Hyperplastic Polyposis Syndrome Identified with a BRAF Mutation

被引:3
作者
Ahn, Hyung Su [1 ]
Hong, Su Jin [1 ]
Kim, Hee Kyung [2 ]
Yoo, Hee Yong [1 ]
Kim, Hwa Jong [1 ]
Ko, Bong Min [1 ]
Lee, Moon Sung [1 ]
机构
[1] Soonchunhyang Univ, Coll Med, Dept Internal Med, Ctr Digest Dis, Puchon 420767, South Korea
[2] Soonchunhyang Univ, Coll Med, Dept Pathol, Puchon 420767, South Korea
关键词
Hyperplastic polyposis syndrome; BRAF; COLORECTAL-CANCER; SERRATED ADENOMAS; KRAS MUTATIONS; MICROSATELLITE INSTABILITY; COLON; PATHWAYS; RISK; CLASSIFICATION; METHYLATION; GENETICS;
D O I
10.5009/gnl.2012.6.2.280
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hyperplastic polyposis syndrome (HPS) is a rare condition characterized by the presence of numerous hyperplastic polyps (HPs) in the colon and rectum. Patients with HPS have an increased risk of colorectal cancer. This link is associated with gene mutations, especially B type Raf kinase (BRAF). However, a case of HPS associated with gene mutations has seldom been reported in Korea. Here, we describe a case of HPS in which a BRAF mutation was present in a 34-year-old woman. She had more than 110 HPs in the stomach and colorectum, which we removed. All of the polyps were diagnosed histologically as HPs, and no adenomatous or malignant changes were noted. We performed a BRAF and K-ras mutation analysis as well as a microsatellite analysis on the resected colon polyps. BRAF mutations were found in the resected colon polyps, but there was no evidence of K-RAS mutation or microsatellite instability. (Gut Liver 2012;6:280-283)
引用
收藏
页码:280 / 283
页数:4
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