Centro de Investigação de Patobiologia Molecular (CIPM), Patológica Instituto Português de Oncologia de Lisboa Francisco Gentil, EPE (IPOLFG, EPE), 1099-023 Lisboa, Portugal.
Clin Genet. 2009 Sep;76(3):242-55. doi: 10.1111/j.1399-0004.2009.01241.x.
Patients presenting familial adenomatous polyposis (FAP), attenuated familial adenomatous polyposis (AFAP) or multiple colorectal adenomas (MCRAs) phenotype are clinically difficult to distinguish. We aimed to genetically characterize 107 clinically well-characterized patients with FAP-like phenotype, and stratified according to the recent guidelines for the clinical management of FAP: FAP, AFAP, MCRA (10-99 colorectal adenomas) without family history of colorectal cancer or few adenomas (FH), MCRA (10-99) with FH, MCRA (3-9) with FH. Overall, APC or MUTYH mutations were detected in 42/48 (88%), 14/20 (70%) and 10/38 (26%) of FAP, AFAP and MCRA patients, respectively. APC and MUTYH mutations accounted for 81% and 7% of FAP patients and for 30% and 40% of AFAP patients, respectively. Notably, MCRA patients did not present APC mutations. In 26% of these patients, an MUTYH mutation was identified and the detection rate increased with the number of adenomas, irrespectively of family history, being significantly higher in MCRA patients presenting more than 30 adenomas [7/12 (58%) vs 2/14 (14%), p = 0.023]. We validate the recently proposed guidelines in our patient's cohort and show that APC or MUTYH germline defects are responsible for the majority of clinically well-characterized patients with FAP and AFAP phenotype, and patients with more than 30 colorectal adenomas. The different mutation frequencies according to family history and to the number of adenomas underscore the importance of an adequate familial characterization, both clinically and by colonoscopy, in the management of FAP-like phenotypes. The phenotypes of the mutation-negative patients suggest distinct etiologies in these cases.
患者表现出家族性腺瘤性息肉病(FAP)、低危家族性腺瘤性息肉病(AFAP)或多发性结直肠腺瘤(MCRAs)表型,临床上难以区分。我们旨在对 107 例具有 FAP 样表型的临床特征明确的患者进行基因特征分析,并根据最近的 FAP 临床管理指南进行分层:FAP、AFAP、MCRA(10-99 个结直肠腺瘤)无结直肠癌家族史或腺瘤较少(FH)、MCRA(10-99)有 FH、MCRA(3-9)有 FH。总体而言,APC 或 MUTYH 突变分别在 42/48(88%)、14/20(70%)和 10/38(26%)的 FAP、AFAP 和 MCRA 患者中被检测到。APC 和 MUTYH 突变分别占 FAP 患者的 81%和 7%,占 AFAP 患者的 30%和 40%。值得注意的是,MCRA 患者未出现 APC 突变。在这些患者中的 26%中,鉴定出了 MUTYH 突变,且随着腺瘤数量的增加,突变的检出率增加,与家族史无关,在存在超过 30 个腺瘤的 MCRA 患者中,突变的检出率显著更高[7/12(58%)比 2/14(14%),p=0.023]。我们在患者队列中验证了最近提出的指南,并表明 APC 或 MUTYH 种系缺陷是大多数具有 FAP 和 AFAP 表型及具有超过 30 个结直肠腺瘤的临床特征明确的患者的主要原因。根据家族史和腺瘤数量的不同突变频率强调了在 FAP 样表型的管理中进行适当的家族特征分析的重要性,包括临床和结肠镜检查。在这些情况下,未突变患者的表型提示存在不同的病因。