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Atrésie intestinale iléale: diagnostic anténatale et prise en charge

Ileal atresia is a rare congenital malformation which affects a small percentage of the population, with an incidence of 1 in 5000 cases. It may be suspected and diagnosed by ultrasound at the end of the second and third trimester. Obstetrical and surgical consultation is the key to success here. El...

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Autores principales: Dhibou, Hanane, Bassir, Ahlam, Sami, Nadia, Boukhanni, Lahcen, Fakhir, Bouchra, Asmouki, Hamid, Soummani, Abderraouf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075440/
https://www.ncbi.nlm.nih.gov/pubmed/27800095
http://dx.doi.org/10.11604/pamj.2016.24.240.9807
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author Dhibou, Hanane
Bassir, Ahlam
Sami, Nadia
Boukhanni, Lahcen
Fakhir, Bouchra
Asmouki, Hamid
Soummani, Abderraouf
author_facet Dhibou, Hanane
Bassir, Ahlam
Sami, Nadia
Boukhanni, Lahcen
Fakhir, Bouchra
Asmouki, Hamid
Soummani, Abderraouf
author_sort Dhibou, Hanane
collection PubMed
description Ileal atresia is a rare congenital malformation which affects a small percentage of the population, with an incidence of 1 in 5000 cases. It may be suspected and diagnosed by ultrasound at the end of the second and third trimester. Obstetrical and surgical consultation is the key to success here. Eliminating a systemic disease with poor prognosis, fighting to reduce premature births and immediately entrusting the child to the surgeon are the main objectives to achieve. During surgery, the surgeon will determine the type of atresia, its location, single or multiple areas of occlusion and its length; thus surgery depends on etiology. Our study reports an interesting clinical case of ileal atresia diagnosed antenatall.
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spelling pubmed-50754402016-10-31 Atrésie intestinale iléale: diagnostic anténatale et prise en charge Dhibou, Hanane Bassir, Ahlam Sami, Nadia Boukhanni, Lahcen Fakhir, Bouchra Asmouki, Hamid Soummani, Abderraouf Pan Afr Med J Case Report Ileal atresia is a rare congenital malformation which affects a small percentage of the population, with an incidence of 1 in 5000 cases. It may be suspected and diagnosed by ultrasound at the end of the second and third trimester. Obstetrical and surgical consultation is the key to success here. Eliminating a systemic disease with poor prognosis, fighting to reduce premature births and immediately entrusting the child to the surgeon are the main objectives to achieve. During surgery, the surgeon will determine the type of atresia, its location, single or multiple areas of occlusion and its length; thus surgery depends on etiology. Our study reports an interesting clinical case of ileal atresia diagnosed antenatall. The African Field Epidemiology Network 2016-07-15 /pmc/articles/PMC5075440/ /pubmed/27800095 http://dx.doi.org/10.11604/pamj.2016.24.240.9807 Text en © Hanane Dhibou 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
Dhibou, Hanane
Bassir, Ahlam
Sami, Nadia
Boukhanni, Lahcen
Fakhir, Bouchra
Asmouki, Hamid
Soummani, Abderraouf
Atrésie intestinale iléale: diagnostic anténatale et prise en charge
title Atrésie intestinale iléale: diagnostic anténatale et prise en charge
title_full Atrésie intestinale iléale: diagnostic anténatale et prise en charge
title_fullStr Atrésie intestinale iléale: diagnostic anténatale et prise en charge
title_full_unstemmed Atrésie intestinale iléale: diagnostic anténatale et prise en charge
title_short Atrésie intestinale iléale: diagnostic anténatale et prise en charge
title_sort atrésie intestinale iléale: diagnostic anténatale et prise en charge
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075440/
https://www.ncbi.nlm.nih.gov/pubmed/27800095
http://dx.doi.org/10.11604/pamj.2016.24.240.9807
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