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Congenital urethrocutaneous fistula: Case report with review of literature
We are presenting two cases of congenital urethrocutaneous fistula on ventral penile shaft. Congenital urethral fistula is an extremely rare, but easily manageable anomaly that may be confused with hypospadias. Awareness of the entity will avoid complications. This condition may be associated with o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580363/ https://www.ncbi.nlm.nih.gov/pubmed/23450670 http://dx.doi.org/10.4103/0970-0358.105979 |
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author | Bhatnagar, Ankur Upadhyaya, Vijai D. Kumar, Basant |
author_facet | Bhatnagar, Ankur Upadhyaya, Vijai D. Kumar, Basant |
author_sort | Bhatnagar, Ankur |
collection | PubMed |
description | We are presenting two cases of congenital urethrocutaneous fistula on ventral penile shaft. Congenital urethral fistula is an extremely rare, but easily manageable anomaly that may be confused with hypospadias. Awareness of the entity will avoid complications. This condition may be associated with other anomalies like congenital hernias and anorectal malformations. Treatment of this entity is individualized according to site of fistula, associated anomalies and condition of the distal urethra. All the principles of hypospadias surgery should be strictly followed. |
format | Online Article Text |
id | pubmed-3580363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35803632013-02-28 Congenital urethrocutaneous fistula: Case report with review of literature Bhatnagar, Ankur Upadhyaya, Vijai D. Kumar, Basant Indian J Plast Surg Case Report We are presenting two cases of congenital urethrocutaneous fistula on ventral penile shaft. Congenital urethral fistula is an extremely rare, but easily manageable anomaly that may be confused with hypospadias. Awareness of the entity will avoid complications. This condition may be associated with other anomalies like congenital hernias and anorectal malformations. Treatment of this entity is individualized according to site of fistula, associated anomalies and condition of the distal urethra. All the principles of hypospadias surgery should be strictly followed. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3580363/ /pubmed/23450670 http://dx.doi.org/10.4103/0970-0358.105979 Text en Copyright: © Indian Journal of Plastic Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bhatnagar, Ankur Upadhyaya, Vijai D. Kumar, Basant Congenital urethrocutaneous fistula: Case report with review of literature |
title | Congenital urethrocutaneous fistula: Case report with review of literature |
title_full | Congenital urethrocutaneous fistula: Case report with review of literature |
title_fullStr | Congenital urethrocutaneous fistula: Case report with review of literature |
title_full_unstemmed | Congenital urethrocutaneous fistula: Case report with review of literature |
title_short | Congenital urethrocutaneous fistula: Case report with review of literature |
title_sort | congenital urethrocutaneous fistula: case report with review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580363/ https://www.ncbi.nlm.nih.gov/pubmed/23450670 http://dx.doi.org/10.4103/0970-0358.105979 |
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