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Congenital right hemidiaphragmatic agenesis

Congenital diaphragmatic hernia is a congenital defect of the diaphragm through which intestine and other viscera herniate into the chest. In extreme form of diaphragmatic maldevelopment, there might be a complete agenesis of diaphragm. A 45-day old male infant was presented with fever, cough and re...

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Detalles Bibliográficos
Autores principales: Mirza, Bilal, Bashir, Zahid, Sheikh, Afzal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276035/
https://www.ncbi.nlm.nih.gov/pubmed/22345915
http://dx.doi.org/10.4103/0970-2113.92364
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author Mirza, Bilal
Bashir, Zahid
Sheikh, Afzal
author_facet Mirza, Bilal
Bashir, Zahid
Sheikh, Afzal
author_sort Mirza, Bilal
collection PubMed
description Congenital diaphragmatic hernia is a congenital defect of the diaphragm through which intestine and other viscera herniate into the chest. In extreme form of diaphragmatic maldevelopment, there might be a complete agenesis of diaphragm. A 45-day old male infant was presented with fever, cough and respiratory distress for a week. Chest radiograph showed right-sided congenital diaphragmatic hernia. The patient underwent surgical exploration and found to have an unusual and large defect of right hemidiaphragm. The diaphragm was absent on anterior and lateral aspects of the chest wall and only a small rim of diaphragm was present on posterior aspect. The defect was identified as agenesis of right hemidiaphragm and successfully managed by suturing the posterior rim of diaphragm to the intercostal muscles and ribs. This report describes successful management of hemidiaphragmatic agenesis without incorporating a prosthetic material.
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spelling pubmed-32760352012-02-16 Congenital right hemidiaphragmatic agenesis Mirza, Bilal Bashir, Zahid Sheikh, Afzal Lung India Case Report Congenital diaphragmatic hernia is a congenital defect of the diaphragm through which intestine and other viscera herniate into the chest. In extreme form of diaphragmatic maldevelopment, there might be a complete agenesis of diaphragm. A 45-day old male infant was presented with fever, cough and respiratory distress for a week. Chest radiograph showed right-sided congenital diaphragmatic hernia. The patient underwent surgical exploration and found to have an unusual and large defect of right hemidiaphragm. The diaphragm was absent on anterior and lateral aspects of the chest wall and only a small rim of diaphragm was present on posterior aspect. The defect was identified as agenesis of right hemidiaphragm and successfully managed by suturing the posterior rim of diaphragm to the intercostal muscles and ribs. This report describes successful management of hemidiaphragmatic agenesis without incorporating a prosthetic material. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3276035/ /pubmed/22345915 http://dx.doi.org/10.4103/0970-2113.92364 Text en Copyright: © Lung India 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
Mirza, Bilal
Bashir, Zahid
Sheikh, Afzal
Congenital right hemidiaphragmatic agenesis
title Congenital right hemidiaphragmatic agenesis
title_full Congenital right hemidiaphragmatic agenesis
title_fullStr Congenital right hemidiaphragmatic agenesis
title_full_unstemmed Congenital right hemidiaphragmatic agenesis
title_short Congenital right hemidiaphragmatic agenesis
title_sort congenital right hemidiaphragmatic agenesis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276035/
https://www.ncbi.nlm.nih.gov/pubmed/22345915
http://dx.doi.org/10.4103/0970-2113.92364
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