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Urinoma
A urinoma is a fluid collection formed by extravasated urine encapsulated in the perirenal
fascia.
include:
Sonographic Diagnosis:
Fetal urinoma can easily be diagnosed on prenatal ultrasound ( Figure 18-33 ). The
differential diagnosis includes hydronephrosis, cystic renal disease, duplication of the
intrarenal collecting system, cystic renal tumour, cystic lymphangioma, mesenteric cyst and
enteric duplication cyst.
FIGURE 18-33
Fetal urinoma (block arrow) in a fetus with obstructive uropathy due to posterior
urethral valves (line arrow points to massively distended fetal bladder).
(Courtesy of Dr Anne Marie Coady.)
In about 80% of the cases the renal function of the affected kidney is impaired. A change in
size of the urinoma, the use of in-utero puncture and the existence of normal or hyperechoic
renal parenchyma appear to have no influence on the prognosis, either positive or negative.
In-utero puncture only appears to be justified in cases where the urinoma has a mass effect on
adjacent major structures (especially the contralateral kidney), or in the case of probable
dystocia.
Pathology
parapelvic cysts: originate from the adjacent parenchyma and protrude into the renal
sinus
peripelvic cyst: originate within the sinus itself and have a lymphatic origin
Parapelvic cysts
These are simple renal cysts that plunge into the renal sinus from the adjacent renal
parenchyma. They are usually single or few and resemble simple renal cortical cyst in
morphology. A parapelvic cyst at times may cause compression of the pelvicalyceal system
resulting into hydronephrosis.
Peripelvic cysts
These are frequently bilateral. They appear as water attenuation cysts closely abutting the
pelvis and infundibula, rarely cause functional renal derangement by compression. When
followed up they remain unchanged in size. They may be confused with hydronephrosis on
NECT and USG, but on CECT the differentiation is obvious.