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Management of Complex Gallstone Disease With Bouveret's and Mirizzi Syndrome: A Case Report With Literature Review
Rami Ayoub1,2, Omaymah Al-Shweiki3, Vandana Basappa Giriradder2
1Hepatobiliary Surgery, Al-Balqa Applied University, Al-Balqa, JOR.
Abstract:
Gallstone disease affects up to 20% of adults, but rare complications include Bouveret's syndrome, occurring in approximately 0.05% of patients with gallstones, and Mirizzi syndrome, with Type Va involving concurrent biliary and enteric fistulae. We report the case of a 64-year-old man with concurrent Bouveret's syndrome and Csendes Type Va Mirizzi syndrome associated with a cholecystoduodenal fistula. An initial laparoscopic cholecystectomy was abandoned due to concern for malignancy. During the same admission, the patient developed gastric outlet obstruction, and imaging confirmed Bouveret's syndrome caused by a large ectopic gallstone. This was managed with robotic-assisted gastrotomy and stone extraction as a damage-control procedure, with definitive biliary surgery deferred because of severe inflammation and unclear anatomy. Subsequent imaging demonstrated a residual Hartmann's pouch stone with Type Va Mirizzi syndrome and a persistent cholecystoduodenal fistula. The patient underwent a robotic subtotal cholecystectomy with intraoperative indocyanine green assessment and endoscopic evaluation. His postoperative course was complicated by peritonitis, bilious and enteric leakage, and intra-abdominal collections, requiring laparoscopic washout, radiological drainage, total parenteral nutrition, and endoscopic retrograde cholangiopancreatography with placement of a covered metal stent for a cystic duct stump leak. The patient recovered with multidisciplinary management and remained well at follow-up. This case illustrates the complexity of managing dual fistula-related gallstone disease and highlights the importance of staged decision-making, detailed imaging, and combined surgical and endoscopic approaches.
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