclonal populations as dem-
onstrated with the lambda and kappa
light chains
• The germinal centers are highlighted by B-cell lymphoma
CD10 and BCL-6

• Presence of monoclonal populations is not an absolute diagnostic crite-
ria
• In reactions at site of vaccination, the subcutis is predominantly af-
Clinical Variants fected with little dermal involvement
• None
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Cutaneous Lymphomas
T-Cell lymphomas
Introduction
Heterogeneous group of neoplasms, which show considerable variation in
clinical presentation histopathology and prognosis. Mycosis fungoides (MF) is
the most common T-cell lymphoma.
1. MF patch stage shows atypical lymphocytes in the epidermis (epidermotro-
pism), typically confined to the basal layers either as single cells in a “string
of beads” arrangement or as small groups of cells (Pautrier collections)
• The nuclei of the lymphocytes are cerebriform. Sparse infiltrate of lympho-
cytes spread along the papillary dermis
• Frequently there is papillary fibrosis
• In the plaque stage, the infiltrate is denser
• In the tumor stage the epidermotropism is uncommon and the entire der-
mis is often involved
Epidemiology
• MF usually arises in late adulthood with
male predominance
1 Pathophysiology
• Neoplastic cells in MF are mature T cells
that express the cutaneous lymphocyte
antigen (CLA), which enables them to
specifically home into the skin.
• Etiology is unknown.
MF patch 2 MF patch 3
Clinical features
• MF is characterized by stepwise evolution
with sequential appearance of patches,
plaques and tumors. Pruritus is some-
times present. It has an indolent course
Special studies
1
• MF: CD3+, CD4+, CD8–, CD30–, loss of
CD5 and CD7
MF Plaque 2
MF Pautrier collections
MF tumoral 2
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1. Spongiotic dermatitis:
• Areas of spongiosis predominate with a few lymphocytes present in the epi-
dermis
• Lack of fibrosis of the papillary dermis
2. Drug reactions:
• May show similar features to MF, however, the lesions regress upon with-
drawal of the offending drug
Spongiotic dermatitis
Drug reaction
Clinical Variants
• Granulomatous
• Hypopigmented Important Things To Know
• Follicular • MF may show a protracted course and many times it takes several biop-
• Granulomatous slack skin syndrome sies before a final diagnosis can be established
• Papular
• Solitary
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Primary cutaneous CD30+ T-cell Epidemiology
lymphoproliferative disorders • LyP can affect
(lymphomatoid papulosis and

patients of any
age with peak
anaplastic large cell lymphoma) incidence dur-
ing the fifth
decade. No
Introduction major differ-
Lymphomatoid papulosis (LyP) and anaplastic large cell lymphoma (ALCL) are ence in gender distribution. Primary C-
chronic recurrent lymphoproliferative disease. The World Health Organization ALCL occurs in older adults and there is a
(WHO) classifies it within the spectrum of primary cutaneous CD30+ T-cell male predominance. It is the second most
lymphoproliferative disorders with cutaneous anaplastic large cell lymphoma common cutaneous T-cell lymphoma
(C-ALCL)
Clinical features
Histological features • Recurrent and self-regressing red papules
1. Diffuse infiltrates of atypical cells CD30+ present in and nodules. May occur singly or in
the dermis 1
crops
• Type A (Hodgkin-like) : wedge shape lesion with • The size of the lesions is usually less than
scattered, large , atypical CD4+/CD30+ cells in a 1.5 cm or 2 cm, but more commonly they
mixed inflammatory background are smaller
• Type B (MF-like): small to medium atypical CD4+
cells which are often CD30 negative Pathophysiology
with scant inflammatory background • Whether LyP and C-ALCL represent
and marked epidermotropism indolent lymphomas. In both entities are
• Type C (ALCL-like): sheets of large characterized by t(2;5)(p23;q35)
atypical CD4+/CD30+ cells
• Type D (Berti-like): sheets of medium
and large sized atypical CD8+/CD30+
Special studies
cells with scant or none inflammatory • Variable expression of CD4, CD8 and
background and moderate epidermotro- CD30 depends on the histologic type
pism by small and large cells Lymphomatoid papulosis
• Type E shows angiocentric infiltrates
Histologic differential
1. Mycosis fungoides with large cell trans-
formation:
• Patches or plaques clinically
• Band-like or diffuse infiltrate
• Moderate to marked epidermotropism
• Focal CD30 positivity
2. Arthropod bites:
• Diffuse infiltrate composed of lympho- Mycosis fungoides
CD 30 Staining
cytes and numerous eosinophils
• CD30–
3. Pityriasis lichenoides et varioliformis
acuta (PLEVA):
• Areas of parakeratosis
• Dyskeratotic keratinocytes
• Absence of CD30+ cells
Arthropod bite
Pityriasis lichenoides et varioliformis
Important Things To Know acuta
• Systemic and C-ALCL can be differentiated by the use of ALK stain,
which is positive in the systemic variant and negative in C-ALCL Clinical Variants
• None
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Epidemiology B-cell lymphoma 1
• Primary
cutaneous Introduction
marginal Cutaneous follicle center cell lymphoma and
zone lympho- extranodal marginal zone B-cell lymphoma 2
ma (PCMZL) represent 90% of all forms of cutaneous
and primary B-cell lymphomas. Other cutaneous B-cell
follicle center lymphomas are diffuse large B-cell lympho-
cell lymphoma occur in adults mas (DLBCL) of leg type, intravascular B-cell Primary cutaneous marginal
• PCMZL has a male predominance. lymphoma and mantle cell lymphoma. zone lymphoma (PCMZL)
DLBCL, leg type has a female predomi-
nance Histological features
Pathophysiology 1. PCMZL shows a dermal cellular infiltrate
that may extend into the subcutis but
• PCMZL and DLBCL, leg type arise from spares the epidermis
post germinal center B-cells, primary cu- 2. It has a nodular or diffuse pattern char-
taneous follicle center lymphoma arises acterized by reactive lymphoid follicles
32
from mature germinal center B-cells surrounded by paler zone

