| Literature DB >> 30389731 |
Kashish Khanna1, Devendra Kumar Yadav1, Ruchira Nandan1, Prabudh Goel1, Potala Srinivas Rao2.
Abstract
Congenital colonic stenosis is a rare condition with less than 20 cases reported in the literature since 1966. We report an interesting case of a 7-month-old baby girl who presented with features suggestive of acute intestinal obstruction. On exploration, it was a case of ascending colon stenosis with absence of caecum and appendix. A double barrel ileocolostomy was performed. The histopathology confirmed the diagnosis of colonic stenosis and ruled out the presence of Hirschsprung's disease in the distal colon. The child underwent second stage surgery (stoma closure) after 9 months. In complex cases of congenital colonic stenosis, an early decompressive surgery followed by a delayed second stage closure is recommended in patients with poor general condition. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: congenital disorders; gastrointestinal surgery; paediatric surgery
Mesh:
Year: 2018 PMID: 30389731 DOI: 10.1136/bcr-2018-225072
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X