Urgent cholecystectomy in patient with left-sided gallbladder. Case report and review of the literature


COD: 25_05_2020_3234_ep Categorie: , ,

Annamaria Di Bella, Alessandro Bruscino, Giovanni Alemanno, Carlo Bergamini, Alessio Giordano, Veronica Iacopini, Damiano Bisogni, Paolo Prosperi
Ann Ital Chir, Digital Edition 2020, 9
Epub, May 25

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INTRODUCTION: Sinistroposition of the gallbladder, or true left-sided gallbladder (LSG) without situs viscerum inversus, is a rare congenital anatomical variant where the gallbladder is located to the left of round/falciform ligament. It can be associated with anomalies of the biliary tree, portal system and hepatic vascularization. The surgical management of a LSG could be challenging even for an experienced operator, being usually an incidental intraoperative finding.
CASE REPORT: A 72 years old woman was admitted to our emergency department because of acute cholecystitis. There were no pre-operative indications of sinistroposition of the gallbladder and its aberrant position was discovered during the explorative laparoscopy; because of the unusual anatomy and chronic flogosis, the laparoscopic approach was converted to open surgery. The patient underwent a successful intervention and was discharged after 4 days without complications. Her family history revealed a daughter with biliary atresia.
DISCUSSION: LSG could remain undetected at preoperative imaging, but today, with advances in diagnostic imaging, the report of this condition has increased. Several hypothesis suggest the presence of an underlying embriologic mechanism for LSG and its associated anomalies, but its etiology is still unknown. The association with the daughter’s biliary atresia makes reasonable a possible genetic correlation with this condition.
CONCLUSIONS: In case of LSG, laparoscopic cholecystectomy could be feasible and safe, but with an increased risk of injury to the major biliary structures, mostly in case of severe and chronic inflammation of the gallbladder. Surgeons have to know this variant because of its associated hepatic anomalies.