Some Misconceptions and Pitfalls in Ultrasonography
Some Misconceptions and Pitfalls in Ultrasonography
Some Misconceptions and Pitfalls in Ultrasonography
Summary: There are many misconceptions in the field of ultrasonography. Some are
because of poor understanding of anatomy and/or embryological or developmental
features of certain organs, which have prevailed over the course of the centuries since
the discovery of these entities (e.g., column of Bertin and hypertrophic column of
Bertin). Some misconceptions derived from misinterpretation (e.g., double decidual
sac sign) or inadequate observation of ultrasonographic findings. (e.g., hyperechoic
stroma in polycystic ovarian syndrome). Key Words: Hypertrophic column of
Bertin—Milk of calcium–Renal cyst—Double decidual sac sign—Hashimoto thyroid-
itis—Polycystic ovarian syndrome.
Objectives: After reading this article and completing the embryologic development of the kidney. The adult kidney
posttest, the learner should be able to: consists of approximately 14 lobes. During early fetal life,
● Summarize the anatomic detail and some developmental such lobes are like small individual kidneys called reniculi
features of certain common misconceptions of entities in (or renunculi) (Fig. 2). Each reniculus is like a small kidney
the kidney, early pregnancy, thyroid, ovary, diaphragm, that consists of its own cortical and medullary tissues and its
and abdominal aorta. own blood supply and collecting system. The central med-
● Describe ultrasonographic findings based on a better un- ullary tissue (pyramid) is enveloped on all sides by cortical
derstanding of the aforementioned anatomy, therefore tissue, except where the papilla (i.e., the tip of the pyramid)
avoiding misdiagnosis and achieving accurate diagnosis emerges. There are two parts to the cortical tissue: 1) cen-
of these entities. trilobe cortex (cortical arch)3 that covers the base of the
pyramid; and 2) mural cortex that wraps around the sides of
There are a few misconceptions pertaining to the column of
the pyramid. When the reniculi fuse to form a single kidney,
Bertin and renal lobes. The term “column of Bertin” is a
the centrilobar cortex of adjacent reniculi fuse to form the
misnomer. When French anatomist Dr. Exupère Joseph
renal cortex, whereas the mural cortices of adjacent reniculi
Bertin1 first described the cortical tissue between pyramids
fuse to form the cloisonné (septum) of Bertin. Because mu-
in 1744, he called it cloisonné, which means partition or
ral cortices surround each pyramid, when multiple reniculi
septum. However, the term “cloisonné” was mistranslated
fuse together, mural cortices naturally form honeycomb-like
as column in English, and column of Bertin remains popu-
partitions.
lar. Hodson’s1 attempt to revert it back to being called the
There are numerous lobules within the renal cortex and
cloisonné of Bertin was in vain. Only a few people referred
septum of Bertin, approximately 20,000 lobules in the entire
to it as the septum of Bertin.2 It is evident that the column
kidney.3 The lobules radiate from the surface of the pyramid
is not the real feature of this structure if one look at a
outward in each reniculus; hence, in an adult kidney, the
tangential section of the kidney cortex (Fig. 1). The cortical
lobules are perpendicular to the renal surface within the
tissue between the pyramids form a honeycomb-like parti-
renal cortex but parallel to the renal surface within the septa
tion, and the pyramids are embedded within this honey-
of Bertin. The lobules contain renal tubules (cortical rays or
comb. This can also be easily understood if one studies the
medullary rays of Ferrin).3 Within the interlobular spaces
are straight interlobular arteries and veins. Along the surface
of the pyramid are arcuate arteries that give rise to inter-
The author has disclosed that he has no significant relationship with or
financial interest in any commercial companies pertaining to this educa- lobular arteries.
tional activity.
Address correspondence and reprint requests to: Dr. Hsu-Chong Yeh, HYPERTROPHIC COLUMN OF BERTIN
Department of Radiology, Box 1234, Mount Sinai—NYU Medical Center,
One Gustave L. Levy Place, New York, NY 10029. E-mail: hsu- A 2- to 3-cm mass-like structure is not uncommonly seen
chong.yeh@mountsinai.org in the kidney, usually at the junction between the upper and
129
130 H. C. YEH
literature. Because a pyramid (the tip of which is the papilla) from the upper pole to the lower pole, and from one side to
surrounded by cortical tissue forms a renal lobe, the term the other on sagittal or coronal scanning, we have found
“lobar dysmorphisor” was coined based on this finding in- many kidneys that appear to form by fusing of the superior
dicating that this is a large and malpositioned renal lobe. and inferior kidneys.20 We called these two kidneys supe-
The eighth feature is an ancillary sign that is seen in some rior and inferior subkidneys. The upper pole of the inferior
cases when the junctional parenchyma extends to the medial subkidney usually overlaps the lower pole of the superior
side of the kidney. subkidney. The former is located anterior to the latter at the
The so-called hypertrophic column of Bertin actually rep- area of overlap. The so-called hypertrophic column of
resents unresorbed polar parenchyma of either the superior Bertin represents unresolved renal parenchyma at the junc-
or inferior subkidney20 (Figs. 3–5), and not a single large tion of two subkidneys; therefore, we call it junctional pa-
septum of Bertin. After studying 15- to 30-mm thick em- renchyma.20 Within the junctional parenchyma, there are
bryo resin cases of the kidney, Fine and Keson21 found that normal renal cortex, pyramids, and septa of Bertin. Between
most kidneys develop by means of fusion of two kidneys the two subkidneys, an echogenic line may be seen. This is
(upper and lower ones), which correspond to the upper and called the junctional parenchymal line.20 A groove on the
lower groups of calyces. Although calyces are not usually surface of the kidney formed by this line appears as a small,
clearly delineated in ultrasonography, the echogenic renal triangular defect that is called the junctional parenchymal
sinus fat in which the calyceal system is situated can be defect. When all elements and features of junctional paren-
clearly seen by ultrasonography in a normal kidney. A kid- chyma (e.g., renal cortex, pyramids, septa of Bertin, junc-
ney is composed of echogenic sinus fat enveloped by renal tional parenchymal line, and junctional parenchymal defect)
parenchyma. The renal parenchyma consists of renal cortex, are identified and two fused subkidneys are recognized on
pyramids, and septa of Bertin, which are all less echogenic ultrasonography, the diagnosis of junctional parenchyma
than the renal sinus fat. By carefully scanning the kidney can be certain, and a tumor can be excluded. Even if two
usually difficult to perform unless the kidney is horizontally ally round. Color Doppler may show no detectable flow or
oriented, and ultrasound scanning may not show good detail symmetrical vascular supply from adjacent arcuate vessels
of the parenchymal tissue in the middle portion of the kid- without any irregular tumor vessels.
