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体质性错配修复缺陷综合征的胃肠道表现:从单个腺瘤到息肉样表型及早期癌症。

The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer.

作者信息

Levi Z, Kariv R, Barnes-Kedar I, Goldberg Y, Half E, Morgentern S, Eli B, Baris H N, Vilkin A, Belfer R G, Niv Y, Elhasid R, Dvir R, Abu-Freha N, Cohen S

机构信息

The Early Detection and High Risk GI Cancer Service, the Gastroenterology Division, Rabin Medical Center, Petach Tikva, Israel.

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Clin Genet. 2015 Nov;88(5):474-8. doi: 10.1111/cge.12518. Epub 2014 Nov 10.

DOI:10.1111/cge.12518
PMID:25307252
Abstract

Data on the clinical presentation of constitutional mismatch repair deficiency syndrome (CMMRD) is accumulating. However, as the extraintestinal manifestations are often fatal and occur at early age, data on the systematic evaluation of the gastrointestinal tract is scarce. Here we describe 11 subjects with verified biallelic carriage and who underwent colonoscopy, upper endoscopy and small bowel evaluation. Five subjects were symptomatic and in six subjects the findings were screen detected. Two subjects had colorectal cancer and few adenomatous polyps (19, 20 years), three subjects had polyposis-like phenotype (13, 14, 16 years), four subjects had few adenomatous polyps (8, 12-14 years) and two subjects had no polyps (both at age 6). Of the three subjects in the polyposis-like group, two subjects had already developed high-grade dysplasia or cancer and one subject had atypical juvenile polyps suggesting juvenile polyposis. Three out of the five subjects that underwent repeated exams had significant findings during short interval. The gastrointestinal manifestations of CMMRD are highly dependent upon age of examination and highly variable. The polyps may also resemble juvenile polyposis. Intensive surveillance according to current guidelines is mandatory.

摘要

关于体质性错配修复缺陷综合征(CMMRD)临床表现的数据正在不断积累。然而,由于肠道外表现往往是致命的且发生在幼年时期,关于胃肠道系统评估的数据很少。在此,我们描述了11名经证实携带双等位基因且接受了结肠镜检查、上消化道内镜检查和小肠评估的受试者。5名受试者有症状,6名受试者的检查结果是筛查发现的。2名受试者患有结直肠癌且有少量腺瘤性息肉(19、20岁),3名受试者有息肉样表型(13、14、16岁),4名受试者有少量腺瘤性息肉(8、12 - 14岁),2名受试者没有息肉(均为6岁)。在息肉样组的3名受试者中,2名受试者已经发展为高级别发育异常或癌症,1名受试者有非典型幼年息肉提示幼年性息肉病。在接受重复检查的5名受试者中,有3名在短时间内有显著发现。CMMRD的胃肠道表现高度依赖于检查年龄且变化很大。这些息肉也可能类似于幼年性息肉病。根据现行指南进行强化监测是必要的。

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