A case of MUC5AC-positive intraductal neoplasm of the pancreas classified as an intraductal tubulopapillary neoplasm?

被引:12
作者
Muraki, Takashi [1 ]
Uehara, Takeshi [2 ]
Sano, Kenji [2 ]
Oota, Hiroyoshi [3 ]
Yoshizawa, Akihiko [2 ]
Asaka, Shiho [2 ]
Tateishi, Ayako [2 ]
Otsuki, Toshiaki [2 ]
Shingu, Kunihiko [2 ]
Matoba, Hisanori [2 ]
Kobayashi, Shota [2 ]
Ichimata, Shojiro [2 ]
Watanabe, Takayuki [1 ]
Itou, Tetsuya [1 ]
Tanaka, Eiji [1 ]
机构
[1] Shinshu Univ, Sch Med, Dept Med, Gastroenterol, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Sch Med, Dept Lab Med, Matsumoto, Nagano 3908621, Japan
[3] Shinshu Univ, Sch Med, Dept Biomed Lab Sci, Matsumoto, Nagano 3908621, Japan
关键词
Intraductal tubulopapillary neoplasm; Intraductal papillary mucinous neoplasm; Pancreatobiliary type; MUC5AC; WHO; PAPILLARY MUCINOUS NEOPLASMS; K-RAS MUTATIONS; CANCER CELLS; MUC5AC; MALIGNANCY; EXPRESSION; FEATURES; TUMORS;
D O I
10.1016/j.prp.2015.10.009
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
This report describes a unique case of intraductal tubulopapillary neoplasm (ITPN) of the pancreas in order to clarify its oncogenesis and more precisely classify pancreatic intraductal neoplasms. A 74-year-old man visited our institution for follow-up of acute pancreatitis. Imaging examinations revealed a hypovascular intraductal mass in the head of the pancreas with progressive dilation of the pancreatic duct, atrophy of the pancreatic parenchyma, and a non-mucinous appearance. A pancreatoduodenectomy was performed to identify this pancreatic intraductal neoplasm. Macroscopically, the tumor was a solid nodular mass with no visibly secreted mucin obstructing the dilated ducts. Histologically, it had a homogeneous appearance with nodules of back-to-back tubular glands and occasional papillary elements, and there were no apparent transitions to areas with less marked cytoarchitectural atypia. Although the intraductal neoplastic growth corresponded to an ITPN, immunohistochemical staining revealed partial positivity for MUC5AC, for which ITPNs are characteristically negative. Somatic mutations in KRAS, GNAS, BRAF, and PIK3CA were not detected. A loss of MUC5AC expression and mutations in KRAS and GNAS are key elements in the diagnosis of ITPN. Thus, it was difficult to distinguish the present case as a pancreatobiliary-type (PB-type) intraductal papillary mucinous neoplasm (IPMN) or a phenotypic variant of ITPN. As it is possible that some cases of PB-type IPMN and ITPN overlap, the precise classification of these rare lesions may require re-evaluation. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:1034 / 1039
页数:6
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