Two Japanese kindreds occurring endometrial cancer meeting new clinical criteria for hereditary non-polyposis colorectal cancer (HNPCC), Amsterdam Criteria II

被引:6
作者
Banno, K
Susumu, N
Hirao, T
Yanokura, M
Hirasawa, A
Aoki, D
Udagawa, Y
Sugano, K
Nozawa, S
机构
[1] Keio Univ, Sch Med, Dept Obstet & Gynecol, Shinjuku Ku, Tokyo 1608582, Japan
[2] Fujita Hlth Univ, Sch Med, Dept Obstet & Gynecol, Nagoya, Aichi, Japan
[3] Tochigi Canc Ctr Res Inst, Oncogene Res Unit, Tochigi, Japan
关键词
endometrial cancer; hereditary non-polyposis colorectal cancer (HNPCC); hMLH1; hMSH2; hMSH6;
D O I
10.1111/j.1447-0756.2004.00195.x
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Hereditary non-polyposis colorectal cancer (HNPCC), also called Lynch syndrome, is an autosomal dominantly inherited disorder of cancer susceptibility. Patients with HNPCC exhibit an increased risk for HNPCC-associated extracolonic tumors such as cancer of the endometrium. HNPCC is associated with germline mutations in DNA mismatch repair (MMR) genes: hMLH1, hMSH2 and hMSH6. Here, we describe two Japanese kindreds (0.5%) who met the new clinical criteria for HNPCC, Amsterdam criteria II, from among 375 endometrial cancer patients treated at Keio University Hospital from 1990 to 2002. From these results, it was found that female HNPCC patients comprised approximately 0.5% of all endometrial cancer patients. Decreased expression of two MMR gene protein products (hMLH1 and hMSH6) was confirmed immunohistochemically in these two endometrial tumors in HNPCC kindreds. This case report provides important information on Japanese HNPCC patients occurring endometrial cancer.
引用
收藏
页码:287 / 292
页数:6
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