Congenital urethroperineal fistula with scrotal localization: A case report

Abstract

Mahamoud Omid Ali Ada, Hellé Moustapha, Oumarou Habou, Amadou Soumana, Halidou Maazou, Habibou Abarchi

A congenital urethroperineal fistula (CUPF) is a rare malformation that can be considered an unusual form of urethral duplication. A 3-year-old boy presented with an orifice in the middle of his scrotum through which urinary leakage was observed during micturition. Retrograde and voiding urethrocystograms showed a fistula tract extending from the prostatic urethra to his perineum. He was successfully treated with resection of the fistula performed via a perineal approach. No clinical sign and radiological evidence of disease were observed during his 4-month postoperative follow-up. Accurately distinguishing CUPF from a similar form of urethral duplication (type II A2-Y urethral duplication) is important for definitive treatment.

PDF

Share this article

Get the App

paper.io

agar io

wowcappadocia.com cappadocia tours
cappadocia-hotels.com cappadocia hotels
caruscappadocia.com cappadocia hotel
brothersballoon.com cappadocia balloon
balloon-rides.net cappadocia balloon flights

wormax io