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A rare case of periampullary carcinoma with ectopic ending of Vater’s ampulla

机译:壶腹周围癌的罕见病例异位末端为Vater壶腹

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摘要

A 71-year-old woman was referred to our department complaining of painless progressive jaundice for the last 3 mo. Magnetic resonance imaging and magnetic resonance cholangiopancreatography (MRCP) showed the ectopic hepatopancreatic ampulla draining into the fourth part of the duodenum adjacent to the duodenojejunal flexure; the irregular morphology of the duodenojejunal flexure likely due to a soft tissue mass. Laparotomy confirmed the presence of the abnormal ampulla of Vater located at the fourth part of the duodenum and a soft tissue tumor about 6 cm × 5 cm × 5 cm with a peduncle adjoining the ampulla. Resection of the tumor, including some peripheral tissue, and a Roux-Y loop anastomosis choledochojejunostomy were performed. Pathological examination indicated an intestinal villous adenoma accompanied by severe dysplasia and focal canceration. Periampullary carcinoma with ectopic ending of the Vater’s ampulla into the fourth part of the duodenum is rather rare. The embryonic genetic background of this anomaly has not yet been fully explained. It is worth mentioning that MRCP is useful for demonstrating anomalies and anatomic variants of the biliary tract system and pancreatic duct.
机译:一名71岁的妇女因过去3个月无痛性进行性黄疸而被转介到我们部门。磁共振成像和磁共振胰胆管造影(MRCP)显示异位肝胰腺壶腹排入十二指肠空肠十二指肠弯曲处的十二指肠第四部分。空肠十二指肠弯曲的不规则形态可能是由于软组织肿块引起的。剖腹术证实存在位于十二指肠第四部分的Vater异常壶腹和大约6 cm×5 cm×5 cm的软组织肿瘤,并有与花梗邻接的花梗。切除肿瘤,包括一些周围组织,并进行Roux-Y环吻合术,胆总管空肠吻合术。病理检查表明肠道绒毛状腺瘤伴有严重的不典型增生和局灶性癌变。在Vater壶腹异位末端进入十二指肠第四部分的壶腹周围癌非常罕见。这种异常的胚胎遗传背景尚未得到充分解释。值得一提的是,MRCP可用于证明胆道系统和胰管的异常和解剖学变异。

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