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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507414/ https://www.ncbi.nlm.nih.gov/pubmed/23204673 http://dx.doi.org/10.4103/0970-1591.102729 |
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author | Sahay, Shailesh C. Dogra, P. N. Rai, Pramod K. |
author_facet | Sahay, Shailesh C. Dogra, P. N. Rai, Pramod K. |
author_sort | Sahay, Shailesh C. |
collection | PubMed |
description | 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 was present in superior phallus only whereas patient was voiding urine from inferior phallus. It was associated with anorectal malformation and bilateral pelvic ectopic kidneys. Patient was managed by suprapubic catheter placement and planned for penile and urethral reconstructive surgery. Diphallus very rarely present in adulthood and vertical duplication is very unusual. |
format | Online Article Text |
id | pubmed-3507414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35074142012-11-30 A rare case of adult diphallus with anorectal malformation Sahay, Shailesh C. Dogra, P. N. Rai, Pramod K. Indian J Urol Uroradiology 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 was present in superior phallus only whereas patient was voiding urine from inferior phallus. It was associated with anorectal malformation and bilateral pelvic ectopic kidneys. Patient was managed by suprapubic catheter placement and planned for penile and urethral reconstructive surgery. Diphallus very rarely present in adulthood and vertical duplication is very unusual. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3507414/ /pubmed/23204673 http://dx.doi.org/10.4103/0970-1591.102729 Text en Copyright: © Indian Journal of Urology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Uroradiology Sahay, Shailesh C. Dogra, P. N. Rai, Pramod K. A rare case of adult diphallus with anorectal malformation |
title | A rare case of adult diphallus with anorectal malformation |
title_full | A rare case of adult diphallus with anorectal malformation |
title_fullStr | A rare case of adult diphallus with anorectal malformation |
title_full_unstemmed | A rare case of adult diphallus with anorectal malformation |
title_short | A rare case of adult diphallus with anorectal malformation |
title_sort | rare case of adult diphallus with anorectal malformation |
topic | Uroradiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507414/ https://www.ncbi.nlm.nih.gov/pubmed/23204673 http://dx.doi.org/10.4103/0970-1591.102729 |
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