Clinical features Other features:
• They contain a mixed population of cells: Follicular lymphoma
• PCMZL occur mainly on the arms and small lymphocytes, centrocyte-like cells,
trunk but other sides such as the head monocytoid B-cells, lymphoplasmacytoid
and neck may also be involved. The cells and plasma cells
lesions are red to purple papules or • Follicular lymphoma may show follicular,
nodules follicular and diffuse, or diffuse patterns.
• Lesions of follicle center lymphoma are Follicles are often variable in size and
usually single erythematous plaques or may fuse together. The follicle centers
tumors; occur on the head and neck and contain varying proportions of large and
trunk small centrocytes with cleaved nuclei and
• DLBCL, leg type occurs most frequently centroblasts with noncleaved nuclei and
on the leg (72%) but can occur at other prominent nucleoli. Tangible body macro-
sites. The lesions present as rapidly phages are absent
growing erythematous tumors • DLBCL shows a diffuse infiltrate in the
dermis and subcutis of large lymphocytes
Special studies with features of centroblasts and immuno-
• PCMZL: CD20+, CD79a+, bcl-2+, CD5–, blasts, mitotic figures are common
CD10–, CD43–, cyclin D1– • Other types of DLBCL in the skin are
• There is cytoplasmic immunoglobulin intravascular large B-cell lymphoma, plas- Diffuse large B-cell lymphomas
light chain restriction mablastic lymphoma, DLBCL leg type (DLBCL)
• Follicle center lymphoma: CD20+,
CD10+, bcl-6+, bcl-2 is negative Histological differential
• DLBCL: CD20+, CD 79a+, bcl-6+, bcl-2+, 1. Pseudolymphoma:
MUM1/IRF4+ • Usually top heavy versus bottom heavy in lymphomas
• Lymphoid follicles have obvious tangible body macrophages
• Plasma cells in pseudolymphoma are polyclonal and monoclonal in PCMZL