ney. A typical normal septum of Bertin is pear-shape, with
a small part pointing toward the renal surface20 (Fig. 10). A
large or hypertrophic septa of Bertin retains a pear-shape FETAL LOBATION, RENAL SCARS, CORTICAL
and is highly echogenic20 (Fig. 11). It is always located TUMOR, AND HYPERTROPHIC RENAL LOBE
between two pyramids and usually partly protrudes into the
renal sinus. It may sometimes indent on the adjacent pyra- It is well known that so-called fetal lobulation is a normal
mids on both sides (Fig. 12). A single or double hypertro- variation of the kidney in which the lobular contour of the
phic septa of Bertin may be seen. It is usually located in the fetal kidney remains in the adult kidney. In fact, as previ-
anterior parenchyma in the middle portion of the kidney. ously mentioned, a kidney consists of approximately 20,000
This is different from junctional parenchyma, which is usu- lobules and 14 lobes. There are numerous lobules in each
ally located at the junction between the upper and middle lobe. The renal lobules are too small to be delineated by
third of the kidney and between two renal sinus systems on ultrasonography. What we see in fetal kidneys are lobes,
transverse scanning and along the lateral aspect of the kid- and the term “fetal lobulation” should, instead, be “fetal
ney. The characteristic pear-shape, homogeneous high-level lobation.” Although the term “lobulation” has been used to
echoes, and location between two adjacent pyramids usually describe a bumpy or undulated contour of an object, e.g., a
allow the diagnosis of a true hypertrophic septum of Bertin lobulated tumor, and is not necessarily related to true lob-
and differentiate it from an echogenic tumor, which is usu- ules. Hence, fetal lobulation may mean that kidney has an
undulated contour similar to a fetal kidney, whereas fetal MILK OF CALCIUM IN A RENAL CYST
lobation means that a kidney retains a multiple lobar con- Milk of calcium in a renal cyst or calyceal diverticulum
tour similar to a fetal kidney; certainly, this is a much more had been considered to be exceedingly rare25 and, therefore,
precise term and was coined by Hodson.1,24 only a few case reports26–30 had been published because of
The diagnosis of fetal lobation can be made by finding its rarity until 1992, which is when we found that this is
that each bulge of the undulated renal contour corresponds actually common.31 Because milk of calcium contains cal-
to each renal lobe. Because each renal lobe is formed by a cium, naturally, layering of highly echogenic material with
pyramid surrounded by cortical tissue, each bulge on the an acoustic shadow was thought to be the ultrasonographic
renal contour should correspond to a renal lobe, i.e., each feature of this entity. In fact, in most instances, milk of
bulge should overlie one pyramid and each indentation calcium does not cast an acoustic shadow because it is usu-
should be between two lobes (Fig. 13). This is different ally seen in small renal cysts, smaller than 1cm and only
from renal scars, which may also result in indentations (or occasionally larger than 1.6 cm. Each cyst usually contains
cortical defects) and undulation on the renal contour. The only a small amount of milk of calcium, which produces
indentation (or indentations) from the scar is more likely to reverberation echoes (Fig. 17). This phenomenon can also
be located in the middle of a bulge (a renal lobe) on the occur with other small, highly reflecting particles, such as
renal contour or in a random fashion, rather than in between cholesterol crystals and ground sand. The reverberation ech-
two lobes (Fig. 14). A small tumor may also cause a bump oes are caused by the ultrasound beam bouncing back and
on the renal contour (Fig. 15). In diagnosing fetal lobation, forth within the aggregations of small, highly reflecting par-
one should carefully examine each bulge on the renal con- ticles. When there is a larger amount of milk of calcium,
tour to be certain that each bulge corresponds to each renal part of the sound beam will be absorbed or scattered away
lobe so that a renal mass associated with fetal lobation may from the transducer, and partial shadowing may occur.
not be missed. When cysts are larger than 1.2 cm, more apparent acoustic
A hypertrophic renal lobe may simulate a renal cortical shadowing may be seen, and cysts smaller than 0.6 cm
tumor (Fig. 16). Careful scanning to delineate the pyramid usually have no acoustic shadowing. In a larger cyst, the
within it and the symmetrical echogenic septa of Bertin on acoustic shadow will become more obvious as the layer of
both sides will allow a diagnosis of a hypertrophic renal milk of calcium increases in thickness. If one partly aspi-
lobe. rates the cystic fluid, the cyst becomes small, and the layer
FIG. 12. True hypertropic septa of Bertin compressing on pyramids. FIG. 13. Fetal lobation. A. Right kidney of a 35-week-old fetus. Note
Sagittal scan of the kidney shows two markedly enlarged septa of Bertin undulated renal contour caused by renal lobes (arrows). B. Similar lobation
(arrowheads) that indent on adjacent pyramids (P). The septa of Bertin are in an adult kidney. Each lobe contains a pyramid. Note the hyperechoic
highly echogenic. tissue between the two pyramids, representing septa of Bertin.
FIG. 14. Fetal lobation and scars. Sagittal scan of a kidney shows fetal
lobation (white and black arrows). An indentation (black arrow) in the
middle of the margin of a renal lobe is caused by scar. Extensive irregular
cortical defects (arrowheads) seen in the upper pole is caused by a scar or
scars. In one renal lobe, the pyramid (p) is only slightly decreased in size,
but the cortex is absent. The other pyramid (p’) is small.
