An appendix carcinoid tumor in a patient with hereditary nonpolyposis colorectal cancer

被引:11
作者
Miquel, C
Sabourin, JC
Elias, D
Grandjouan, S
Viguier, J
Ducreux, M
Duvillard, P
Praz, F
机构
[1] St Anne Hosp, Dept Pathol, Paris, France
[2] French Natl Ctr Sci Res, Unit Genet Instabil & Canc 2169, Villejuif, France
[3] Inst Gustave Roussy, Dept Med, Villejuif, France
[4] Inst Gustave Roussy, Dept Surg, Villejuif, France
[5] Cochin Hosp, Dept Gastroenterol, Paris, France
关键词
appendix carcinoid tumor; colorectal cancer; hereditary nonpolyposis colorectal cancer; microsatellite instability;
D O I
10.1016/j.humpath.2004.09.017
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Gastrointestinal carcinoid tumors are often associated with other tumors, particularly colon adenocarcinomas; but the association between carcinoid tumors and hereditary nonpolyposis colorectal cancer (HNPCC) syndrome has not yet been explored. We report an unusual case of a 28-year-old woman with HNPCC who underwent surgery for a transverse colon adenocarcinoma in whom an appendix carcinoid tumor was incidentally found. To assess whether the carcinoid tumor displayed the characteristic molecular features of HNPCC tumors, we investigated the expression of mismatch-repair (MMR) proteins and microsatellite instability (MST) status in both tumors. Both tumors demonstrated normal expression of the MMR proteins hMLH1, hMSH2, hMSH6, and hPMS2. Interestingly, the adenocarcinoma exhibited an MSI phenotype but the carcinoid tumor did not, indicating that these 2 tumors arose through different molecular pathways. Hum PATHOL 35:1564-1567. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1564 / 1567
页数:4
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