A Resected Case of Synchronous Intraductal Papillary Mucinous Adenocarcinoma and Bile Duct Carcinoma

A 76-year-old man referred for jaundice and upper right quadrant pain was found in computed tomography (CT) and MRCP to have a 3cm multilocular cystic lesion in the pancreas head. The bile duct close to the pancreatic lesion was stenotic and the wall had thickened. Endoscopy showed an enlarged orifi...

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Published inNippon Shokaki Geka Gakkai zasshi Vol. 39; no. 5; pp. 596 - 601
Main Authors Hiyoshi, Masahide, Uchiyama, Shuichiro, Kondo, Kazuhiro, Moriguchi, Kiyoka, Asada, Yushiro, Ohuchida, Jiro, Chijiiwa, Kazuo, Nagano, Motoaki, Kai, Masahiro
Format Journal Article
LanguageJapanese
Published The Japanese Society of Gastroenterological Surgery 2006
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ISSN0386-9768
1348-9372
DOI10.5833/jjgs.39.596

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Summary:A 76-year-old man referred for jaundice and upper right quadrant pain was found in computed tomography (CT) and MRCP to have a 3cm multilocular cystic lesion in the pancreas head. The bile duct close to the pancreatic lesion was stenotic and the wall had thickened. Endoscopy showed an enlarged orifice of the papilla Vater with mucous secretion. The multilocular cystic lesion communicating with the main pancreatic duct (MPD) was observed in the pancreas head by ERCP and the MPD was dilated and filled with mucin. The pathological diagnosis of the biopsy specimen from the stenotic bile duct lesion was adenocarcinoma. EUS showed thickening of the septums, but no mural nodule. Pylorus-preserving pancreaticoduodenectomy with D2 lymph node dissection was conducted. The definitive pathological diagnosis was carcinoma of the bile duct invading to the subserosal layer and noninvasive intraductal papillary mucinous carcinoma of the pancreas. These were separately presented and diagnosed as synchronous double cancer. Clinical stage was IVa according to paraaortic lymph node metastasis (16b1). Since, to our knowledge, only 1 case of intraductal papillary mucinous carcinoma associated with bile duct carcinoma has been reported in the literature, we report our case in detail.
ISSN:0386-9768
1348-9372
DOI:10.5833/jjgs.39.596