| Literature DB >> 26893603 |
Do Hee Ahn1, Jung Hee Rho1, Hann Tchah1, In-Sang Jeon1.
Abstract
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.Entities:
Keywords: Colorectal neoplasms; Lynch syndrome; Mismatched repair genes
Year: 2016 PMID: 26893603 PMCID: PMC4753199 DOI: 10.3345/kjp.2016.59.1.40
Source DB: PubMed Journal: Korean J Pediatr ISSN: 1738-1061