Pansitopenia

Pansitopenia
What's pancytopenia?
Its combination of anemia , leukopenia and
thrombocytopenia
1.HB < 10 g/dL
2.Leukocyte count < 4000/ul
Absolute Neutrophil count <1500/uL
3.Platelet count < 150,000 uL
What's causes of
pancytopenia?
 Bone marrow failure : aplastic anemia
 Bone marrow infiltration :
 Acute leukemia
 Myeloma
 Lymphoma
 Carcinoma
 MDS
 Ineffective haematopoiesis
 Megaloblastic anaemia
 AIDS
 Peripheral pooling / destruction
 Hypersplenism: portal hypertension ,
felty's syndrome , malaria , Myelofibrosis
 SLE
What's approach to
thrombocytopenia?
 History
 Examination
 CBC & blood film
 BM aspiration & biopsy
 Other specific investigation

History
 Duration of symptom
 Long (MDS)
 Short (aplastic
anemia)of transfusion
 History
 History of hemoglobinurea
 Dietary history
 Exposure to drugs : anti cancer , Abs , anti
thyroid (aplastic anemia)
 Barbiturates , phenytoin ( B12, Folic acid)
 Chemotherapy , radiation ( MDS , AML)
 Weight loss , fever ( Inflammatory or
malignancy)
 Jaundice ( Hepatitis B or C)
 Joint pain (SLE)
 History of blood loss
General examination
 Eye examination: retinal hemorrhage
leukemic infiltrations
 oral examination : oral petechaie
stomatitis / chelitis
gum hyperplasia
oral candidiasis
 Respiratory examination : clubbing
tachypnea
 Abdominal examination : organomegaly
lymphadenopathy
 skin examination : malar rash
purpura
hypo or
hyperpigmentation
 Musculoskelatal system : short stature
synovitis
abnormal thumb
Pancytopenia + Absent thumb
+Child
 Pancytopenia + Back pain +
Hypercalcemia
(multiple myeloma)
 Pancytopenia + Malar rash or GN = SLE
 pancytopenia + HSM = Leukemia

Blood Film
1.RBC morphology ( size & shape)
2.WBC and RBC precursor
3.Platelets count & size
4.Abnormal increase or decrease
granulation in Neutrophil
5. Hypo / hypersegmented
Neutrophil
Other evaluating test may be
included
 ESR
 Reticulocyte count
 Serum LFTs
 Hepatic serology
 Serum coagulation profile,
bleeding time, fibrinogen, and D-
dimer
 Serum
 B12 and folate
HIV test
Anisocytosis--different sized
RBCs
Poikilocytosis--differently
shaped RBCs
Platelets are small, and
reduced in numbers
Aplastic anemia
Macrocytosis
Howel jolly bodies
Basophilic stippling
Hypersegmented Neutrophil
Megaloblastic anemia
Tear drop cells
Hypogranular neutrophils
Pseudo pelger Heut Anoma y

l
Giant platelets
MDS
 The characteristic peripheral blood
morphologic feature in multiple
myeloma is:
A. Cytotoxic T cells
B. Rouleaux formation
C. Spherocytosis
D. Macrocytosis
True or false?
 Inblood film normal platelets count
rules out aplastic anemia
 True
Bone Marrow Examination
Almost always indicated in case
pancytopenia unless cause is apparent.
Both aspiration and biopsy are indicated.
Specifically, bone marrow aspirate permits
examination of:
• Cytology (megaloblastic change,
dysplastic changes, abnormal cell
infiltrates)
• Immunophenotyping : antigen or marker
on cells surfaces e.g ( leukemias,
lymphoproliferative disorders)
• Cytogenetics : structure of
(myelodysplasia,
chromosome leukemias,
lymphoproliferative disorders).
True or false?
 Bone marrow examination is required
in diagnosis of Megaloblastic anemia
 False
The differential diagnosis of pancytopenia
are based on cellularity of bone marrow :
 Hypocellular: excessive amount of fat

cells
 Normocellular: 50-70% hematopoietic

cells & 30-50% fat
 Hypercellular: 80-100% cells with little

Hypercellular
Causes of pocellular BM
Hy
1.Aplastic anemia
2.Hypoblastic MDS
3.Cytotoxic agent & radiotherapy

Causes of ercellular BM with
Hyp
primary marrow disorders
1.Acute leukemia / lymphoma
2. Hairy cell leukemia
3. Myelofibrosis
4.PNH
5.Mutiple myeloma
6. Mylodysblastic leukemia
Causes of ercellular BM with
Hyp
systemic disorders
1.Metastatic solid tumor
2. hypersplenism
3.Megaloblastic anemia
4. Infection (T.B ,kala azar, brucellosis)
5. Overwhelming infections
6. Alcohol
7. Autoimmune disorders- SLE, Sjogren’s
8. Sarcoidosis
9. Storage disease- Gaucher, Niemann-
pick
Pancytopenia +markedly
Hypocellular scattered mature
lymphocytes
aplastic anemia
Pancytopenia + Hypercellular
BM
Infiltration by RS cells HL
B.M + old age
MDS
marrow
Infiltration with malignant cells (Metastasis)

Specific investigations
 Megaloblastic anemia: Vit.B12 , Folate
assay
 Multiple
myeloma :
Imunoelectrophoresis
 PNH: Flow cytometry (CD55, CD59)
 Leishmaniasis: blood and bone
marrow culture, serum ELISA
 HIV ,EBV , hepatitis : virology screen
 Fanconi anemia :
Chromosomal breakage study

Pansitopenia

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Pansitopenia

 CBC & blood film

 BM aspiration & biopsy

 Other specific investigation

 Pancytopenia + Malar rash or GN = SLE

 pancytopenia + HSM = Leukemia

Howel jolly bodies

Pseudo pelger Heut Anoma y

 Hypocellular: excessive amount of fat

 Normocellular: 50-70% hematopoietic

 Hypercellular: 80-100% cells with little

3.Cytotoxic agent & radiotherapy

2. Hairy cell leukemia

Infiltration with malignant cells (Metastasis)

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