Rugge M, Sonego F, Militello C, Guido M, Ninfo V
Cattedra di Istochimica e Immunoistochimica Patologica-Servizio di Anatomia Patologica, Università degli Studi di Padova-ULLS 19 del Mediobrenta, Italy.
Am J Surg Pathol. 1992 Aug;16(8):802-7. doi: 10.1097/00000478-199208000-00010.
We report a case of primary carcinoid tumor arising at the confluence of the cystic and common bile ducts. The patient was a 64-year-old woman who developed a sudden onset of biliary colic and jaundice. Computerized tomography and nuclear magnetic resonance showed a mass lesion close to the head of the pancreas. At laparotomy a nodular lesion was found at the confluence of the cystic and common bile ducts. Microscopic observation revealed a type B-C carcinoid (Soga's classification) with positive immunoreactivity to chromogranin and cytokeratin. The presence of neurosecretory intracytoplasmic granules was demonstrated by electron microscopy. Flow cytometry showed diploid DNA content of the neoplastic cells with less than 5% of the nuclei in the S-phase region.
我们报告一例起源于胆囊管与胆总管汇合处的原发性类癌肿瘤。患者为一名64岁女性,突发胆绞痛和黄疸。计算机断层扫描和核磁共振显示胰腺头部附近有一肿块病变。剖腹手术时,在胆囊管与胆总管汇合处发现一个结节性病变。显微镜观察显示为B - C型类癌(索加分类法),对嗜铬粒蛋白和细胞角蛋白免疫反应呈阳性。电子显微镜证实存在神经分泌性胞浆颗粒。流式细胞术显示肿瘤细胞的DNA含量为二倍体,S期区域的细胞核占比不到5%。