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Hernie de Bochdaleck étranglée: cause rare d’occlusion intestinale aiguë

We report the case of a 28 year old young man with congenital diaphragmatic hernia, detected at a later stage due to occlusive syndrome manifesting on the scanner as small intestine and colonic distension upstream of a strangulated Bochdalek’s diaphragmatic hernia. The patient underwent laparotomy w...

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Autores principales: Iken, Mustapha, Mai, Adil, Choukrad, Fatimzahra, Haloua, Meryem, Lamrani, My Youssef Alaoui, Boubbou, Meryem, Maâroufi, Mustapha, Alami, Badreedddine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945681/
https://www.ncbi.nlm.nih.gov/pubmed/31934233
http://dx.doi.org/10.11604/pamj.2019.34.90.18427
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author Iken, Mustapha
Mai, Adil
Choukrad, Fatimzahra
Haloua, Meryem
Lamrani, My Youssef Alaoui
Boubbou, Meryem
Maâroufi, Mustapha
Alami, Badreedddine
author_facet Iken, Mustapha
Mai, Adil
Choukrad, Fatimzahra
Haloua, Meryem
Lamrani, My Youssef Alaoui
Boubbou, Meryem
Maâroufi, Mustapha
Alami, Badreedddine
author_sort Iken, Mustapha
collection PubMed
description We report the case of a 28 year old young man with congenital diaphragmatic hernia, detected at a later stage due to occlusive syndrome manifesting on the scanner as small intestine and colonic distension upstream of a strangulated Bochdalek’s diaphragmatic hernia. The patient underwent laparotomy with reduction of the hernia and closure of the diaphragmatic rupture. This study aims to update the current understanding of a rare cause of intestinal obstruction, strangulated Bochdalek’s diaphragmatic hernia, whose diagnosis is essentially based on radiological examinations based on the scanner data, which allows early management.
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spelling pubmed-69456812020-01-13 Hernie de Bochdaleck étranglée: cause rare d’occlusion intestinale aiguë Iken, Mustapha Mai, Adil Choukrad, Fatimzahra Haloua, Meryem Lamrani, My Youssef Alaoui Boubbou, Meryem Maâroufi, Mustapha Alami, Badreedddine Pan Afr Med J Case Report We report the case of a 28 year old young man with congenital diaphragmatic hernia, detected at a later stage due to occlusive syndrome manifesting on the scanner as small intestine and colonic distension upstream of a strangulated Bochdalek’s diaphragmatic hernia. The patient underwent laparotomy with reduction of the hernia and closure of the diaphragmatic rupture. This study aims to update the current understanding of a rare cause of intestinal obstruction, strangulated Bochdalek’s diaphragmatic hernia, whose diagnosis is essentially based on radiological examinations based on the scanner data, which allows early management. The African Field Epidemiology Network 2019-10-16 /pmc/articles/PMC6945681/ /pubmed/31934233 http://dx.doi.org/10.11604/pamj.2019.34.90.18427 Text en © Mustapha Iken et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Iken, Mustapha
Mai, Adil
Choukrad, Fatimzahra
Haloua, Meryem
Lamrani, My Youssef Alaoui
Boubbou, Meryem
Maâroufi, Mustapha
Alami, Badreedddine
Hernie de Bochdaleck étranglée: cause rare d’occlusion intestinale aiguë
title Hernie de Bochdaleck étranglée: cause rare d’occlusion intestinale aiguë
title_full Hernie de Bochdaleck étranglée: cause rare d’occlusion intestinale aiguë
title_fullStr Hernie de Bochdaleck étranglée: cause rare d’occlusion intestinale aiguë
title_full_unstemmed Hernie de Bochdaleck étranglée: cause rare d’occlusion intestinale aiguë
title_short Hernie de Bochdaleck étranglée: cause rare d’occlusion intestinale aiguë
title_sort hernie de bochdaleck étranglée: cause rare d’occlusion intestinale aiguë
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945681/
https://www.ncbi.nlm.nih.gov/pubmed/31934233
http://dx.doi.org/10.11604/pamj.2019.34.90.18427
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