Diphallia with Associated Anomalies: A Case Report and Literature Review-Reference-Cited by-同舟云学术

Diphallia with Associated Anomalies: A Case Report and Literature Review

Published:2013 Issue: Volume:2013 Page:1-4
ISSN:2090-696X
Container-title:Case Reports in Urology
language:en
Short-container-title:Case Reports in Urology

Author:

Tirtayasa Pande Made Wisnu¹^ORCID,Prasetyo Robertus Bebet²,Rodjani Arry¹

Affiliation:

1. Department of Urology, Cipto Mangunkusumo Hospital, Jl. Diponegoro No. 71, Jakarta 10430, Indonesia

2. Department of Surgery, Division of Urology, Gatot Subroto Army Hospital, Jakarta 10410, Indonesia

Abstract

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.

Publisher

Hindawi Limited

Subject

General Medicine

Link

http://downloads.hindawi.com/journals/criu/2013/192960.pdf

Reference24 articles.

1. Successful surgical correction of true diphallia, scrotal duplication, and associated hypospadias

2. Diphallus with ectopic bowel segment: a case report

3. Clinical and embryologic aspects of penile duplication and associated anomalies

4. Complete diphallia

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