Jackson Carl-Christian, Holter Spring, Pollett Aaron, Clendenning Mark, Chou Shirley, Senter Leigha, Ramphal Raveena, Gallinger Steven, Boycott Kym
Division of General Surgery, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
Pediatr Blood Cancer. 2008 Jun;50(6):1268-70. doi: 10.1002/pbc.21514.
A 14-year-old male presented with a T4 sigmoid adenocarcinoma, <10 colonic adenomas and multiple café-au-lait macules. Family history was not suggestive of a dominant hereditary form of colorectal cancer. Evaluation of the tumor revealed abnormal immunohistochemical staining of the PMS2 protein and high frequency microsatellite instability. Germline analysis identified biallelic PMS2 missense mutations. A new cancer syndrome caused by biallelic mutations in the mismatch repair genes, including PMS2, is now emerging and is characterized by café-au-lait macules, colonic polyps and a distinctive tumor spectrum.
一名14岁男性患者,患有T4期乙状结肠腺癌,结肠腺瘤少于10个,并有多处咖啡牛奶斑。家族史未提示存在显性遗传性结直肠癌。对肿瘤的评估显示PMS2蛋白免疫组化染色异常以及高频微卫星不稳定性。胚系分析发现双等位基因PMS2错义突变。一种由错配修复基因(包括PMS2)双等位基因突变引起的新型癌症综合征正在出现,其特征为咖啡牛奶斑、结肠息肉和独特的肿瘤谱。