Isolated congenital agenesis of the gallbladder and cystic duct: report of a case.

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Serval ID
serval:BIB_D41152EDED2D
Type
Article: article from journal or magazin.
Collection
Publications
Title
Isolated congenital agenesis of the gallbladder and cystic duct: report of a case.
Journal
Journal of surgical education
Author(s)
Joliat G.R., Shubert C.R., Farley D.R.
ISSN
1878-7452 (Electronic)
ISSN-L
1878-7452
Publication state
Published
Issued date
2013
Peer-reviewed
Oui
Volume
70
Number
1
Pages
117-120
Language
english
Notes
Publication types: Case Reports ; Journal Article
Publication Status: ppublish
Abstract
Congenital agenesis of the gallbladder and cystic duct represents a rare anomaly of the biliary system. It likely results from an embryologic mishap in the development of the hepatobiliary bud and can occur with other associated malformations. We report the case of congenital absence of the gallbladder and cystic duct incidentally found during laparoscopy in a 44-year-old Caucasian female. Based on the clinical presentation and ultrasonography findings, the patient was presumed to have symptomatic cholelithiasis and chronic cholecystitis. A laparoscopic cholecystectomy was planned. After introducing the laparoscope, the gallbladder and cystic duct were absent and the procedure aborted. Gallbladder and cystic duct agenesis was confirmed by magnetic resonance cholangiopancreatography. We describe here the difficulties with diagnosis and pain management, and review the literature of this rare pathology.
Keywords
Adult, Cholangiopancreatography, Magnetic Resonance, Cystic Duct/abnormalities, Diagnosis, Differential, Female, Gallbladder/abnormalities, Humans, Laparoscopy, Obesity, Morbid, Pain Management
Pubmed
Web of science
Create date
11/02/2021 13:32
Last modification date
03/02/2024 20:49
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