FIG. 17. Milk of calcium in a renal cyst. A 33-year-old woman with hematuria. Radiograph, ultrasonogram, and CT scan were obtained elsewhere (not
shown), and a right renal stone was diagnosed. Our ultrasonograms revealed a right renal cyst with milk of calcium rather than a stone. Computed
tomography scans and radiographs were repeated thereafter. B and D. Longitudinal scans of the right kidney with the patient in the supine and prone
positions, respectively, show a cyst (arrowheads) with milk of calcium (arrows) layering in the dependent portion of the cyst. A. Unenhanced CT scan shows
a calcified lesion (arrow) similar to a stone. C. Repeat scanning at 0.5-cm intervals shows the stone is in fact a small cyst (arrowhead) with milk of calcium
(arrow) layering in the dependent portion Thin-slice CT scan was performed twice to obtain the image showing layering of milk of calcium. From: Yeh
HC, et al. Milk of calcium in renal cysts: new sonographic features. J Ultrasound Med 1992;11:195–203.
calcium cannot be diagnosed or detected on plain radio- uterine cavity and not within the endometrium. The early
graphs because of their small size. gestational sac appears empty on ultrasonography. The first
Fine-needle aspiration may show clear, yellow fluid or structure to appear within the gestational sac is usually a
dark brown, turbid fluid. It is usually difficult to aspirate the small bleb that has been considered to represent a yolk sac.
calcified material to prove milk of calcium unless the cyst If the gestational sac grows to a certain size and still shows
contains a large amount of milk of calcium and unless a no evidence of the yolk sac, it is considered to be a nonvi-
prolonged, forceful suction is applied during aspiration. able gestation or a blighted ovum.34 The critical size of
discriminatory value of the gestational sac for diagnosing a
YOLK SAC AND FETAL POLE nonviable pregnancy has been decreased from 2 cm34 on
transabdominal scanning to 0.8 cm on current endovaginal
During early pregnancy, the earliest sign of intrauterine scanners.35 In fact, in the early gestational sac, there is an
pregnancy during ultrasonography is a small, cyst-like inner cell mass that is usually too small to be seen by current
structure “within” the anterior or posterior layer of endo- ultrasound equipment. The inner cell mass subsequently
metrium. This is called the intradecidual sign,33 and the forms an early amniotic sac, the roof of which is a germ disc
cyst-like structure represents an early gestational sac. This is (bilaminate disc), i.e., the early embryo. Therefore, the first
different from a pseudogestational sac in which the cyst-like bleb that appears in a gestational sac is an amniotic sac-
structure or fluid collection represents fluid or blood in the embryo complex36 and not the yolk sac. The yolk sac at this
Ultrasound Quarterly, Vol. 17, No. 3, 2001
140 H. C. YEH
FIG. 19. Milk of calcium simulating an angiomyolipoma. A. Highly FIG. 20. Milk of calcium versus calcified cystic wall in two patients. A.
echogenic lesion (arrowhead) in the upper pole of the kidney. There is no Cyst (arrowhead) with small amount of milk of calcium (arrow) may
acoustic shadow, and the lesion is somewhat similar to an angiomyoli- simulate calcification in the cystic wall. Careful scanning may be necessary
poma. B. Because some reverberation was seen (A), milk of calcium was to show layering, reverberation echoes, and movement with gravity (not
suspected, and scanning with a perpendicular ultrasound beam with the shown) to confirm milk of calcium. B. Renal cyst (arrowhead) in another
patient in the prone position was performed, demonstrating layering of patient shows calcification (arrow) in the cystic wall casting only a weak
echogenic material, indicating milk of calcium. shadow.
to the fetus during early gestation. However, because we are lineate as two layers on ultrasonography (Fig. 24). Even if
now able to see the normal embryo or fetus, yolk sac, and one carefully delineates the double decidual sac at this
amniotic sac most of the time, we can use more precise stage, a well-formed fetus is always found in a normal preg-
terms, such as fetus, amniotic sac, yolk sac, or double bleb nancy, and the double decidual sac sign is not necessary to
instead of fetal pole, which is poorly defined. diagnose an intrauterine pregnancy. During earlier intrauter-
ine pregnancy, the gestational sac is located in a thickened
DOUBLE DECIDUAL SAC SIGN layer of decidua (the opposite layer of decidua is usually
thinner), and the thin line of the echogenic uterine cavity
It is believed that after the intradecidual sign seen in early between the two layers of decidua is usually straight or only
pregnancy, in the next stage of pregnancy, one may see a slightly displaced by the gestational sac. Therefore, two
double sac38 or a double decidual sac sign39 before the yolk layers of decidua really do not wrap around the gestational
sac or embryo can be seen. In fact, the intradecidual sign sac to form the double decidual sac sign (Figs. 25,26). Evi-
can be seen up to seventh week of pregnancy and not just dence that the double echogenic ring during early pregnancy
during the early weeks of pregnancy; although, the clinical does not represent double decidual sac include: 1) to form a
usefulness is during the early gestational stage when the double decidual sac, one should find a thin, echogenic, uter-
gestational sac appears empty. The double decidual sac sign ine cavity ring between two echogenic decidual rings to
is also useful in this empty-sac stage. A true double- indicate that this is indeed the double decidual rings divided
decidual sac sign, however, is usually not present before by the uterine cavity, i.e., one should find a third, thin,
seventh week.33,40 Two echogenic rings, one inside the echogenic ring between the two thick, echogenic rings;
other, during early pregnancy has been called the double however, this has never been documented; 2) the hy-
decidual sac sign. This is based on the assumption that each poechoic ring between the two echogenic rings should be
echogenic ring represents one layer of decidua. In fact, to determined. One speculation is that it represents fluid within
have double layers of decidua surrounding a gestational sac, the uterine cavity. Fluid in the uterine cavity during early
the gestational sac has to be large enough to markedly dis- gestation is unusual and may be abnormal. Fluid should be
place the decidua so that two layers of decidua will wrap flanked by two thin, echogenic lines (or rings) of decidual
around the gestational sac to form a double decidual sac. surface; 3) the outer echogenic ring represents the basal
This usually occurs only after approximately 8 weeks of layers of the decidual, and the inner echogenic ring repre-
gestation. By this time, the layers of decidua are markedly sents choriotrophoblastic tissue of the gestational sac. This
stretched and close to each other, and it is difficult to de- is usually evident on longitudinal scan of the uterus,
thyroiditis because of the recent discovery of a new sign, geneously hypoechoic, target-shape, large hyperechoic, or a
micronodulation.46 The sign is highly characteristic and complex mass with multiple small cystic areas. Therefore,
highly specific, with a positive predictive value of 94.7%. unlike the characteristic hypoechoic micronodules, the ul-
We have been using this sign to make initial diagnoses trasonographic features of masses caused by Hashimoto
before clinical awareness of the disease in 41 of 57 patients. thyroiditis may be entirely nonspecific, and needle biopsy
Micronodulation indicates numerous small, hypoechoic 0.2- may be necessary for a definite diagnosis.
