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High anorectal malformation in a five-month-old boy: a case report

INTRODUCTION: Anorectal malformation, one of the most common congenital defects, may present with a wide spectrum of defects. Almost all male patients present within first few days of life. CASE PRESENTATION: A five-month-old baby boy of Indian origin and nationality presented with anal atresia and...

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Autores principales: Pandey, Anand, Gangopadhyay, Ajay N, Kumar, Vijayendra, Sharma, Shiv P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936323/
https://www.ncbi.nlm.nih.gov/pubmed/20807404
http://dx.doi.org/10.1186/1752-1947-4-296
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author Pandey, Anand
Gangopadhyay, Ajay N
Kumar, Vijayendra
Sharma, Shiv P
author_facet Pandey, Anand
Gangopadhyay, Ajay N
Kumar, Vijayendra
Sharma, Shiv P
author_sort Pandey, Anand
collection PubMed
description INTRODUCTION: Anorectal malformation, one of the most common congenital defects, may present with a wide spectrum of defects. Almost all male patients present within first few days of life. CASE PRESENTATION: A five-month-old baby boy of Indian origin and nationality presented with anal atresia and associated rectourethral prostatic fistula. The anatomy of the malformation and our patient's good condition permitted a primary definitive repair of the anomaly. A brief review of the relevant literature is included. CONCLUSION: Delayed presentation of a patient with high anorectal malformation is rare. The appropriate treatment can be rewarding.
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spelling pubmed-29363232010-09-10 High anorectal malformation in a five-month-old boy: a case report Pandey, Anand Gangopadhyay, Ajay N Kumar, Vijayendra Sharma, Shiv P J Med Case Reports Case Report INTRODUCTION: Anorectal malformation, one of the most common congenital defects, may present with a wide spectrum of defects. Almost all male patients present within first few days of life. CASE PRESENTATION: A five-month-old baby boy of Indian origin and nationality presented with anal atresia and associated rectourethral prostatic fistula. The anatomy of the malformation and our patient's good condition permitted a primary definitive repair of the anomaly. A brief review of the relevant literature is included. CONCLUSION: Delayed presentation of a patient with high anorectal malformation is rare. The appropriate treatment can be rewarding. BioMed Central 2010-08-31 /pmc/articles/PMC2936323/ /pubmed/20807404 http://dx.doi.org/10.1186/1752-1947-4-296 Text en Copyright ©2010 Pandey et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Pandey, Anand
Gangopadhyay, Ajay N
Kumar, Vijayendra
Sharma, Shiv P
High anorectal malformation in a five-month-old boy: a case report
title High anorectal malformation in a five-month-old boy: a case report
title_full High anorectal malformation in a five-month-old boy: a case report
title_fullStr High anorectal malformation in a five-month-old boy: a case report
title_full_unstemmed High anorectal malformation in a five-month-old boy: a case report
title_short High anorectal malformation in a five-month-old boy: a case report
title_sort high anorectal malformation in a five-month-old boy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936323/
https://www.ncbi.nlm.nih.gov/pubmed/20807404
http://dx.doi.org/10.1186/1752-1947-4-296
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