Pseudolymphoma • Plasmacytoid cells are a clue to PCMZL
• Unlike follicular lymphoma of lymph nodes, the t(14:18) is not found in
Clinical Variants primary cutaneous cases
• None
110
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Leukemic and Miscellaneous Infiltrates
Leukemia cutis
Introduction
Cutaneous infiltrate of leukemic cells of acute or chronic myeloid leukemias
(AML and CML, respectively), lymphoid leukemias, and in the setting of my-
elodysplastic and myeloproliferative syndromes.
Epidemiology
Histological features • Cutaneous involvement in AML is in the
1. Sheets of atypical cells involve the dermis range of 2–20%, particularly M4 and M5,
and subcutis and in CML, 0–4%. Males and females
Other features: are equally affected, mostly adults
1 • Precursor B-cell leukemia/lymphoma
• There may be destruction of the append-
ages by periappendageal infiltrate (PBLA) is more common in the skin than
• Sometimes there is percolation between those of precursor T-cell origin (PTLA).
collagen bundles in an “Indian file pat- Children are mostly affected. Skin is
tern” involved in 2% of chronic lymphocytic
• In CML the infiltrate is more pleomor- leukemia/small lymphocytic lymphoma (
phic with immature and mature granu- CLL/SLL)
locytes
• In PBLA the infiltrate consist of medi- Pathophysiology
um-sized lymphoid cells with round • Leukemia arises from hematopoietic
or convoluted nuclei, inconspicuous stem cells in the bone marrow. Down
nucleoli and scant basophilic cytoplasm syndrome and Fanconi anemia predis-
• Mitosis and apoptotic bodies are often pose to AML. CML associated with t
seen (9:22)
• CLL/SLL: diffuse or nodular infiltrate of Leukemia cutis • CLL/SLL and PBLA are of B-cell origin
small mature lymphocytes
Clinical features
Histological differential • Myeloid leukemia present as single or
1. T-cell lymphomas: multiple macules, papules, nodules or
• T-cell markers are positive CD3, CD4 or CD8 plaques with red/brown color in no
2. Merkel cell carcinoma: particular distribution. Gum infiltration
• Negative lymphoid markers is common in M5
• Positive for CD20 and polyoma virus • PBLA and PTLA: erythematous papules
or nodules mostly on the head and neck
Special studies
• Myeloid leukemia: myeloperoxidase,
CD43+ CD11+, lysozyme+. CD3–, CD20–
• PBLA: CD45+, CD79a+, CD10+, CD99+,
Tdt+, CD20+ less commonly
• CLL/SLL: CD45+, CD20+, CD5+,
CD23+, CD10–, cyclinD1–
T-cell lymphomas Merkel cell carcinoma

• Leukemia in biopsies show superficial and deep infiltrate with periec-
crine and perivascular distribution. “Indian file pattern” is a clue in
myeloid leukemia
Clinical Variants
• None
111
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neuromas 8 Vascular Tumors
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Infantile hemangiomas
Cutaneous ganglioneuroma Johnston RB. Weedon’s Skin Pathology Essentials. Edinburgh:
Bolognia J, Jorizzo J, Schaffer J (eds) Dermatology 3e. Elsevier/Churchill Livingstone; 2012: 594.
Philadelphia: Elsevier/Saunders 2012. Kempf W, Hantschke M, Kutzner H, Burgdorf W.
Calonje E, Brenn T, Lazar A, McKee PH. McKee’s Pathology of Dermatopathology. New York: Springer; 2008:262–3.
the Skin with Clinical Correlations, 4e. Edinburgh: Elsevier/ Sangueza OP, Requena L. Pathology of Vascular Skin Lesions:
Saunders; 2012. Clinicopathologic Correlations. New York: Humana Press;
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Weedon D. Skin Pathology 2e. Edinburgh: Elsevier/Churchill Cherry angiomas
Livingstone; 2002. Sangueza OP, Requena L. Pathology of Vascular Skin Lesions:
Clinicopathologic Correlations. New York: Humana Press;
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Bolognia J, Jorizzo J, Schaffer J (eds) Dermatology 3e.
Philadelphia: Elsevier/Saunders 2012. Arteriovenous hemangioma
Calonje E, Brenn T, Lazar A, McKee PH. McKee’s Pathology of Sangueza OP, Requena L. Pathology of Vascular Skin Lesions:
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Calonje E, Brenn T, Lazar A, McKee PH. McKee’s Pathology of Sangueza OP, Requena L. Pathology of Vascular Skin Lesions:
the Skin with Clinical Correlations, 4e. Edinburgh: Elsevier/ Clinicopathologic Correlations. New York: Humana Press;
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Granular cell tumor
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Clinicopathologic Correlations. New York: Humana Press; expression indicates a low-grade carcinoma profile.
2003: 174–76. Histopathology 2001;38:454–7.
Kaposiform Dermoid cyst

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Sangueza OP, Requena L. Pathology of Vascular Skin Lesions: 2e. New York: McGraw-Hill 2004: 564–7.
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2003: 177–81. 2005: 253–5.
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1822–3.
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Elsevier/Churchill Livingstone; 2012: 707. Synopsis of Clinical Dermatology 5e. New York: McGraw-Hill;
North PE, Kincannon J. Vascular neoplasms and neoplastic-like 2005.
proliferations. In: Bolognia J, Jorizzo J, Schaffer J. Dermatology
(eds) Dermatology 3e. Philadelphia: Elsevier/ Saunders 2012: Steatocystoma
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Elsevier/Churchill Livingstone; 2012: 712. Stone MS. Cysts. In Bolognia J, Jorizzo J, Schaffer J.
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9 Cutaneous Cysts Dermatology 3e. Philadelphia: Elsevier/Saunders; 2012: 1824.

