A rare case of adult diphallus with anorectal malformation
We present the case of a 24 year old man who presented with acute urinary retention and found to have diphallus with vertical duplication of penis. Superior phallus was well developed without any urethral meatus whereas inferior phallus was rudimentary but with patent urethra. History of erection wa...
Main Authors: | Shailesh C Sahay, P N Dogra, Pramod K Rai |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2012-01-01
|
Series: | Indian Journal of Urology |
Subjects: | |
Online Access: | http://www.indianjurol.com/article.asp?issn=0970-1591;year=2012;volume=28;issue=3;spage=357;epage=358;aulast=Sahay |
Similar Items
-
Diphallus: A Rare Urological Anomaly- What to Do Next? Case Report and Literature Review
by: Halil Ibrahim Ivelik, et al.
Published: (2023-05-01) -
Covered exstrophy with anorectal malformation and vaginal duplication
by: Jitendra K Singh, et al.
Published: (2011-01-01) -
Covered exstrophy with anorectal malformation and vaginal duplication
by: Bawa Monika, et al.
Published: (2011-01-01) -
Complete duplication of the urinary bladder: An extremely rare congenital anomaly
by: Vishal Gajbhiye, et al.
Published: (2015-01-01) -
Gastric Duplication Cyst Associated with Esophageal Atresia and Anorectal Malformations: A Rare Association
by: Rajat Piplani, et al.
Published: (2018-07-01)