Literature DB >> 26610674

A Case of Bifid Phallus and Bladder Neck Incompetence: Is This a Variant of Epispadias or Hypospadias?

Fumi Matsumoto1, Yoshiyuki Onitake2, Futoshi Matsui2, Kenji Shimada2.   

Abstract

Diphallia or duplication of the penis is an extremely rare congenital anomaly. Based on the presence of one or two corpora cavernosa in each of the penises, diphallia is classified into two major groups: bifid phallus and true diphallia. Because true diphallia associated with various anomalies is dominant in published studies, little is known about bifid phallus or isolated cases. Here we present a 9-month-old boy with an isolated bifid phallus. After successful reconstruction of the penis and urethra, urinary incontinence became apparent. To the best of our knowledge, this is the first case of complete bifid phallus associated with bladder neck incompetence.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2015        PMID: 26610674     DOI: 10.1016/j.urology.2015.11.007

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  2 in total

Review 1.  Diphallia: literature review and proposed surgical classification system.

Authors:  Dylan John Kendrick; Roy Mark Kimble
Journal:  ANZ J Surg       Date:  2022-06-09       Impact factor: 2.025

2.  A Rare Case of Human Diphallia Associated with Hypospadias.

Authors:  Andrey Frolov; Yun Tan; Mohammed Waheed-Uz-Zaman Rana; John R Martin
Journal:  Case Rep Urol       Date:  2018-06-13
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.