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Spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature

BACKGROUND: Spontaneous biliary system perforation is a rare presentation in clinical practice especially in adults. It is rarely suspected and diagnosed preoperatively due to small number of cases, vague sign and symptoms, and ambiguous presentation. CASE PRESENTATION: We describe an interesting ca...

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Autores principales: Masroor, Matiullah, Sarwari, Mohammad Arif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106123/
https://www.ncbi.nlm.nih.gov/pubmed/33964909
http://dx.doi.org/10.1186/s12893-021-01230-2
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author Masroor, Matiullah
Sarwari, Mohammad Arif
author_facet Masroor, Matiullah
Sarwari, Mohammad Arif
author_sort Masroor, Matiullah
collection PubMed
description BACKGROUND: Spontaneous biliary system perforation is a rare presentation in clinical practice especially in adults. It is rarely suspected and diagnosed preoperatively due to small number of cases, vague sign and symptoms, and ambiguous presentation. CASE PRESENTATION: We describe an interesting case of spontaneous perforation of the common bile duct in a 16 year-old female who presented a week after her first birth to the emergency department with complaints of diffuse abdominal pain, abdominal distention, fever, vomiting, and constipation. She was having generalized peritonitis but the etiology was unclear despite a thorough workup. She underwent exploratory laparotomy, and a perforation in the supra duodenal region of the common bile duct was found intraoperatively. The common bile duct was repaired over T-tube, and cholecystectomy was performed; the patient was recovered uneventfully. CONCLUSION: Spontaneous biliary perforation is a rare cause of acute abdomen in adults and extremely rare in pregnancy. Its delayed diagnoses and management can lead to a high morbidity and mortality. All physicians, especially surgeons, should be aware of this possibility and consider it a cause of peritonitis on differential diagnosis particularly when there is no apparent etiology available for presentation.
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spelling pubmed-81061232021-05-10 Spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature Masroor, Matiullah Sarwari, Mohammad Arif BMC Surg Case Report BACKGROUND: Spontaneous biliary system perforation is a rare presentation in clinical practice especially in adults. It is rarely suspected and diagnosed preoperatively due to small number of cases, vague sign and symptoms, and ambiguous presentation. CASE PRESENTATION: We describe an interesting case of spontaneous perforation of the common bile duct in a 16 year-old female who presented a week after her first birth to the emergency department with complaints of diffuse abdominal pain, abdominal distention, fever, vomiting, and constipation. She was having generalized peritonitis but the etiology was unclear despite a thorough workup. She underwent exploratory laparotomy, and a perforation in the supra duodenal region of the common bile duct was found intraoperatively. The common bile duct was repaired over T-tube, and cholecystectomy was performed; the patient was recovered uneventfully. CONCLUSION: Spontaneous biliary perforation is a rare cause of acute abdomen in adults and extremely rare in pregnancy. Its delayed diagnoses and management can lead to a high morbidity and mortality. All physicians, especially surgeons, should be aware of this possibility and consider it a cause of peritonitis on differential diagnosis particularly when there is no apparent etiology available for presentation. BioMed Central 2021-05-08 /pmc/articles/PMC8106123/ /pubmed/33964909 http://dx.doi.org/10.1186/s12893-021-01230-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Masroor, Matiullah
Sarwari, Mohammad Arif
Spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature
title Spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature
title_full Spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature
title_fullStr Spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature
title_full_unstemmed Spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature
title_short Spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature
title_sort spontaneous common bile duct perforation in full term pregnancy: a rare case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106123/
https://www.ncbi.nlm.nih.gov/pubmed/33964909
http://dx.doi.org/10.1186/s12893-021-01230-2
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