Congenital Urethrocutaneous Fistula: An Interesting Case.

A congenital urethrocutaneous fistula is a rare anomaly which was first described in 1962 by Gupta. Clinically, children present when their guardian is alarmed by either frequent urinary dribbling or unusual stream when they pass urine. This congenital anomaly can present in isolation or be accompan...

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Bibliographic Details
Main Authors: AI, Roger (Author), J, Anne Rachel (Author)
Format: Article
Language:English
Published: Department of Surgery, UKM Medical Centre, 2014-06-01.
Subjects:
Online Access:Get fulltext
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100 1 0 |a AI, Roger  |e author 
700 1 0 |a J, Anne Rachel  |e author 
245 0 0 |a Congenital Urethrocutaneous Fistula: An Interesting Case. 
260 |b Department of Surgery, UKM Medical Centre,   |c 2014-06-01. 
856 |z Get fulltext  |u http://journalarticle.ukm.my/8354/1/13-MS1184_%2845-47%29.pdf 
520 |a A congenital urethrocutaneous fistula is a rare anomaly which was first described in 1962 by Gupta. Clinically, children present when their guardian is alarmed by either frequent urinary dribbling or unusual stream when they pass urine. This congenital anomaly can present in isolation or be accompanied by a chordee, hypospadia and anorectal malformations in a newborn. The surgical management will either be a primary repair of the fistula or converting it to a hypospadia before proceeding with a single or staged hypospadia repair. Surgical technique will depend on the local tissue factors and associated anomalies. 
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650 0 4 |a R Medicine (General)