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定义林奇综合征中的腺瘤负荷。

Defining the adenoma burden in lynch syndrome.

作者信息

Kalady Matthew F, Kravochuck Sara E, Heald Brandie, Burke Carol A, Church James M

机构信息

Department of Colorectal Surgery, Sanford R. Weiss, M.D., Center for Hereditary Colorectal Neoplasia, Digestive Diseases Institute, Cleveland Clinic, Cleveland, Ohio.

出版信息

Dis Colon Rectum. 2015 Apr;58(4):388-92. doi: 10.1097/DCR.0000000000000333.

Abstract

BACKGROUND

Patients with 10 or more lifetime adenomas are candidates for genetic counseling and testing for polyposis syndromes. Lynch syndrome falls under the umbrella of hereditary nonpolyposis colorectal cancer, and it is assumed that patients with Lynch syndrome do not develop multiple adenomas.

OBJECTIVE

The objective of this study was to document the number of adenomas in patients with Lynch syndrome.

DESIGN

This was a retrospective review of clinical, colonoscopy, and pathology records of patients with Lynch syndrome in a prospectively maintained hereditary colorectal cancer database.

SETTINGS

The study was conducted at a single-institution tertiary care center with specialized practice in hereditary colorectal cancer syndromes.

PATIENTS

We included 263 patients with a germline mutation in 1 of the 4 DNA mismatch repair genes.

INTERVENTIONS

Colonoscopy and polypectomy were the study interventions.

MAIN OUTCOME MEASURES

The lifetime cumulative number of colorectal adenomas and their characteristics were measured.

RESULTS

A total of 107 of the 263 patients had 1 or more adenomas. Sixty-one patients had 1 adenoma, 29 (11%) had 2 to 5 adenomas, 6 (2%) had 6 to 9 adenomas, and 11 patients (4%) had 10 or more cumulative adenomas. The maximum number of synchronous adenomas in any individual was 22, and the maximum number of cumulative adenomas in any individual was 24. Twenty-four of the 107 patients with adenomas underwent a total colectomy or proctocolectomy and were excluded from long-term follow-up. In the remaining 83 patients with adenomas, 426 colonoscopies were performed. A total of 220 (54%) were normal or had hyperplastic polyps; 313 adenomas were found in 206 examinations (46%), and 123 (39%) of the adenomas were advanced.

LIMITATIONS

There was variability in the interval of colonoscopy surveillance. Some patients had a variant of unknown significance and were separated from those with a deleterious mutation.

CONCLUSIONS

Although 10 or more adenomas prompt testing for polyposis syndromes, Lynch syndrome should also be considered in the differential diagnosis.

摘要

背景

一生中患腺瘤10个或更多的患者是进行息肉病综合征遗传咨询和检测的对象。林奇综合征属于遗传性非息肉病性结直肠癌范畴,一般认为林奇综合征患者不会发生多个腺瘤。

目的

本研究的目的是记录林奇综合征患者的腺瘤数量。

设计

这是一项对前瞻性维护的遗传性结直肠癌数据库中林奇综合征患者的临床、结肠镜检查和病理记录进行的回顾性研究。

地点

该研究在一家对遗传性结直肠癌综合征有专门诊疗的单机构三级医疗中心进行。

患者

我们纳入了263名在4个DNA错配修复基因中的1个基因存在种系突变的患者。

干预措施

结肠镜检查和息肉切除术为研究干预措施。

主要观察指标

测量结直肠腺瘤的终生累积数量及其特征。

结果

263名患者中共有107名有1个或更多腺瘤。61名患者有1个腺瘤,29名(11%)有2至5个腺瘤,6名(2%)有6至9个腺瘤,11名患者(4%)有10个或更多累积腺瘤。任何个体同步腺瘤的最大数量为22个,任何个体累积腺瘤的最大数量为24个。107名有腺瘤的患者中有24名接受了全结肠切除术或直肠结肠切除术,并被排除在长期随访之外。在其余83名有腺瘤的患者中,进行了426次结肠镜检查。共有220次(54%)检查结果正常或有增生性息肉;在206次检查(46%)中发现了313个腺瘤,其中123个(39%)腺瘤为进展期。

局限性

结肠镜监测间隔存在差异。一些患者有意义不明的变异,与有有害突变的患者分开。

结论

虽然10个或更多腺瘤提示进行息肉病综合征检测,但在鉴别诊断中也应考虑林奇综合征。

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