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Well-Differentiated Endocrine Carcinoma Originating From the Bile Duct in Association With a Congenital Choledochal Cyst

机译:胆管癌与先天性胆总管囊肿相关的高分化内分泌癌

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摘要

We encountered a rare case of a well-differentiated endocrine carcinoma originating from the bile duct in association with a congenital choledochal cyst (CCC). The patient is a 28-year-old woman referred to our clinic for pruritus. Laboratory data showed mild elevation of serum hepatobiliary enzymes. Computed tomography and magnetic resonance imaging demonstrated pancreatobiliary maljunction and a Todani type IV-A CCC from the inferior bile duct to the bilateral intrahepatic bile ducts. A solid tumor was detected in the middle portion of the common bile duct. Pancreatoduodenectomy and total extrahepatic bile duct resection was performed. Based on pathologic and immunohistochemical examinations, a diagnosis of well-differentiated endocrine carcinoma was made according to the World Health Organization criteria. To our knowledge, this is the third report of a neuroendocrine tumor originating from the bile duct in association with a CCC.
机译:我们遇到了罕见的病例,该病例是由胆管引起的高分化内分泌癌与先天性胆总管囊肿(CCC)相关。该患者是一名28岁的女性,因皮肤瘙痒而转诊至我们的诊所。实验室数据显示血清肝胆酶水平轻度升高。计算机体层摄影术和磁共振成像显示从下胆管到双侧肝内胆管的胰胆管连接不良和Todani IV-A型CCC。在胆总管中部检测到实体瘤。进行胰十二指肠切除术和全肝外胆管切除术。根据病理学和免疫组织化学检查,根据世界卫生组织的标准诊断为高分化内分泌癌。据我们所知,这是来自胆管与CCC相关的神经内分泌肿瘤的第三次报告。

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