Holinski-Feder E, Morak M
Medizinisch Genetisches Zentrum München.
Dtsch Med Wochenschr. 2008 Aug;133(33):1690-5. doi: 10.1055/s-0028-1082788.
Familial clustering is found in 20-25% of all cases with colorectal cancer (CRC), 4-5% revealing autosomal dominant inheritance. Hereditary CRC develops from adenomatous, hyperplastic hamartomatous juvenile lesions. Hereditory nonpolyposis colorectal cancer includes two genetically different tumor entities, those with and without microsatellite instability in the corresponding tumors. Those with such instability and with germ-line mutation in DNA mismatch repair genes (Lynch syndrome) have additional neoplasms, an earlier age at onset and a higher risk for syn- and metachronous cancers.
20%-25%的结直肠癌(CRC)病例存在家族聚集性,4%-5%显示为常染色体显性遗传。遗传性CRC由腺瘤性、增生性错构瘤性幼年病变发展而来。遗传性非息肉病性结直肠癌包括两种基因不同的肿瘤实体,即相应肿瘤中存在和不存在微卫星不稳定性的实体。那些具有这种不稳定性且DNA错配修复基因发生种系突变的患者(林奇综合征)会有额外的肿瘤、发病年龄更早且同时性和异时性癌症风险更高。