Ahn Do Hee, Rho Jung Hee, Tchah Hann, Jeon In-Sang
Department of Pediatrics, Graduate School of Medicine, Gachon University, Incheon, Korea.
Korean J Pediatr. 2016 Jan;59(1):40-2. doi: 10.3345/kjp.2016.59.1.40. Epub 2016 Jan 22.
Lynch syndrome is the most common inherited colon cancer syndrome. Patients with Lynch syndrome develop a range of cancers including colorectal cancer (CRC) and carry a mutation on one of the mismatched repair (MMR) genes. Although CRC usually occurs after the fourth decade in patients with Lynch syndrome harboring a heterozygous MMR gene mutation, it can occur in children with Lynch syndrome who have a compound heterozygous or homozygous MMR gene mutation. We report a case of CRC in a 13-year-old patient with Lynch syndrome and congenital heart disease. This patient had a heterozygous mutation in MLH1 (an MMR gene), but no compound MMR gene defects, and a K-RAS somatic mutation in the cancer cells.
林奇综合征是最常见的遗传性结肠癌综合征。林奇综合征患者会罹患一系列癌症,包括结直肠癌(CRC),且其错配修复(MMR)基因之一存在突变。虽然携带杂合MMR基因突变的林奇综合征患者的结直肠癌通常在40岁以后发生,但在具有复合杂合或纯合MMR基因突变的林奇综合征儿童中也可能发生。我们报告一例患有林奇综合征和先天性心脏病的13岁患者发生结直肠癌的病例。该患者的MLH1(一种MMR基因)存在杂合突变,但不存在复合MMR基因缺陷,且癌细胞存在K-RAS体细胞突变。