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Les complications du diverticule de Meckel chez l'enfant: à propos de 18 cas
Meckel’s diverticulum (MD) is a remnant of omphalomesenteric channel. It is often asymptomatic but it can be responsible for various clinical complications and variable clinical status especially in children. We conducted a retrospective study on complications of MD among children hospitalized in th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711690/ https://www.ncbi.nlm.nih.gov/pubmed/31489091 http://dx.doi.org/10.11604/pamj.2019.33.113.18756 |
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author | Charki, Mohammed Tazi Oukhouya, Mohammed-Amine Benmassaoud, Zineb Mahmoudi, Abdelhalim Khattala, Khalid Bouabdallah, Youssef |
author_facet | Charki, Mohammed Tazi Oukhouya, Mohammed-Amine Benmassaoud, Zineb Mahmoudi, Abdelhalim Khattala, Khalid Bouabdallah, Youssef |
author_sort | Charki, Mohammed Tazi |
collection | PubMed |
description | Meckel’s diverticulum (MD) is a remnant of omphalomesenteric channel. It is often asymptomatic but it can be responsible for various clinical complications and variable clinical status especially in children. We conducted a retrospective study on complications of MD among children hospitalized in the division of Paediatric Surgery at the University Hospital Hassan II, Fez, Morocco. The study aimed to describe the clinical, radiological and therapeutic features of MD. The study was conducted over a period of 10 years (January 2009 - December 2018) and involved 18 children (15 boys and 3 girls) aged 1 day - 15 years (with an average age of 5 years) who had undergone surgery for complications of MD. Acute intussusception and intestinal occlusion were the most frequent complications. Other complications included: infection of the MD (1 case) and digestive hemorrhage (2 cases). Two rare types of neonatal Meckel’s diverticulum were described (neonatal occlusion and fistula associated with omphalocele). In no case, abdominal X-ray without treatment, ultrasound and CT scan showed MD. Scintigraphy was performed in 2 patients with hematochezia and it helped to make the diagnosis of MD in one case. Three patients underwent laparoscopic surgery with resection of the MD and intestinal anastomosis with laparoscopy. The other patients underwent laparotomy. Ileostomy was performed in one case, followed by secondary recovery. Patient’s outcome was good, except for one case of anastomotic leakage. Anatomopathological examination showed two cases of heterotopia. |
format | Online Article Text |
id | pubmed-6711690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-67116902019-09-05 Les complications du diverticule de Meckel chez l'enfant: à propos de 18 cas Charki, Mohammed Tazi Oukhouya, Mohammed-Amine Benmassaoud, Zineb Mahmoudi, Abdelhalim Khattala, Khalid Bouabdallah, Youssef Pan Afr Med J Case Series Meckel’s diverticulum (MD) is a remnant of omphalomesenteric channel. It is often asymptomatic but it can be responsible for various clinical complications and variable clinical status especially in children. We conducted a retrospective study on complications of MD among children hospitalized in the division of Paediatric Surgery at the University Hospital Hassan II, Fez, Morocco. The study aimed to describe the clinical, radiological and therapeutic features of MD. The study was conducted over a period of 10 years (January 2009 - December 2018) and involved 18 children (15 boys and 3 girls) aged 1 day - 15 years (with an average age of 5 years) who had undergone surgery for complications of MD. Acute intussusception and intestinal occlusion were the most frequent complications. Other complications included: infection of the MD (1 case) and digestive hemorrhage (2 cases). Two rare types of neonatal Meckel’s diverticulum were described (neonatal occlusion and fistula associated with omphalocele). In no case, abdominal X-ray without treatment, ultrasound and CT scan showed MD. Scintigraphy was performed in 2 patients with hematochezia and it helped to make the diagnosis of MD in one case. Three patients underwent laparoscopic surgery with resection of the MD and intestinal anastomosis with laparoscopy. The other patients underwent laparotomy. Ileostomy was performed in one case, followed by secondary recovery. Patient’s outcome was good, except for one case of anastomotic leakage. Anatomopathological examination showed two cases of heterotopia. The African Field Epidemiology Network 2019-06-14 /pmc/articles/PMC6711690/ /pubmed/31489091 http://dx.doi.org/10.11604/pamj.2019.33.113.18756 Text en © Mohammed Tazi Charki 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 Series Charki, Mohammed Tazi Oukhouya, Mohammed-Amine Benmassaoud, Zineb Mahmoudi, Abdelhalim Khattala, Khalid Bouabdallah, Youssef Les complications du diverticule de Meckel chez l'enfant: à propos de 18 cas |
title | Les complications du diverticule de Meckel chez l'enfant: à propos de 18 cas |
title_full | Les complications du diverticule de Meckel chez l'enfant: à propos de 18 cas |
title_fullStr | Les complications du diverticule de Meckel chez l'enfant: à propos de 18 cas |
title_full_unstemmed | Les complications du diverticule de Meckel chez l'enfant: à propos de 18 cas |
title_short | Les complications du diverticule de Meckel chez l'enfant: à propos de 18 cas |
title_sort | les complications du diverticule de meckel chez l'enfant: à propos de 18 cas |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711690/ https://www.ncbi.nlm.nih.gov/pubmed/31489091 http://dx.doi.org/10.11604/pamj.2019.33.113.18756 |
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