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Congenital absence of the common bile duct: A rare anomaly of extrahepatic biliary tract
Congenital absence of the common bile duct (CBD) is an extremely rare developmental anomaly with right and left hepatic ducts draining directly into the gallbladder (GB). Other synonyms for this clinical condition are “cholecystohepatic ducts”, “transverse lie of the GB” or “interposition of the GB”...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916758/ https://www.ncbi.nlm.nih.gov/pubmed/27279403 http://dx.doi.org/10.4103/0972-9941.181292 |
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author | Mittal, Tarun Pulle, Mohan V. Dey, Ashish Malik, Vinod K. |
author_facet | Mittal, Tarun Pulle, Mohan V. Dey, Ashish Malik, Vinod K. |
author_sort | Mittal, Tarun |
collection | PubMed |
description | Congenital absence of the common bile duct (CBD) is an extremely rare developmental anomaly with right and left hepatic ducts draining directly into the gallbladder (GB). Other synonyms for this clinical condition are “cholecystohepatic ducts”, “transverse lie of the GB” or “interposition of the GB”. The potential for iatrogenic injury is high, because of either inadvertent division or ligation of the ducts. Diagnosis is mostly made intraoperatively, and needs some form of biliary reconstruction. Herein, we are reporting a case of congenital absence of the CBD in a 36-year-old lady that was detected intraoperatively. |
format | Online Article Text |
id | pubmed-4916758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49167582016-07-05 Congenital absence of the common bile duct: A rare anomaly of extrahepatic biliary tract Mittal, Tarun Pulle, Mohan V. Dey, Ashish Malik, Vinod K. J Minim Access Surg Unusual Case Congenital absence of the common bile duct (CBD) is an extremely rare developmental anomaly with right and left hepatic ducts draining directly into the gallbladder (GB). Other synonyms for this clinical condition are “cholecystohepatic ducts”, “transverse lie of the GB” or “interposition of the GB”. The potential for iatrogenic injury is high, because of either inadvertent division or ligation of the ducts. Diagnosis is mostly made intraoperatively, and needs some form of biliary reconstruction. Herein, we are reporting a case of congenital absence of the CBD in a 36-year-old lady that was detected intraoperatively. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4916758/ /pubmed/27279403 http://dx.doi.org/10.4103/0972-9941.181292 Text en Copyright: © 2016 Journal of Minimal Access Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Unusual Case Mittal, Tarun Pulle, Mohan V. Dey, Ashish Malik, Vinod K. Congenital absence of the common bile duct: A rare anomaly of extrahepatic biliary tract |
title | Congenital absence of the common bile duct: A rare anomaly of extrahepatic biliary tract |
title_full | Congenital absence of the common bile duct: A rare anomaly of extrahepatic biliary tract |
title_fullStr | Congenital absence of the common bile duct: A rare anomaly of extrahepatic biliary tract |
title_full_unstemmed | Congenital absence of the common bile duct: A rare anomaly of extrahepatic biliary tract |
title_short | Congenital absence of the common bile duct: A rare anomaly of extrahepatic biliary tract |
title_sort | congenital absence of the common bile duct: a rare anomaly of extrahepatic biliary tract |
topic | Unusual Case |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916758/ https://www.ncbi.nlm.nih.gov/pubmed/27279403 http://dx.doi.org/10.4103/0972-9941.181292 |
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