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Molecular Biophysics
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- Pediatric Case Reports
Misdiagnosis of Congenital Posterior Urethroperineal Fistula and Comparison With Urethral Duplications and Rectourethral Fistula
UrologyVol. 158p193–196Published online: October 1, 2021- Julie W. Cheng
- Jennifer J. Ahn
- Mark P. Cain
- Jamie E. Anderson
- Caitlin A. Smith
- Samuel E. Rice-Townsend
Cited in Scopus: 1Congenital 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.