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Case report on a rare cholecystocutaneous fistula and its link to biliary fistulas in gallbladder disease.
Spontaneous cholecystocutaneous abscess or fistula is an exceptionally rare consequence of gallbladderdisease, with fewer than 100 cases reported in the literature. The condition was first described by Thelisus in11670, and later, Courvoisier documented 169 occurrences of biliary fistulas in the 19th century . Biliary2fistulas, which can be internal or external, often arise as a complication of acute calculus cholecystitis. Fromsuppurative cholecystitis with spontaneous rupture to surgical external drainage of an abscess, the disease's3natural course has changed due to medical and surgical interventions have significantly altered its course .The primary underlying mechanism involves obstruction of bile outflow due to gallstones, which increasesintra gallbladder pressure, disrupts lymphatic drainage, and compromises gallbladder wall circulation. Thesepathophysiological changes contribute to necrosis and subsequent fistula formation. If perforation occurs,bile leakage may lead to a localized peritoneal abscess or extend externally through the abdominal wall.Early and effective management of biliary tract disease is critical to preventing this uncommon but severecomplication.
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Gillani et al. (2025) studied this question.
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