Epidermoid cyst Hill; 2005.
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2e. New York: McGraw-Hill 2004: 563. Cutaneous ciliated cyst
Rapini R. Practical Dermatopathology. St Louis: Elsevier/Mosby; Barnhill RL, Crowson AN (eds). Textbook of Dermatopathology
2005: 253. 2e. New York: McGraw-Hill 2004: 564–9.
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3e. Philadelphia: Elsevier/Saunders; 2012: 1817–23. 2005: 256.
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2005: 199. Wolff K, Johnson RA, Suurmond D. Fitzpatrick’s Color Atlas
Pilar cyst Hill; 2005.
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neoplasms–part 1: an approach to tumours of the Median raphe cyst
pilosebaceous unit. J Clin Pathol 2007;60:129–44. Barnhill RL, Crowson AN (eds). Textbook of Dermatopathology
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Dermatology 3e. Philadelphia: Elsevier/Saunders; 2012: 12 Cutaneous Infiltrates,
1824–5.
Lymphoid and Leukemic
Hill; 2005. Cutaneous pseudolymphomas
(lymphoid hyperplasia)
10 Cutaneous Metastases LeBoit PE, Burg G, Weedon D, Sarasain A (eds). World Health
Orgnization Classification of Tumors. Pathology and Genetics
of Skin Tumors. Lyon: IARC Press; 2006: 213–4.
Weedon D. Weedon’s Skin Pathology 3e. Edinburgh: Elsevier/ Weedon D. Weedon’s Skin Pathology 3e. Edinburgh: Elsevier/
Churchill Livingstone; 2010: 928–33. Churchill Livingstone; 2010: 1000–2.
11 Cutanous Infiltrates, T-cell lymphomas

Non Lymphoid LeBoit PE, Burg G, Weedon D, Sarasain A (eds). World Health
of Skin Tumors. Lyon: IARC Press; 2006: 170–91.
Mastocytosis Weedon D. Weedon’s Skin Pathology 3e. Edinburgh: Elsevier/
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Churchill Livingstone; 2010: 947–9. lymphomas: a retrospective case series of 84 patients. Clin
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overview of the most common histiocytic disorders. G Ital
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Xanthomas of Skin Tumors. Lyon: IARC Press; 2006: 195–99.
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Churchill Livingstone; 2010: 961–3. Orgnization Classification of Tumors. Pathology and Genetics
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Glossary of Terms
Epidermal e. Hypogranulosis - decreased granules in the keratino-
cytes of the stratum granulosum
a. Hyperkeratosis - thickening of the stratum
corneum
Hyperkeratosis
} Hypogranulosis
f. Hyperplasia - an increased number of cells

b. Orthokeratosis - ‘basket-weave’ appearance of i. Psoriasiform - regular acanthosis with elongated rete
the stratum corneum without retention of ridges of the same length
keratinocyte nuclei
Orthokeratosis Psoriasiform
hyperplasia
}
ii. Irregular - acanthosis with rete ridges of differing
lengths, often pointed
c. Parakeratosis - the retention of nuclei by keratinocytes
}
in the stratum corneum Irregular
hyperplasia
}
Column of with pointed
parakera- Ortho- rete ridges
tosis with keratosis
surrounding iii. Papillated - thickening of the epidermis with nipple-
like elevations
ortho-
keratosis
Papillated
hyperplasia
d. Hypergranulosis - increased granules in the keratino-
cytes of the stratum granulosum
iv. Pseudocarcinomatous - extreme, irregular thicken-
ing of the epidermis with increased mitoses, squamous
eddies, or keratin pearls which may mimic squamous cell
Hypergranulosis carcinoma.
Irregular
}
Keratin epidermal
pearl hyperplasia
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1. Squamous eddy - concentric, whorled groups of j. Ballooning - intracellular edema that eventually causes
keratinocytes with increased keratinization towards the loss of attachment to adjacent cells (secondary acantholy-
center sis), generally due to viral particles
}
Ballooning
Squamous degeneration of
eddy epidermal cells
2. Horn (or keratin) pearl - a squamous eddy with more

abrupt and complete keratinization
Keratin
pearls k. Acantholysis - the loss of cohesion between
keratinocytes due to dissolution of intercellular connec-
tions (desmosomes) (see Dyskeratosis photo)
l. Spongiform pustule - collections of neutrophils in the

spinous layer
g. Acanthosis - diffuse epidermal hyperplasia,

especially of the stratum spinosum
Spongiform pustules
Acanthosis }
h. Atrophy - decreased thickness of a tissue or layer m. Dyskeratosis - abnormal or premature
cornification of keratinocytes
Epidermal
atrophy with }
loss of rete Dyskeratosis
ridges and Acantholysis
dermal papilla
pattern
i. Spongiosis - intercellular edema expands the space
between keratinocytes and can cause the cells to become n. Necrosis - cell death with subsequent
elongated or stretched degeneration
Spongiosis and Necrosis