to 0.3-cm nodules, which can occasionally be as large as 0.6 An increased risk of lymphoma in association with
cm, scattered throughout the entire thyroid gland (Fig. 27). Hashimoto thyroiditis has been reported in the literature.43
The micronodules are frequently surrounded by a thin, hy- Lymphoma tends to be hypoechoic, and three such hy-
perechoic rim that makes them highly recognizable. The poechoic masses, which I have performed biopsy on, in
hyperechoic rims are caused by fibrous strands, and the patients with this disease were caused by Hashimoto thy-
hypoechoic micronodules are caused by massive infiltration roiditis.
by an exudate of lymphocytes and some plasma cells.46 In There is also an increased risk of papillary carcinoma, of
pathology, the micronodules correspond to accentuated lob- which I have seen a few cases, and the smallest mass was
ules.47 The micronodules are usually more apparent on ob- 0.8 cm (Fig. 28). They all contained stippled calcifications
servation during actual real-time scanning than on a static caused by psammoma bodies. One should carefully evaluate
hard-copy image. During real-time scanning, as one slowly each nodule in Hashimoto thyroiditis, looking for stippled
sweeps the transducer across the thyroid gland, numerous calcifications, and if they are present, a fine-needle aspira-
micronodules appearing on consecutive images and are tion biopsy should be performed.
much more impressive than when seen on a static image.
The background echogenicity of thyroid gland in Hashi- THYROID CYST
moto thyroiditis is usually normal (50% of cases) or slightly
decreased (26% of cases), and in only 24% of the cases, it Unlike renal cysts, which are common, simple thyroid
was moderately hypoechoic. Therefore, previous descrip- cysts with an epithelial lining are rare,48 and they are not
tions of a diffusely hypoechoic thyroid gland apply only to mentioned in some popular pathology textbooks. Most cyst-
a few cases. like lesions in the thyroid gland actually have a thick wall
Although micronodules may sometimes increase in size, and represent benign colloid nodules or adenomatous nod-
they rarely grow beyond 0.6 cm. Occasionally, masses of ules that have undergone central cystic degeneration or
various sizes may be seen in a thyroid gland with Hashi- hemorrhage. The thick wall is usually isoechoic or only
moto thyroiditis, and most masses are caused by this dis- slightly hyperechoic and is frequently poorly visualized
ease, as proven by fine-needle aspiration biopsy. The (Figs. 29,30). Therefore, the thick walls are frequently not
masses may have a variety of echotextures, such as homo- delineated or recognized on ultrasonography, and the cystic
FIG. 26. Drawing depicting the formation of the double echogenic ring,
which is the so-called double decidual sac sign in a normal intrauterine
pregnancy. Left. Drawing of a sagittal scan shows a gestational sac (GS)
within the thickened posterior decidua. UC ⳱ uterine cavity line; BL ⳱
echogenic basal layer of decidua. Top right. Drawing of a transverse scan
again shows a gestational sac (GS) within the posterior decidua. A dashed
line indicates the scanning plane of the drawing in top right. Bottom
right. Drawing of oblique scan shows a double echogenic ring appearance
of the so-called double decidual sac sign. The inner echogenic ring repre-
sents the gestational sac (GS) (or choriotrophoblastic ring), and the outer
echogenic ring represents the basal layer (BL) of the decidua. The uterine
cavity line (UC) passes anterior to the gestational sac.
FIG. 27. Micronodules: variation in size in four different patients with Hashimoto thyroiditis. A. Tiny micronodules, smaller than 0.2 cm. B. Small
micronodules (0.2 cm). C. Moderate micronodules (0.25–0.35 cm). D. Large micronodules (0.3–0.4-cm). From: Yeh HC, et al. Micronodulation:
Ultrasonographic sign of Hashimoto thyroiditis. J Ultrasound Med 1996;15:813–9.
engorge to allow collateral circulation. In 24 patients with vein connecting via the superficial epigastric vein in the
portal hypertension and paraumbilical collateral circulation, subcutaneous space.
Lafortune et al.50 found on umbilicoportography that most
patients (91.7%) had a single, dilated, paraumbilical vein, HYPERECHOIC STROMA IN POLYCYSTIC
and only two patients showed two veins. In all of our 27 OVARIAN SYNDROME
patients, ultrasonography showed only a single vein.
