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Case Reports in Urology
Volume 2013 (2013), Article ID 192960, 4 pages
http://dx.doi.org/10.1155/2013/192960
Case Report

Diphallia with Associated Anomalies: A Case Report and Literature Review

1Department of Urology, Cipto Mangunkusumo Hospital, Jl. Diponegoro No. 71, Jakarta 10430, Indonesia
2Department of Surgery, Division of Urology, Gatot Subroto Army Hospital, Jakarta 10410, Indonesia

Received 30 July 2013; Accepted 11 November 2013

Academic Editors: S.-S. Chen, P. H. Chiang, A. Goel, A. Greenstein, S. K. Hong, and A. A. Rodrigues

Copyright © 2013 Pande Made Wisnu Tirtayasa et al. 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.

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.