Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology

An 11-year-old boy underwent ligation of sac for left congenital hydrocele. In the immediate postoperative period, he developed bleeding per rectum and obstructive features. Intramural hematoma of sigmoid colon was detected in diagnostic laparoscopy and confirmed by laparotomy. Sigmoidectomy with co...

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Detalles Bibliográficos
Autores principales: Jagannathan, Muthukumaran, Krishnamurthy, Gautham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913908/
https://www.ncbi.nlm.nih.gov/pubmed/29699360
http://dx.doi.org/10.5005/jp-journals-10018-1114
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author Jagannathan, Muthukumaran
Krishnamurthy, Gautham
author_facet Jagannathan, Muthukumaran
Krishnamurthy, Gautham
author_sort Jagannathan, Muthukumaran
collection PubMed
description An 11-year-old boy underwent ligation of sac for left congenital hydrocele. In the immediate postoperative period, he developed bleeding per rectum and obstructive features. Intramural hematoma of sigmoid colon was detected in diagnostic laparoscopy and confirmed by laparotomy. Sigmoidectomy with colorectal anastomosis was done. Postoperative period was uneventful. How to cite this article: Jagannathan M, Krishnamurthy G. Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology. Euroasian J Hepato-Gastroenterol 2014;4(2):110-112.
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spelling pubmed-59139082018-04-25 Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology Jagannathan, Muthukumaran Krishnamurthy, Gautham Euroasian J Hepatogastroenterol Case Report An 11-year-old boy underwent ligation of sac for left congenital hydrocele. In the immediate postoperative period, he developed bleeding per rectum and obstructive features. Intramural hematoma of sigmoid colon was detected in diagnostic laparoscopy and confirmed by laparotomy. Sigmoidectomy with colorectal anastomosis was done. Postoperative period was uneventful. How to cite this article: Jagannathan M, Krishnamurthy G. Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology. Euroasian J Hepato-Gastroenterol 2014;4(2):110-112. Jaypee Brothers Medical Publishers 2014 2014-07-28 /pmc/articles/PMC5913908/ /pubmed/29699360 http://dx.doi.org/10.5005/jp-journals-10018-1114 Text en Copyright © 2014; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Case Report
Jagannathan, Muthukumaran
Krishnamurthy, Gautham
Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology
title Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology
title_full Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology
title_fullStr Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology
title_full_unstemmed Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology
title_short Postoperative Sigmoid Apoplexy: A Rare Entity in Pediatric Gastroenterology
title_sort postoperative sigmoid apoplexy: a rare entity in pediatric gastroenterology
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913908/
https://www.ncbi.nlm.nih.gov/pubmed/29699360
http://dx.doi.org/10.5005/jp-journals-10018-1114
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