The extrahepatic systemic connections of paraumbilical Polycystic ovarian syndrome (PCOS) is one of the most
veins have rarely been investigated in the past, and some common ovarian abnormalities in women of reproductive
authors suggest in their illustrations that the vein connects age. It is one of the most important causes of irregular
directly to the inferior vena cava at the umbilical region.53 menstruation, amenorrhea, and infertility in women. Ultra-
Based on our research of 27 patients, there are at least four sonography has an important role in the diagnosis of PCOS.
types of pathways, none through the inferior vena cava54 Hyperechoic stroma in the ovaries has been considered one
(Fig. 33). The most common pathway is through the left, of the most important ultrasonographic signs for the diag-
right, or both external iliac veins (Fig. 34) via the inferior nosis of PCOS by many researchers.55–58 In fact, I have
epigastric veins within the extraperitoneal fat space (Fig. rarely seen a truly hyperechoic stroma in patients with
35). In the second common pathway, the vein makes a sharp PCOS. With PCOS, there are always multiple, moderate-
turn upward to connect to the innominate vein in the chest size, developing follicles, usually 0.5 to 0.8 cm, and there is
via the superior epigastric vein. In the third type, the vein through transmission of ultrasound beams through the fol-
divides after exiting from the liver to connect to both the licles. This results in a hyperechoic area in the ovarian
external iliac vein inferiorly and the innominate vein supe- stroma behind the follicles. For areas not behind the fol-
riorly. The least common pathway is the greater saphenous licles, the echotexture of the stroma is similar to that of the
FIG. 29. Cystic lesion of the thyroid gland. A. Sagittal scan of right lobe
shows a lesion possibly representing a simple cyst. B. Scanned more care-
fully, an isoechoic thick wall (between [+]) is delineated. C. After aspira-
tion, a solid mass (arrowheads) with a collapsed slit-like central cystic area
is seen. Aspiration at this time gained more tissue than did aspiration of the
cystic fluid.
FIG. 30. Complex thyroid mass. A. Lesion in the thyroid gland was
initially considered a cyst (arrowheads) with internal echoes. B. On careful
scanning, a thick, solid, isoechoic wall (arrowheads) is seen, indicating that FIG. 32. Paraumbilical vein. A. Transverse scan of the epigastrium
this is a mass with central cystic degeneration. shows the falciform ligament (f) just below the liver. The round ligament
(r) is at its posterior margin, and a slightly prominent paraumbilical vein (v)
is adjacent to the round ligament. B. Drawing of the view from within the
anterior abdominal wall. f ⳱ falciform ligament; r ⳱ round ligament; v ⳱
37,38). The diaphragmatic slip will become elongated and paraumbilical vein; D ⳱ diaphragm.
can be seen obliquely across the diaphragm. The elongated
diaphragmatic slip contains multiple linear echoes, usually ABDOMINAL AORTIC ANEURSYM
up to four, caused by two layers of diaphragm (Figs. 37,38).
This feature is diagnostic for a diaphragmatic slip, and when There are some controversies and pitfalls pertaining to
this is seen, a tumor can be excluded. When multiple dia- abdominal aortic aneurysm. An abdominal aortic aneurysm
phragmatic slips are seen, one may observe scalloping of the has been frequently defined as a focal dilatation of the ab-
diaphragm during deep inspiration (Fig. 39). dominal aorta to larger than 2.966,67 or 3 cm63–65 in diam-
eter. The size of normal aorta is highly variable and can be
as small as 1.2 cm in diameter in adults (Fig. 40). It is
usually larger superiorly, especially proximal to the renal
arteries. The normal aorta gradually tapers off distally.68
Focal dilatation of 3 cm compared with an aorta of 1.2 cm
is a 150% increase in diameter, but compared with an aorta
of 2.5 cm, there is only a 20% increase in diameter. There-
fore, the size of an aneurysm may have different clinical
significance in different patients. Other authors69–71 define
the diameter of the abdominal aorta as a ratio of more than
1.5, i.e., focal dilatation of the aorta with at least a 50%
increase in diameter compared with the expected normal
diameter of the aorta. In this regard, normal arterial diam-
eters determined from selected data in the literature should
be considered.69 Given the assumption that arterial (or aor-
FIG. 31. Small cyst in the thyroid gland. Transverse scan shows a 0.2-cm
cyst (arrowhead) in the thyroid gland. This most likely represents an en- tic) diameter proximal to a dilatation is normal, increase in
larged follicle. diameter greater than 50% of the artery proximal to the
dilatation may also be considered an aneurysm.69 However, than 1.5 should be followed-up to prevent spontaneous rup-
because all aneurysms grow from small size, all small fo- ture of aneurysms. Therefore, defining an abdominal aortic
cal dilatations of the aorta should be reported. Because pa- aneurysm to be more than 3 cm in diameter or as having more
tients are usually asymptomatic before the rupture of an than 1.5 in diameter ratio is indeed not appropriate. A smaller
aneurysm, and because the mortality rate of spontaneous focal dilatation should also be included with the term “aneu-
rupture of an aortic aneurysm is high (>70%),72 patients rysm,” but at the same time, one should include diameter ratio
who have a small aneurysm with a diameter ratio smaller
Because most CT scans are performed in the axial plane delineated, unless heavy calcification is present. One should
only, an aneurysm of a tortuous aorta can be difficult to measure from outer wall to outer wall of the aneurysm.
