The Fetal Urinoma Revisited he fetal urinoma is quite rare and presents as an encapsulated fluid collection caused by the extravasation of urine into the perirenal spaces. Fetal urinomas are strongly associated with obstructive uropathy usually secondary to posterior urethral valves or ureteropelvic junction obstruction. 1,2 Urinomas have been associated with minimal or no function in the affected kidney. 3,4 A recent meta-analysis reported the probability of an ipsilateral nonfunctioning kidney to be as high as 80%. 5 However, this point remains controversial, and there are contradicting and limited data in the literature. 6 Preservation of renal function is reportedly better in lower urinary tract obstruction than in upper urinary tract obstruction. Additional factors at play in predicting renal function include age at presentation and underlying pathologic conditions. 7
Materials and MethodsWe performed a retrospective review of our institution's imaging database, which identified 25 cases of fetal urinomas imaged prenatally at the University of California San Francisco Fetal Treatment Center between 2000 and 2011. Fetal sonograms were reviewed by all authors for specific features, including sex, the side of the urinoma, the location of the urinoma with respect to the kidney, size, and etiology. When available, the prenatal imaging findings were correlated with interventions and outcomes. The fetal urinoma is a rare but important diagnosis, as it indicates substantial underlying obstruction with implications for the functionality of the affected kidney. This case series describes a single center's experience with the diagnosis and management of fetal urinomas. All 25 cases were diagnosed or referred to our medical center over an 11-year period. Most cases were secondary to either posterior urethral valves or ureteropelvic junction obstruction. Fetal interventions, including percutaneous drainage of the urinoma and cystoscopic alleviation of bladder outlet obstruction, were performed in 4 cases.