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CHAPTER 39 The Fetal Urogenital Tract 1353

FIG. 39.22 Congenital Mesoblastic Nephroma. Longitudinal scan

of a 35-week fetus shows a large, heterogeneous solid mass (calipers)

replacing most of the right kidney, except for the upper pole (arrow).

FIG. 39.23 Normal Adrenal Gland. Longitudinal scan of a 31-week

fetus demonstrates the Y- or V-shaped adrenal gland (arrow) at the

superior border of the kidney (K).

Mesoblastic nephroma is usually seen as a moderately echogenic,

solid mass completely replacing the kidney or localized to part

of the kidney 111 (Fig. 39.22). he mass may demonstrate increased

vascularity and cystic components. Polyhydramnios is a frequent

association 110,112 and may lead to preterm labor and preterm

birth. Perinatal complications are likely, including acute fetal

distress, neonatal hypertension, and hypercalcemia. 110 Other

reported fetal renal tumors include an intrarenal neuroblastoma,

a tumor much more frequently associated with the adrenal

gland. 113

Adrenal Mass

At the end of the irst trimester, the normal adrenal glands appear

as pyramid-shaped hypoechoic structures at the superior aspect

of the kidneys. hey are quite prominent, approximately half

the size of the kidney. he size of the adrenal gland increases

with gestation, but relatively less than the kidney. During the

second and third trimesters, corticomedullary diferentiation is

apparent, with a hyperechoic medulla and a hypoechoic cortex.

On longitudinal sonogram, the adrenals are seen as V- or

Y-shaped structures superior to the kidneys (Fig. 39.23).

Abnormalities of the adrenal gland include hemorrhage, cyst,

hypertrophy, and tumor. he diferential diagnosis for fetal

suprarenal masses includes those of adrenal origin (including

adrenal neuroblastoma, adrenal hemorrhage, adrenal cyst, and

rarely adrenal cortical adenoma or carcinoma) and those of

extraadrenal origin (including those of renal origin [such as

mesoblastic nephroma, duplication anomaly with hydronephrosis,

upper-pole cystic dysplasia, urinoma], intraabdominal

pulmonary sequestration, enteric duplication cysts, splenic

cysts, and lymphangioma) (Table 39.3). 114-116

Neuroblastoma may occur anywhere along the sympathetic

chain, but 90% are located in the adrenal gland. he prenatal

sonographic appearance is variable and ranges from a complex

cystic mass with thick septations (the most common presentation),

to a uniformly echogenic solid mass (Fig. 39.24), to rarely

calciied. 116-118 Importantly, a complex cystic neuroblastoma is

FIG. 39.24 Adrenal Neuroblastoma. Longitudinal scan shows a

large echogenic solid mass (calipers) adjacent to the upper pole of the

left kidney (K). (Courtesy of John R Mernagh, MD, McMaster University

Medical Center, Hamilton, Ontario.)

TABLE 39.3 Suprarenal Masses

Adrenal Origin

Neuroblastoma

Hemorrhage

Cyst

Adenoma or carcinoma

Nonadrenal Origin

Renal origin: tumor (e.g.,

mesoblastic nephroma),

duplication anomaly,

upper-pole cystic

dysplasia, urinoma

Intraabdominal pulmonary

sequestration

Enteric duplication cyst

Splenic cyst

Lymphangioma

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