accurately measure. An iliac artery aneurysm may even be When the wall of the aneurysm is thick, it may result in a
mistook for a large aortic aneurysm (Fig. 41). Unless a significant difference in the result of measurement if the
high-resolution, three-dimensional reconstruction is per- measurements are performed from the outer wall to inner
formed, an accurate measurement of an aortic aneurysm on wall or the inner wall to inner wall. The measurement of
a tortuous aorta with a complicated curve can be difficult on outer wall to outer wall will correlate much better with the
CT scanning. In a tortuous aorta with a complicated curve, surgical findings, and if one consistently measures in the
one part of the aorta may be in one oblique direction and same manner each time, the progressive change of an an-
another part in another oblique direction. When measuring eurysm during follow-up examinations will be more pre-
these two aneurysms, one should scan along the central axis cise, even if performed by a different ultrasonographer. Ac-
of each aneurysm and measure each aneurysm in two dif- curate measurement of the aneurysm is important. One of
ferent images. This can be performed with ultrasonography the criteria for surgical indication for abdominal aortic an-
(Fig. 42).75 Double aneurysms adjacent to each other may eurysm is an increase in diameter of 1 cm over the course of
sometimes be difficult to recognized on the axial CT scan 1 year. If follow-up examination is performed within 6
(Fig. 42). A small aneurysm is also easily missed on CT months or less, an increase in diameter of 0.5 cm will be
scan (Fig. 43). clinically highly significant. If intraobserver or interob-
How should the aneurysm be measured? Some people server error is larger than 0.3 cm, then, when an increase in
measure from the outer wall to inner wall, from the inner diameter of 0.6 cm is encountered on follow-up examina-
wall to inner wall,75 or with no criteria at all. Because tion, the clinical significance of this finding may be uncer-
gray-scale ultrasound has been greatly improved, the actual tain. This is because this may actually mean a difference of
thickness of the wall of an aortic aneurysm can be clearly only 0.3 cm, or maybe up to 0.9 cm, which is highly sig-
nificant. In my experience, when the aneurysmal wall is called “fetal lobation.” To differentiate this entity from scars
clearly delineated on both sides and the measurement is and tumors, one should carefully examine each renal lobe
performed on proper sagittal or coronal plane, the intraob- that consists of a pyramid overlaid by a “bump” of cortex on
server error is usually less than 0.1 cm. the renal contour.
Milk of calcium in a renal cyst is common, contrary to the
CONCLUSION belief that it is rare. Ultrasonography is much better than CT
for diagnosing milk of calcium, and even a tiny 0.2-cm
The term “column of Bertin” is a misnomer, and “septum lesion can be detected. On CT, milk of calcium can be
of Bertin” (or “cloisonné of Bertin”) is the proper term. mistaken for a stone or tumor. On ultrasonograph, however,
Although septum of Bertin has the same histologic structure milk of calcium sometimes may mimic a stone, angiomyo-
as renal cortex, it is usually much more echogenic than renal lipoma, or cyst with calcified wall. A small bleb that first
cortex because of the difference in orientation of the lobules appears in the gestational sac (single-bleb sign) represents
and vessels. This is caused by the anisotropic effect. an embryo–amniotic sac complex and not a yolk sac.
The terms “hypertrophic column of Bertin” and “lobar The double decidual sac sign has been considered one of
dysmorphism” should be called “junctional parenchyma,” the most important signs of an intrauterine pregnancy before
which represents the unresorbed renal parenchyma at the the amniotic sac, yolk sac, or embryo can be seen. In fact,
junction of two subkidneys that fuse to form a normal kid- the double decidual sac sign is formed only after approxi-
ney. The renal cortex, pyramid, and septa of Bertin within mately the eighth week of pregnancy and is difficult to
the junctional parenchyma are all normal, and there is noth- delineate. Even if it is delineated, a live fetus should be
ing hypertrophic or displaced. When the elements of the seen, and so there is no need for the double decidual sign to
junctional parenchyma are delineated by ultrasonography, diagnose an intrauterine pregnancy. The double echogenic
the diagnosis is certain and tumor can be excluded. rings during early pregnancy do not represent the double
A true hypertrophic septum (or septa) of Bertin is usually decidual sign.
hyperechoic, pear-shape, and symmetrically flanked by the Micronodulation is a highly specific and useful sign for
pyramids. It is usually located in the anterior aspect of the Hashimoto thyroiditis. Because of the increased incidence
midportion of the kidney, whereas a junctional parenchyma of papillary carcinoma in Hashimoto thyroiditis, one should
is usually located in the lateral aspect of the kidney at the carefully look for stippled calcifications in the nodules.
junction between the upper and middle thirds of the kidney. Recanalization of the umbilical vein rarely occurs. The
The term “fetal lobulation” should be more properly collateral vein seen is usually a dilated paraumbilical vein
that may drain through the inferior epigastric–external iliac 18. Palma LD, Bazzocchi M, Cressa C, et al. Radiological anatomy of the
kidney revisited. Br J Radiol 1990;63:680–90.
veins or the superior epigastric–internal thoracic veins. 19. Maklad NF, Chuang VP, Doust BD, et al. Ultrasonic characterization
Hyperechoic stroma is not a common or important sign in of solid renal lesions: echographic, angiographic, and pathologic cor-
polycystic ovarian syndrome. The hyperechogenicity of the relation. Radiology 1977;123:733–9.
stroma is usually caused by increased through transmission 20. Yeh HC, Halton KP, Shapiro RS, et al. Junctional parenchyma: revised
definition of hypertrophic column of Bertin. Radiology 1992;185:
caused by the presence of multiple developing follicles. 725–32.
Bilateral, multiple, developing follicles are the most impor- 21. Fine H, Keen EN. The arteries of the human kidney. J Anat 1966;100:
tant diagnostic feature for polycystic ovarian syndrome. 881–94.
22. Hoffer FA, Hanabergh AM, Teele RL. Interrenicular junction: a mimic
Diaphragmatic slips may simulate liver masses. Scanning of renal scarring on normal pediatric sonograms. AJR Am J Roentgenol
along the long axis of the slip shows a band-like structure 1985;145:1075–8.
with multiple linear echoes. This is the diagnostic feature. 23. Rubin JM, Carson PL, Meyer CR. Anisotropic ultrasonic backscatter
from the renal cortex. Ultrasound Med Biol 1988;14:507–11.
Defining an abdominal aortic aneurysm as having a di- 24. Patriquin H, Lefaivre JF, Lafortune M, et al. Fetal lobation, an
ameter greater than 3 cm or with a diameter ratio of greater anatomo-ultrasonographic correlation. J Ultrasound Med 1990;9:
than 1.5 will prevent many patients who have smaller an- 191–7.