formation of
intraepidermal
vesicles
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o. Vacuolar alteration - intracellular or extracellular clear c. Lymphohistiocytic infiltrate- a collection of lympho-
space that causes damaged keratinocytes to appear vacu- cytes and histiocytes
olated
Mixed infiltrate
Vacuolar of lymphocytes
alteration and histiocytes
in pigmented
purpuric
dermatosis
p. Clefts - an empty space, which may contain fluid,

lipid, or other substances that is lost during tissue pro-
cessing d. Lichenoid infiltrate - a band-like configuration of
inflammatory cells arranged parallel to the dermis
}
Cleἀ
Band-like,
lichenoid in-
filtrate seen in
q. Interface dermatitis - liquefactive degeneration of the lichenoid drug
basal cell layer at the interface between the epidermis reaction
and dermis with sparse inflammation
e. Nodular infiltrate - dense discrete aggregations of
inflammatory or tumor cells
Interface
}
dermatitis
with vacuolar
change
Nodular
malignant
melanoma
Dermal
a. Monomorphous infiltrate - abnormal presence of f. Leukocytoclastic infiltrate - collection of
inflammatory cells of one cell type abnormal neutrophils characterized by chromatin
fragmentation, nuclear dust, and necrotic debris
Pseudo-
lymphoma Nuclear dust
composed pre-
dominantly of Infiltrate of
lymphocytes abnormal
neutrophils
b. Mixed infiltrate - abnormal presence of inflammatory g. Diffuse infiltrate - an infiltrate of inflammatory or
cells of multiple cell types tumor cells distributed in a nonlocalized fashion
Mixed infiltrate
of lymphocytes,
}
histiocytes, and
eosinophils in Diffuse infiltrate in
urticarial superficial and deep
pemphigoid dermis
123
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Connective Tissue d. Sclerosis - an increase in collagen with either a nor-
mal or decreased number of fibroblasts
}
a. Collagen degeneration - disorganized, fragmented
mass of collagen (as opposed to the tightly packed, Thickened collagen
strictly aligned filaments normally seen) throughout the
Collagen dermis with
degeneration decreased
alternating with cellularity
areas of
perivascular
infiltrate e. Collagen in vertical streaks - a vertical orientation of
thick collagen bundles that occurs with chronic rubbing
b. Hyalinization of collagen - relatively hypocellular,

eosinophilic appearance of collagen Vertically
Hyalinized collagen streaked collagen
within the
with hypocellularity papillary dermis
} More regular
appearance of
} collagen compared to
affected area above f. Lamellated collagen - layered, or plate-like arrange-
ment of collagen
c. Fibrosis - an increase in collagen associated with an
increased number of fibroblasts
Whorls of
Increased layered collagen
collagen with surrounding
an increased areas of
number of increased
fibroblasts (at melanocytes
tip of lines)
124
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Dermatopathology Primer of Cutaneous Tumor

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Who are the authors of the book?

Who are the authors of the book?

What topics are covered in the histology section?

What topics are covered in the histology section?

Dermatopathology

Primer of Cutaneous Tumors

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Omar P. Sangueza, MD Parisa Mansoori, MD

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No claim to original U.S. Government works

International Standard Book Number-13: 978-1-4987-0392-5 (eBook - PDF)

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• Genetic mosaicism is thought to be the 3. Hyperkeratosis

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1. Well-circumscribed lesions composed of uniform pale keratinocytes Pathophysiology

Important things to know

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Epidemiology Histological features

Clinical features Wart 2

Seborrheic keratosis Verrucous squamous cell carcinoma

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Important Things To Know

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Histological features Epidemiology

Histological differential Clinical features

Important Things To Know

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• Sharply defined, tan to black, flat, 1

Special studies Histological differential

Epidermal nevus Squamous cell carcinoma

Clinical variants Important Things To Know

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Histological features Clinical features

Familial benign pemphigus Darier’s disease Pemphigus vegetans

Important Things To Know

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superficial basal cell carcinoma Morpheaform or infiltrative

Important Things To Know

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Epidemiology Histological features

Clinical features Bowen Disease

Important Things To Know

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Histological features Epidemiology

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Hypertrophic atypical Keratoacanthoma

Important Things To Know

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• The etiology is unknown

Clinical features Histological differential

Solar lentigo Junctional nevus

Important Things To Know

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Histological features Epidemiology