Intraductal papillary-mucinous tumor of the pancreas head with complete absence of the ventral pancreatic duct of Wirsung.

Yoichi Sakurai, Toshiki Matsubara, Hiroki Imazu, Shigeru Hasegawa, Shuichi Miyakawa, Masahiro Ochiai, Takahiko Funabiki, Yoshikazu Mizoguchi, Makoto Kuroda
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引用次数: 21

Abstract

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.

胰头导管内乳头状粘液瘤,完全没有Wirsung腹侧胰管。
本文报告一例胰腺导管内乳头状黏液性肿瘤,其腹侧胰管完全缺失。一名74岁日本男性因血清淀粉酶浓度升高而入院。腹部计算机断层扫描(CT)显示主胰管弥漫性扩张和胰头弥漫性无边界密度不均的区域。内镜逆行胰胆管造影显示主胰管与副乳头相连,呈弥漫性扩张,整个胰管长度未见管壁不规则。仅通过沃特氏乳头插管检查胆总管,未见胰管及其通讯分支。一些分支,指向胰头的背侧部分,发现起源于副胰管。经副乳头及胆总管行导管内超声检查,发现胰头一小肿瘤,回声不均一。根据这些发现,诊断为胰头发生的导管内乳头状粘液瘤(IPMT),并行保留幽门的胰十二指肠切除术。切除标本显示胰腺头部有IPMT。切除标本的x线检查显示,肿瘤位于与副乳头相连的胰管,并显示与Vater乳头相连的胰管完全缺失。手术切除使我们能够完整地分析胰腺分裂的导管系统。虽然目前尚不清楚IPMT的发病机制与胰管系统胚胎学异常之间是否存在关系,但本病例可能为IPMT的发病机制提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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