A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child

Spontaneous common bile duct (CBD) perforation leading to biliary peritonitis is a rare entity in children. It is an unusual cause of acute abdomen and is potentially fatal. Preoperative diagnosis is rare. A 10-year-old girl was referred from a private hospital after laparotomy for acute abdomen. In...

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Autores principales: Sharma, Charu, Desale, Jayesh, Waghmare, Mukta, Shah, Hemanshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578587/
https://www.ncbi.nlm.nih.gov/pubmed/29201751
http://dx.doi.org/10.5005/jp-journals-10018-1191
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author Sharma, Charu
Desale, Jayesh
Waghmare, Mukta
Shah, Hemanshi
author_facet Sharma, Charu
Desale, Jayesh
Waghmare, Mukta
Shah, Hemanshi
author_sort Sharma, Charu
collection PubMed
description Spontaneous common bile duct (CBD) perforation leading to biliary peritonitis is a rare entity in children. It is an unusual cause of acute abdomen and is potentially fatal. Preoperative diagnosis is rare. A 10-year-old girl was referred from a private hospital after laparotomy for acute abdomen. Intraoperatively, bile was found in the peritoneal cavity which was drained, and the patient was referred to Topiwala National Medical College. Endoscopic retrograde cholangiopancreaticography (ERCP) and stenting was done. The stent was removed after 8 weeks, and the girl is doing well during follow-up. HOW TO CITE THIS ARTICLE: Sharma C, Desale J, Waghmare M, Shah H. A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child. Euroasian J Hepato-Gastroenterol 2016;6(2):167-169.
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spelling pubmed-55785872017-11-30 A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child Sharma, Charu Desale, Jayesh Waghmare, Mukta Shah, Hemanshi Euroasian J Hepatogastroenterol Case Report Spontaneous common bile duct (CBD) perforation leading to biliary peritonitis is a rare entity in children. It is an unusual cause of acute abdomen and is potentially fatal. Preoperative diagnosis is rare. A 10-year-old girl was referred from a private hospital after laparotomy for acute abdomen. Intraoperatively, bile was found in the peritoneal cavity which was drained, and the patient was referred to Topiwala National Medical College. Endoscopic retrograde cholangiopancreaticography (ERCP) and stenting was done. The stent was removed after 8 weeks, and the girl is doing well during follow-up. HOW TO CITE THIS ARTICLE: Sharma C, Desale J, Waghmare M, Shah H. A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child. Euroasian J Hepato-Gastroenterol 2016;6(2):167-169. Jaypee Brothers Medical Publishers 2016 2016-12-01 /pmc/articles/PMC5578587/ /pubmed/29201751 http://dx.doi.org/10.5005/jp-journals-10018-1191 Text en Copyright © 2016; 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
Sharma, Charu
Desale, Jayesh
Waghmare, Mukta
Shah, Hemanshi
A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child
title A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child
title_full A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child
title_fullStr A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child
title_full_unstemmed A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child
title_short A Case of Biliary Peritonitis following Spontaneous Common Bile Duct Perforation in a Child
title_sort case of biliary peritonitis following spontaneous common bile duct perforation in a child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578587/
https://www.ncbi.nlm.nih.gov/pubmed/29201751
http://dx.doi.org/10.5005/jp-journals-10018-1191
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