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

Détails

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Etat: Public
Version: de l'auteur⸱e
Licence: Non spécifiée
ID Serval
serval:BIB_D41152EDED2D
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Isolated congenital agenesis of the gallbladder and cystic duct: report of a case.
Périodique
Journal of surgical education
Auteur⸱e⸱s
Joliat G.R., Shubert C.R., Farley D.R.
ISSN
1878-7452 (Electronic)
ISSN-L
1878-7452
Statut éditorial
Publié
Date de publication
2013
Peer-reviewed
Oui
Volume
70
Numéro
1
Pages
117-120
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article
Publication Status: ppublish
Résumé
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.
Mots-clé
Adult, Cholangiopancreatography, Magnetic Resonance, Cystic Duct/abnormalities, Diagnosis, Differential, Female, Gallbladder/abnormalities, Humans, Laparoscopy, Obesity, Morbid, Pain Management
Pubmed
Web of science
Création de la notice
11/02/2021 13:32
Dernière modification de la notice
03/02/2024 20:49
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