25. Widder DJ, Newhouse JH. The sonographic appearance of milk of
eurysms from needing follow-up examinations. Measure- calcium in renal calyceal diverticuli. J Clin Ultrasound 1982;10:488.
ment of an aneurysm should be performed on a longitudinal 26. Walker WH, Pearson RE, Johnson NR. Milk of calcium renal stone:
scan along the long axis of the aneurysm. When the aorta is Case report. J Urol 1960;84:517.
markedly tortuous with multiple aneurysms, each aneurysm 27. Becker JA, Staiano S. Milk of calcium in a renal cyst: A sonolucent
mass effect. J Clin Ultrasound 1975;3:135.
should be measured along its own long axis. 28. Diakoumakis E, Vieux U, Seife B, et al. Case report: Ultrasonographic
features of “milk of calcium” in kidney. Mt Sinai J Med 1985;52:656.
Acknowledgment: The author thanks Ms. Gwen Hanley for her 29. Tey PH, Ahmed A, Chan KF. Case report: milk of calcium in kidney
excellent secretarial work. after cyst puncture. Mt Sinai J Med 1985;52:659.
30. Dyer R, Montgomery J, Thiele A, et al. Right upper quadrant renal
milk of calcium mimicking limy bile. J Clin Ultrasound 1987;15:140.
REFERENCES 31. Yeh HC, Mitty HA, Halton K, et al. Milk of calcium in renal cysts:
new sonographic features. J Ultrasound Med 1992;11:195–203.
1. Hodson J. The lobar structure of the kidney. Br J Urol 1972;44: 32. Vandeursen H, Baert L. An intrarenal opacity resisting extracorporeal
246–61. shock wave lithotripsy. J Urol 1990;144:961.
2. Mahony BS, Jeffrey RB, Laing F. Septa of Bertin: a sonographic 33. Yeh HC, Goodman JD, Carr L, et al. Intradecidual sign: an US crite-
pseudotumor. J Clin Ultrasound 1983;11:317–9. rion of early intrauterine pregnancy. Radiology 1986;161:463–7.
3. Netter F. Kidneys, ureters and urinary bladder. In: Shapter RK, Yon- 34. Bernard KG, Cooperberg PL. Sonographic differentiation between
kman FF, eds. The Ciba Collection of Medical Illustration. Summit, blighted ovum and early viable pregnancy. AJR Am J Roentgenol
NJ: Ciba Pharmaceutical, 1979;6:5. 1985;144:597.
4. Wolfman NT, Bechtold RE, Watson NE. Hypertrophic column of 35. Levi CS, Lyons EA, Lindsay DJ. Early diagnosis of nonviable preg-
Bertin. In: Resnick ML, Rifkin MD, eds. Ultrasonography of the nancy with endovaginal ultrasound. Radiology 1988;167:383–5.
Urinary Tract, 3rd ed. Baltimore: Williams & Wilkins, 1991:109–51. 36. Yeh HC, Rabinowitz JG. Endovaginal ultrasonographic measurement
5. Lafortune M, Constantin A, Breton G, et al. Sonography of the hy- of embryonic size (Letter). J Ultrasound Med 1995;14:97–100.
pertrophied column of Bertin. AJR Am J Roentgenol 1986;146:53–6. 37. Horrow SR. Yolk sac sign: sonographic appearance of the fetal yolk
6. Leekman RN, Martizinger MA, Brunelle M, et al. The sonography of sac in missed abortion. J Ultrasound Med 1986;5:435–8.
renal columnar hypertrophy. J Clin Ultrasound 1983;11:491–4. 38. Bradley WG, Fishe CE, Filly RA. The double sac sign of early intra-
7. Charghi A, Dessureault P, Drouin G, et al. Malposition of a renal lobe uterine pregnancy: use in exclusion of ectopic pregnancy. Radiology
(lobar dysmorphism): a condition simulating renal tumor. J Urol 1971; 1982;143:223–6.
105:326–9.
39. Nyberg DA, Laing FC, Filly RA, et al. Ultrasonographic differentia-
8. Dacie JE. The “central lucency” sign of lobar dysmorphism (pseudo-
tion of the gestational sac of early intrauterine pregnancy from pseu-
tumor of the kidney). Br J Radiol 1976;49:39–42.
dogestational sac of ectopic pregnancy. Radiology 1983;146:755–9.
9. Felson B, Moskowitz M. Renal pseudotumors: the segmented nodule
and other lumps, bumps and dromedary humps. AJR Am J Roentgenol 40. Yeh HC. Efficacy of the intradecidual sign and fallacy of the double
1969;107:720–9. decidual sac sign in the diagnosis of early intrauterine pregnancy.
10. Lopez FA. Renal pseudotumors. AJR Am J Roentgenol 1972;129: Radiology 1999;210:579–82.
172–84. 41. Fates MC, Laing FC. Sonographic evaluation of ectopic pregnancy: an
11. Popky GL, Bogash M, Pollack H, et al. Focal cortical hyperplasia. J update. AJR Am J Roentgenol 1995;165:251–9.
Urol 1969;102:657–60. 42. Williamson MR, Rosenberg RD. Computed tomography and ultra-
12. Hodson CJ, Mariani S. Large cloisons. AJR Am J Roentgenol 1982; sound of the thyroid and parathyroid glands. In: Eisenberg B, ed.
139:327–32. Imaging of the Thyroid and Parathyroid Glands: A Practical Guide.
13. King MC, Friedenberg RM, Tena LB. Normal renal parenchyma simu- New York: Churchill Livingstone, 1991:111.
lating tumor. Radiology 1968;91:217–22. 43. Gooding GAW. Sonography of the thyroid and parathyroid. Radiol
14. Hartman GW, Hodson CJ. The duplex kidney and related abnormali- Clin North Am 1993;31:967.
ties. Clin Radiol 1969;20:387–400. 44. Nordmeye JP, Shafeh A, Heckmann C. Thyroid sonograph in autoim-
15. Thornbury JR, McCormick TL, Silver TM. Anatomic/radiologic clas- mune thyroiditis: A prospective study on 123 patients. Acta Endocri-
sification of renal cortical nodule. AJR Am J Roentgenol 1980;134: nol 1990;122:391.
