Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease

The incidence of ileal atresia ranges from 1/5000 to 1/12000 births. The incidence of Hirschsprung's disease is 1/5000.The combination of Hirschsprung disease and ileal atresia during infancy seems to be a rare event and the exact incidence of the association of the two malformations remains un...

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Main Authors: I. Belbahri, G. Fusi, Thibault Planchamp T, S. Mouttalib, L. Carfagna, A. Le Mandat, O. Abbo
Format: Article
Language:English
Published: Elsevier 2022-09-01
Series:Journal of Pediatric Surgery Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2213576622001956
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author I. Belbahri
G. Fusi
Thibault Planchamp T
S. Mouttalib
L. Carfagna
A. Le Mandat
O. Abbo
author_facet I. Belbahri
G. Fusi
Thibault Planchamp T
S. Mouttalib
L. Carfagna
A. Le Mandat
O. Abbo
author_sort I. Belbahri
collection DOAJ
description The incidence of ileal atresia ranges from 1/5000 to 1/12000 births. The incidence of Hirschsprung's disease is 1/5000.The combination of Hirschsprung disease and ileal atresia during infancy seems to be a rare event and the exact incidence of the association of the two malformations remains unknown.Several embryo-pathological theories have been offered to explain the correlation of these two malformations. Some of them state that atresia would be a consequence of aganglionnosis and some others the contrary.The urgency of an early detection of this associations is related to her increased morbidity during management, especially if part of the phenotype remains unidentified.To date, less than 25 case of ileal atresia associated with Hirschsprung's disease are reported in Literature.We present two cases managed in our department initially for ileal atresia. Diagnosis of total colonic Hirschsprung's disease associated was placed later, after the appearance of an intestinal occlusion at the time of the restoration of digestive continuity. The first case was derived three times, and the second twice before becoming digestive self-sufficient.The dysfunction of the anastomosis after restoration of continuity is a dangerous complication which underlines the interest of the early diagnosis of the association ileal atresia and Hirschsprung's disease. It is necessary to have the rectal biopsy early, especially when the patient continues to exhibit poor bowel function after corrective surgery.
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spelling doaj.art-a7a0bae14ade4ada8a24f8aaad020c832022-12-22T02:48:37ZengElsevierJournal of Pediatric Surgery Case Reports2213-57662022-09-0184102368Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's diseaseI. Belbahri0G. Fusi1Thibault Planchamp T2S. Mouttalib3L. Carfagna4A. Le Mandat5O. Abbo6Department of Pediatric Surgery, Hôpital des Enfants de Toulouse, CHU Toulouse, 330 Avenue de Grande Bretagne, 31300, Toulouse, FranceCorresponding author.; Department of Pediatric Surgery, Hôpital des Enfants de Toulouse, CHU Toulouse, 330 Avenue de Grande Bretagne, 31300, Toulouse, FranceDepartment of Pediatric Surgery, Hôpital des Enfants de Toulouse, CHU Toulouse, 330 Avenue de Grande Bretagne, 31300, Toulouse, FranceDepartment of Pediatric Surgery, Hôpital des Enfants de Toulouse, CHU Toulouse, 330 Avenue de Grande Bretagne, 31300, Toulouse, FranceDepartment of Pediatric Surgery, Hôpital des Enfants de Toulouse, CHU Toulouse, 330 Avenue de Grande Bretagne, 31300, Toulouse, FranceDepartment of Pediatric Surgery, Hôpital des Enfants de Toulouse, CHU Toulouse, 330 Avenue de Grande Bretagne, 31300, Toulouse, FranceDepartment of Pediatric Surgery, Hôpital des Enfants de Toulouse, CHU Toulouse, 330 Avenue de Grande Bretagne, 31300, Toulouse, FranceThe incidence of ileal atresia ranges from 1/5000 to 1/12000 births. The incidence of Hirschsprung's disease is 1/5000.The combination of Hirschsprung disease and ileal atresia during infancy seems to be a rare event and the exact incidence of the association of the two malformations remains unknown.Several embryo-pathological theories have been offered to explain the correlation of these two malformations. Some of them state that atresia would be a consequence of aganglionnosis and some others the contrary.The urgency of an early detection of this associations is related to her increased morbidity during management, especially if part of the phenotype remains unidentified.To date, less than 25 case of ileal atresia associated with Hirschsprung's disease are reported in Literature.We present two cases managed in our department initially for ileal atresia. Diagnosis of total colonic Hirschsprung's disease associated was placed later, after the appearance of an intestinal occlusion at the time of the restoration of digestive continuity. The first case was derived three times, and the second twice before becoming digestive self-sufficient.The dysfunction of the anastomosis after restoration of continuity is a dangerous complication which underlines the interest of the early diagnosis of the association ileal atresia and Hirschsprung's disease. It is necessary to have the rectal biopsy early, especially when the patient continues to exhibit poor bowel function after corrective surgery.http://www.sciencedirect.com/science/article/pii/S2213576622001956
spellingShingle I. Belbahri
G. Fusi
Thibault Planchamp T
S. Mouttalib
L. Carfagna
A. Le Mandat
O. Abbo
Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease
Journal of Pediatric Surgery Case Reports
title Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease
title_full Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease
title_fullStr Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease
title_full_unstemmed Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease
title_short Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease
title_sort diagnostic challenge of concomitant small bowel atresia and hirschsprung s disease
url http://www.sciencedirect.com/science/article/pii/S2213576622001956
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