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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”...

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Autores principales: Mittal, Tarun, Pulle, Mohan V., Dey, Ashish, Malik, Vinod K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
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.
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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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