Congenital multiple colonic atresias with intestinal malrotation: a case report

Abstract Background Congenital intestinal atresia develops in 1 in 1500 to 20,000 births. Colonic atresia, which accounts for 1.8–15% of intestinal atresia cases, is accompanied by other gastrointestinal atresias such as small intestinal atresia, gastroschisis, imperforate anus, and intestinal malfo...

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Main Authors: Daisuke Ishii, Hisayuki Miyagi, Masatoshi Hirasawa, Kazutoshi Miyamoto
Format: Article
Language:English
Published: SpringerOpen 2020-03-01
Series:Surgical Case Reports
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40792-020-00822-z
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spelling doaj-68d2b89414b64dd4bbf4a139c8ef5ebb2020-11-25T02:52:09ZengSpringerOpenSurgical Case Reports2198-77932020-03-01611510.1186/s40792-020-00822-zCongenital multiple colonic atresias with intestinal malrotation: a case reportDaisuke Ishii0Hisayuki Miyagi1Masatoshi Hirasawa2Kazutoshi Miyamoto3Department of Pediatric Surgery, Asahikawa Medical UniversityDepartment of Pediatric Surgery, Asahikawa Medical UniversityDepartment of Pediatric Surgery, Asahikawa Medical UniversityDepartment of Pediatric Surgery, Asahikawa Medical UniversityAbstract Background Congenital intestinal atresia develops in 1 in 1500 to 20,000 births. Colonic atresia, which accounts for 1.8–15% of intestinal atresia cases, is accompanied by other gastrointestinal atresias such as small intestinal atresia, gastroschisis, imperforate anus, and intestinal malformation in 47–80%. Although a report shows that patients with multiple colonic atresias are 8.9% of those with colonic atresia. Case presentation A male infant did not have the first bowel movement within 36 h of birth and had abdominal distention/vomiting. Radiography showed significant dilation of the intestinal tract. A contrast enema examination at 3 days of age showed a microcolon and disruption in the descending colon. We performed an emergency decompressive loop enterostomy in the distended segment. At the age of 7 months, imaging from the stoma showed disruption of the contrast medium in the intestinal tract at the right lower abdomen, and the continuity of the intestinal tract was not clarified. Intestinal malrotation was found during the second surgery, and the enterostomy was located in the ileum proximal to Bauhin’s valve. Continuity of the intestinal serosal surface was maintained. However, multiple membranous obstructions (three atresias and one stenosis) were observed in the distal segment of the bowel, which was penetrated by intraluminal advancement of a urethral catheter. Therefore, he was diagnosed with multiple colonic atresias. The intestinal tract was longitudinally incised, and membranectomy and mucosal/lateral suture were performed. Conclusions It is important for neonates with intestinal atresia to evaluate and prepare for distal patency of the colon before radical anastomosis. In addition, anomalies associated with colon atresia should also be assessed.http://link.springer.com/article/10.1186/s40792-020-00822-zColonic atresiaMultipleIntestinal malrotationMicrocolon
collection DOAJ
language English
format Article
sources DOAJ
author Daisuke Ishii
Hisayuki Miyagi
Masatoshi Hirasawa
Kazutoshi Miyamoto
spellingShingle Daisuke Ishii
Hisayuki Miyagi
Masatoshi Hirasawa
Kazutoshi Miyamoto
Congenital multiple colonic atresias with intestinal malrotation: a case report
Surgical Case Reports
Colonic atresia
Multiple
Intestinal malrotation
Microcolon
author_facet Daisuke Ishii
Hisayuki Miyagi
Masatoshi Hirasawa
Kazutoshi Miyamoto
author_sort Daisuke Ishii
title Congenital multiple colonic atresias with intestinal malrotation: a case report
title_short Congenital multiple colonic atresias with intestinal malrotation: a case report
title_full Congenital multiple colonic atresias with intestinal malrotation: a case report
title_fullStr Congenital multiple colonic atresias with intestinal malrotation: a case report
title_full_unstemmed Congenital multiple colonic atresias with intestinal malrotation: a case report
title_sort congenital multiple colonic atresias with intestinal malrotation: a case report
publisher SpringerOpen
series Surgical Case Reports
issn 2198-7793
publishDate 2020-03-01
description Abstract Background Congenital intestinal atresia develops in 1 in 1500 to 20,000 births. Colonic atresia, which accounts for 1.8–15% of intestinal atresia cases, is accompanied by other gastrointestinal atresias such as small intestinal atresia, gastroschisis, imperforate anus, and intestinal malformation in 47–80%. Although a report shows that patients with multiple colonic atresias are 8.9% of those with colonic atresia. Case presentation A male infant did not have the first bowel movement within 36 h of birth and had abdominal distention/vomiting. Radiography showed significant dilation of the intestinal tract. A contrast enema examination at 3 days of age showed a microcolon and disruption in the descending colon. We performed an emergency decompressive loop enterostomy in the distended segment. At the age of 7 months, imaging from the stoma showed disruption of the contrast medium in the intestinal tract at the right lower abdomen, and the continuity of the intestinal tract was not clarified. Intestinal malrotation was found during the second surgery, and the enterostomy was located in the ileum proximal to Bauhin’s valve. Continuity of the intestinal serosal surface was maintained. However, multiple membranous obstructions (three atresias and one stenosis) were observed in the distal segment of the bowel, which was penetrated by intraluminal advancement of a urethral catheter. Therefore, he was diagnosed with multiple colonic atresias. The intestinal tract was longitudinally incised, and membranectomy and mucosal/lateral suture were performed. Conclusions It is important for neonates with intestinal atresia to evaluate and prepare for distal patency of the colon before radical anastomosis. In addition, anomalies associated with colon atresia should also be assessed.
topic Colonic atresia
Multiple
Intestinal malrotation
Microcolon
url http://link.springer.com/article/10.1186/s40792-020-00822-z
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