Abstract
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.
Original language | English (US) |
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Pages (from-to) | 193-196 |
Number of pages | 4 |
Journal | Urology |
Volume | 158 |
DOIs | |
State | Published - Dec 2021 |
Externally published | Yes |
Keywords
- congenital abnormalities
- perineum
- urethra
- urinary fistula
- urinary tract
ASJC Scopus subject areas
- Urology