Diphallia with Associated Anomalies: A Case Report and Literature Review

Diphallia or penile duplication is an extremely rare congenital anomaly. It occurs once in every 5.5 million live births. The extent of penile duplication and the number of associated anomalies vary greatly, ranging from a double glans from a penis with no associated anomaly up to complete penile du...

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Autores principales: Tirtayasa, Pande Made Wisnu, Prasetyo, Robertus Bebet, Rodjani, Arry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870645/
https://www.ncbi.nlm.nih.gov/pubmed/24383036
http://dx.doi.org/10.1155/2013/192960
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author Tirtayasa, Pande Made Wisnu
Prasetyo, Robertus Bebet
Rodjani, Arry
author_facet Tirtayasa, Pande Made Wisnu
Prasetyo, Robertus Bebet
Rodjani, Arry
author_sort Tirtayasa, Pande Made Wisnu
collection PubMed
description Diphallia or penile duplication is an extremely rare congenital anomaly. It occurs once in every 5.5 million live births. The extent of penile duplication and the number of associated anomalies vary greatly, ranging from a double glans from a penis with no associated anomaly up to complete penile duplication associated with multiple anomalies. Here, we report a 12-year-old boy with complete bifid diphallia associated with bifid scrotum, epispadia, and pubic symphysis diastasis along with a review of the articles pertaining to this anomaly.
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spelling pubmed-38706452014-01-01 Diphallia with Associated Anomalies: A Case Report and Literature Review Tirtayasa, Pande Made Wisnu Prasetyo, Robertus Bebet Rodjani, Arry Case Rep Urol Case Report Diphallia or penile duplication is an extremely rare congenital anomaly. It occurs once in every 5.5 million live births. The extent of penile duplication and the number of associated anomalies vary greatly, ranging from a double glans from a penis with no associated anomaly up to complete penile duplication associated with multiple anomalies. Here, we report a 12-year-old boy with complete bifid diphallia associated with bifid scrotum, epispadia, and pubic symphysis diastasis along with a review of the articles pertaining to this anomaly. Hindawi Publishing Corporation 2013 2013-12-08 /pmc/articles/PMC3870645/ /pubmed/24383036 http://dx.doi.org/10.1155/2013/192960 Text en Copyright © 2013 Pande Made Wisnu Tirtayasa et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tirtayasa, Pande Made Wisnu
Prasetyo, Robertus Bebet
Rodjani, Arry
Diphallia with Associated Anomalies: A Case Report and Literature Review
title Diphallia with Associated Anomalies: A Case Report and Literature Review
title_full Diphallia with Associated Anomalies: A Case Report and Literature Review
title_fullStr Diphallia with Associated Anomalies: A Case Report and Literature Review
title_full_unstemmed Diphallia with Associated Anomalies: A Case Report and Literature Review
title_short Diphallia with Associated Anomalies: A Case Report and Literature Review
title_sort diphallia with associated anomalies: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870645/
https://www.ncbi.nlm.nih.gov/pubmed/24383036
http://dx.doi.org/10.1155/2013/192960
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