Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly

Diphallus is a rare anomaly and its association with urethral duplication is extremely rare. Numerous associated genitourinary and gastrointestinal anomalies have been reported with this condition. Challenges in the management are incorporation of the glans and the dominant urethra during reconstruc...

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Detalles Bibliográficos
Autores principales: Aihole, Jayalaxmi S., Babu, Narendra, Shankar, Gauri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626927/
https://www.ncbi.nlm.nih.gov/pubmed/26604454
http://dx.doi.org/10.4103/0970-1591.166458
Descripción
Sumario:Diphallus is a rare anomaly and its association with urethral duplication is extremely rare. Numerous associated genitourinary and gastrointestinal anomalies have been reported with this condition. Challenges in the management are incorporation of the glans and the dominant urethra during reconstruction. We report the successful management of a case of glandular diphallus with complete urethral duplication retaining the dorsal urethra.

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