Misdiagnosis of congenital posterior urethroperineal fistula and comparison with urethral duplications and rectourethral fistula
Congenital posterior urethroperineal fistula (CUPF) is a urothelium-lined tract between the posterior urethra and perineum. This condition is rare and has been proposed to be a urethral duplication variant. A case of CUPF that was misdiagnosed and surgically treated as a rectourethral fistula is presented. The clinical presentation, diagnosis, and treatment of CUPF are discussed and compared with those of Y-type urethral duplications and H-type rectourethral fistulas.
Source: Urology - Category: Urology & Nephrology Authors: Julie W Cheng, Jennifer J Ahn, Mark P Cain, Jamie E Anderson, Caitlin A Smith, Samuel E Rice-Townsend Source Type: research
More News: Urology & Nephrology