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- W2076175781 abstract "Choledochal cyst is a rare congenital condition and can present at any age with female preponderance. Incidence is high in Asian as compared to Western countries [1]. Clinical presentation is nonspecific, and complications include pancreatitis, cholangitis, biliary cirrhosis, spontaneous rupture, and malignancy [2]. Incidence of malignancy increases with age. Imaging with contrast enhanced computerized tomography (CECT) and magnetic resonance cholangiopancreatography (MRCP) has facilitated the preoperative suspicion of malignancy, and surgical treatment has evolved from cystoenterostomy to primary cyst excision with bilioenteric drainage [2]. We are reporting a preoperatively suspected case of choledochal cyst with malignancy." @default.
- W2076175781 created "2016-06-24" @default.
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- W2076175781 date "2014-04-27" @default.
- W2076175781 modified "2023-09-23" @default.
- W2076175781 title "Adenocarcinoma in Choledochal Cyst—a Case Report" @default.
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- W2076175781 doi "https://doi.org/10.1007/s12262-014-1073-y" @default.
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