Intraductal papillary mucinous neoplasm of the pancreas in a patient with attenuated familial adenomatous polyposis

被引:38
作者
Chetty, R
Salahshor, S
Bapat, B
Berk, T
Croitoru, M
Gallinger, S
机构
[1] Princess Margaret Hosp, Univ Hlth Network, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Pathol, Dept Lab Med & Pathobiol, Toronto, ON M5G 2M9, Canada
[3] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Familial GI Canc Registry, Toronto, ON M5G 1X5, Canada
[4] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Ctr Canc Genet, Toronto, ON M5G 1X5, Canada
[5] Ontario Canc Inst, Dept Med Biophys, Toronto, ON, Canada
[6] Univ Toronto, Dept Surg, Toronto, ON, Canada
关键词
D O I
10.1136/jcp.2004.020925
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A 67 year old man with a clinical diagnosis of attenuated familial adenomatous polyposis ( AFAP) and a past history of synchronous colon cancers in the transverse colon was also found to have an intraductal papillary mucinous neoplasm (IPMN) of the pancreas. In addition, several foci of heterotopic gastric oxyntic mucosa were noted in the duodenum, interspersed with flat and polypoid adenomas. The duodenal adenomas showed low grade dysplasia, loss of adenomatous polyposis coli (APC) protein expression, but retention of beta catenin staining, localised to the nucleus and cytoplasm. The IPMN in the pancreas showed an identical immunohistochemical profile to the duodenal adenomas. The heterotopic gastric foci in the duodenum were negative for the APC protein, and b catenin staining was membranous in location. Although the patient did not show germline truncating APC mutations or mutations in the MYH gene, the past history, clinical features, and immunohistochemical profile of the various lesions suggest strongly that the IPMN is part of the spectrum of lesions encountered in AFAP. Whether the heterotopic oxyntic gastric mucosa in the duodenum is also related is unclear, but it may represent a forme fruste of fundic gland polyps.
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页码:97 / 101
页数:5
相关论文
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  • [31] Zygulska Aneta, 1997, Polish Journal of Pathology, V48, P201