1–7. 45. James EM, Charboneau JW, Hay ID. The thyroid. In: Rumack CM,
16. Meaney TF. Errors in angiographic diagnosis of renal masses. Radi- Wilson SR, Charboneau JW, eds. Diagnostic Ultrasound. St. Louis:
ology 1969;93:361–6. Mosby-Year Book, 1991:507.
17. Flynn VJ, Gittes RF. Benign cortical rest: “a pseudotumor” of the 46. Yeh HC, Futterweit W, Gilbert P. Micronodulation: Ultrasonographic
kidney. J Urol 1972;108:54–7. sign of Hashimoto thyroiditis. J Ultrasound Med 1996;15:813–9.
47. Li Volsi. Surgical Pathology of the Thyroid. Philadelphia: WB Saun- a sonographic sign of diaphragmatic disease. J Clin Ultrasound 1982;
ders, 1990:68. 10:42–5.
48. de los Santos E, Keyhani-Rofagha S, Cunningham JJ, et al. Cystic 63. Pedersen OM, Vik-MO H, Trippestad A. Diagnosis of small infrarenal
thyroid nodules. Arch Intern Med 1990;150:1422–7. aortic aneurysms by ultrasonography. Int Angiol 1996;15(4):328–34.
49. Hammer M, Wortsman J, Folse R. Cancer in cystic lesions of the 64. Kanagasabay R, Garaj H, Pointon L, et al. Co-morbility in patients
thyroid. Arch Surg 1982;117:1020–3. with abdominal aortic aneurysms. J Med Screen 1996;3(4):208–10.
50. Lafortune M, Constantin A, Breton G, et al. The recanalized vein in 65. Gooding GAW. The abdominal great vessels. In: Rumack CM, Wilson
portal hypertension: a myth. AJR Am J Roentgenol 1985;144:549–53. SR, Charboneau JW, eds. DiagnosticUltrasound. Chicago: Mosby-
51. Saddekni S, Hutchinson DE, Cooperberg PL. The sonographic patent Year Book. 1991:335–51.
umbilical vein in portal hypertension. Radiology 1982;145:441–3. 66. Lindholt JS, Fasting H, Henneberg EW, et al. Preliminary results of
52. Martin BF, Tudor RG. The umbilical and paraumbilical veins of man. screening for abdominal aortic aneurysm in the county of Vibort.
J Anat 1980;130:305–22. Ugeskr Laeger 1997;159(13):1920–3.
53. Subramanyam BR, Balthazar EJ, Madamba MR, et al. Sonography of 67. Simoni G, Gianotti A, Andia A, et al. Screening study of abdominal
portosystemic venous collaterals in portal hypertension. Radiology aortic aneurysm in a general population: lipid parameters. Cardiovasc
1983;146:161–6. Surg 1996;4(4):445–8.
54. Yeh HC, Stancato-Pasik A, Ramos R, et al. Paraumbilical venous 68. Steinberg CR, Archer M, Steinberg I. Measurement of the abdominal
collateral circulations: color Doppler ultrasound features. J Clin Ul- aorta after intravenous aortography in health and arteriosclerotic pe-
trasound 1996;24:359–66. ripheral vascular disease. AJR Am J Roentgenol 1965;95:703–8.
55. Battaglia C, Regnani G, Antin PG, et al. Polycystic ovary syndrome: 69. Johnston KW, Rutherford RB, Tilson MD, et al. Suggested standards
a new ultrasonographic and color Doppler pattern. Gynecol Endocrinol for reporting on arterial aneurysms. J Vasc Surg 191;13:452–8.
2000;14:417–24. 70. Hollier LH, Wisselink W. Abdominal aortic aneurysm. In: Haimovici
56. Pache TD, Wladimiroff JW, Hop WCJ. How to discriminate between H, Ascer E, Standness DE, et al., eds. Haimovici’s Vascular Surgery.
normal and polycystic ovaries: transvaginal US study. Radiology Cambridge, Massachusetts: Blackwell Science, 1998:797–827.
1992;183:421–3. 71. Goldstone J. Aneurysm of the aorta and iliac artery. In: Moore WS, ed.
57. Saxton DW, Farguhar CM, Beard TR, et al. Accuracy of ultrasound Vascular Surgery, 5th ed. Philadelphia: WB Saunders, 1998:435–55.
measurements of female pelvic organ. Br J Obstet Gynecol 1990;97: 72. Pearce WH, Salyapongse AN, Fitzgerald SW, et al. Computerized
695–9. tomographic scanning and vascular disorders. In: Callow AD, Ernst
58. Adams J, Polson DW, Abdulwahid N, et al. Multifollicular ovaries: CB, eds. Vascular Surgery: Theory and Practice. Stamford, CT:
clinical and endocrine features and response to pulsatile gonadotropin Appleton & Lange, 1995:394.
releasing hormone. Lancet 1985;2:1375–8. 73. Cook TA, Gallard RB. A prospective study to define the optimum
59. Yeh HC, Futterweit W, Thornton JC. Polycystic ovarian disease: US rescreening interval for small abdominal aortic aneurysm. Cardiovasc
features in 104 patients. Radiology 1987;163:111–16. Surg 1996;4(4):441–4.
60. Yeh HC, Halton KP, Gray CE. Anatomic variations and abnormalities 74. Chang JB, Stein TA, Liu JP, et al. Risk factors associated with rapid
in the diaphragm seen with US. Radiographics 1990;10:1019–30. growth of small abdominal aortic aneurysms. Surgery 1997;121(2):
61. Auh YH, Rubenstein WA, Zirinsky K, et al. Accessory tissues of the 117–22.
liver: CT and sonographic appearance. AJR Am J Roentgenol 1984; 75. Lanne T, Sandgren T, Mangell P, et al. Improved reliability of ultra-
143:565–72. sonic surveillance of abdominal aortic aneurysm. Eur J Vasc Endovasc
62. Worthen JH, Worthen WF II. Disruption of the diaphragmatic echoes: Surg 1997;13(2):149–53.