Complete Urethral Duplication in Children: A Case Report

INTRODUCTION: Urethral duplication (UD) is a rare congenital anomaly with multiple anatomical variants. CASE PRESENTATION: In this article we present a four year-old child with complete UD. The patient was admitted for hypospadias repair, in evaluation we found type IIA1 UD according to Effmann clas...

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Detalles Bibliográficos
Autores principales: Roshanzamir, Fatollah, Mirshemirani, Alireza, Ghoroubi, Javad, Mahdavi, Alireza, Mohajerzadeh, Leily, Sarafi, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906148/
https://www.ncbi.nlm.nih.gov/pubmed/27307964
http://dx.doi.org/10.5812/ijp.3620
Descripción
Sumario:INTRODUCTION: Urethral duplication (UD) is a rare congenital anomaly with multiple anatomical variants. CASE PRESENTATION: In this article we present a four year-old child with complete UD. The patient was admitted for hypospadias repair, in evaluation we found type IIA1 UD according to Effmann classification. Patient underwent hypospadias repair saving complete UD. CONCLUSIONS: After one year follow-up he has normal and continent urination.

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