Gallbladder diaphragm: about a case

• Published in: International Surgery Journal Vol. 8; no. 7; p. 2159
• Main Authors: Marouane, Baiss, El Majdoubi, Hicham, Mohammed, Rabbani, Rahali, Anwar, Massrouri, Rahal, Said, Benamer, Lahlou, Khalid, Mdaghri, Jalil, Settaf, Abdellatif
• Format: Journal Article
• Language: English
• Published: 28.06.2021
• ISSN: 2349-3305; 2349-2902
• DOI: 10.18203/2349-2902.isj20212725

Diaphragm gallbladder is a very rare anomaly of gallbladder embryogenesis. This malformation is very rare in adults and represents 0.1% of gallbladder anomalies. It can remain asymptomatic for a long time and be discovered fortuitously during a radiological examination for another pathology or be revealed by chronic abdominal pain or by a complication such as cholecystitis or biliary peritonitis. We report the observation of a 34 years old woman with chronic hepatic colic. The biological work-up including a blood count, a hepatic cytolysis and cholestas and CRP determination did not reveal any abnormality, whose morphological examinations concluded to an uncomplicated diaphragm gallbladder. A laparoscopic cholecystectomy was performed. The post-operative course was unremarkable. The intraoperative finding by opening the cholecystectomy specimen confirmed the diagnosis of a diaphragm gallbladder. Histological study confirms the diagnosis of diaphragm vesicle cholecystitis. In this document, we described the clinical and radiological characteristics of this rare anomaly.