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首页> 外文期刊>Journal of hepato-biliary-pancreatic surgery >Intraductal papillary-mucinous tumor of the pancreas head with complete absence of the ventral pancreatic duct of Wirsung.
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Intraductal papillary-mucinous tumor of the pancreas head with complete absence of the ventral pancreatic duct of Wirsung.

机译:胰头乳头状粘液性肿瘤,Wirsung腹侧胰管完全不存在。

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A case of intraductal papillary mucinous tumor of the pancreas with complete absence of the ventral pancreatic duct of Wirsung is presented. A 74-year-old Japanese man was admitted to our hospital because of elevated serum amylase concentration. Abdominal computed tomography (CT) scanning revealed diffuse dilatation of the main pancreatic duct and a diffuse and uncircumscribed area with heterogeneous density in the pancreas head. Endoscopic retrograde cholangiopancreatography revealed that the main pancreatic duct was connected with an accessory papilla and was diffusely dilated, without any irregularity of the duct wall being observed in the entire length of the duct. The common bile duct was detected only by cannulation through Vater's papilla, and no pancreatic duct or its communicating branch was found. Some branches, directed to the dorsal portion of the pancreas head, were found arising from the accessory pancreatic duct. Intraductal ultrasound examination performed through the accessory papilla and the common bile duct revealed a small tumor with a heterogeneous echo level in the pancreas head. From these findings, intraductal papillary-mucinous tumor (IPMT) occurring in the pancreas head was diagnosed, and pylorus-preserving pancreaticoduodenectomy was performed. The resected specimen revealed IPMT in the pancreas head. A roentgenographic study of the resected specimen revealed a defect caused by the tumor located in the pancreatic duct connected with the accessory papilla and showed that there was complete absence of the pancreatic duct connected with Vater's papilla. Surgical resection enabled us to completely analyze the duct system of pancreas divisum. Although it is not known whether there is a relationship between the pathogenesis of IPMT and embryological anomaly of the pancreatic duct system, this case may provide an insight into the pathogenesis of IPMT.
机译:介绍了一例胰腺导管内乳头状粘液性肿瘤,而Wirsung的腹侧胰管完全不存在。一名74岁的日本男子因血清淀粉酶浓度升高而入院。腹部计算机断层扫描(CT)扫描显示胰腺主导管弥漫性扩张,以及胰头弥漫性和非外接区域,密度不均。内镜逆行胰胆管造影显示,主胰管与副乳头相连并弥散性扩张,在整个管长中均未观察到管壁不规则。仅通过插管通过Vater的乳头来检测胆总管,未发现胰管或其连通分支。发现一些直达胰头背侧的分支是由胰管旁产生的。通过副乳头和胆总管进行的导管内超声检查发现了一个小肿瘤,胰头回声水平不均匀。根据这些发现,诊断出发生在胰头的导管内乳头状粘液性肿瘤(IPMT),并进行了保留幽门的胰十二指肠切除术。切除的标本显示胰头IPMT。对切​​除的标本进行的X射线照相研究表明,由位于与副乳头相连的胰管中的肿瘤引起的缺损,并表明完全没有与Vater乳头相连的胰管。手术切除使我们能够完全分析胰脏胰管系统。尽管尚不知道IPMT的发病机制与胰管系统的胚胎异常之间是否存在关系,但这种情况可能为IPMT的发病机制提供了见识。

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