A Giant Choledochal Cyst Mimicking Pancreatic Pseudocyst: A Case Report. 2022

Fathia Harrabi, and Houssem Ammar, and Mahdi Ben Latifa, and Mohamed Amine Said, and Raoudha Chrigui, and Habiba Ben Hamada, and Rahul Gupta, and Mohamed Ben Mabrouk, and Ali Ben Ali
Gastrointestinal Surgery, Sahloul Hospital, University of Sousse, Sousse, TUN.

A choledochal cyst (CC) is a rare congenital anomaly manifested as cystic dilatation of the biliary tree. A giant choledochal cyst is defined as a cyst with a maximum diameter of ≥ 10 cm. It is an unusual entity and rarely revealed in adulthood. We describe the case of a giant, infected CC presenting as acute pancreatitis with results of abdominal ultrasound and computed tomography consistent with a pancreatic pseudocyst. The diagnosis of CC was made on magnetic resonance cholangiopancreatography (MRCP) findings. We proceeded with cholecystectomy and the complete resection of the diverticulum after its dissection. The defect in the common bile duct was closed transversally over a T-tube. At the last follow-up two years after his admission, the patient is symptom-free with normal liver enzymes To the best of our knowledge, this is the first case reported of giant CC complicated with both infection and pancreatitis.

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