• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

林奇综合征的监测

Surveillance in Lynch syndrome.

作者信息

Mecklin Jukka-Pekka, Järvinen Heikki J

机构信息

Department of Surgery, Jyväskylä Central Hospital, 40620, Jyväskylä, Finland.

出版信息

Fam Cancer. 2005;4(3):267-71. doi: 10.1007/s10689-005-1475-x.

DOI:10.1007/s10689-005-1475-x
PMID:16136388
Abstract

The major aim of surveillance in Lynch syndrome is to diagnose malignant or premalignant lesions at the asymptomatic stage by regular checkups, particularly in the large bowel. Therefore, screening for colorectal adenomas and carcinomas by regular colonoscopies is the main topic of the present review. However, it should be remembered, that primary prevention - whether through the use of chemoprevention or the promotion of a healthy life-style may form a significant part of such surveillance in the future. Observational studies indicate that the adenoma carcinoma sequence is the main pathway in the development of colorectal cancer in Lynch syndrome. A colonoscopy every 1-3 years starting at age 20 to 25 years and the removal of observed adenomas is recommended for individuals known to have Lynch syndrome associated mutations. The incidence of colorectal cancer in family branches screened this way is lower than that in past unscreened generations. The screening of other malignancies associated with Lynch syndrome is more complex. Screening for endometrial cancer has recommended previously, but no benefits have been shown in recent studies. The value of screening for other extracolonic cancers remains also uncertain.

摘要

林奇综合征监测的主要目的是通过定期检查在无症状阶段诊断恶性或癌前病变,尤其是在大肠。因此,通过定期结肠镜检查筛查结直肠腺瘤和癌是本综述的主要主题。然而,应该记住,一级预防——无论是通过化学预防还是促进健康的生活方式——在未来可能会成为这种监测的重要组成部分。观察性研究表明,腺瘤-癌序列是林奇综合征中结直肠癌发生的主要途径。对于已知有林奇综合征相关突变的个体,建议从20至25岁开始每1至3年进行一次结肠镜检查,并切除观察到的腺瘤。以这种方式筛查的家族分支中结直肠癌的发病率低于过去未筛查的几代人。与林奇综合征相关的其他恶性肿瘤的筛查更为复杂。以前曾建议筛查子宫内膜癌,但最近的研究未显示出益处。筛查其他结肠外癌症的价值也仍然不确定。

相似文献

1
Surveillance in Lynch syndrome.林奇综合征的监测
Fam Cancer. 2005;4(3):267-71. doi: 10.1007/s10689-005-1475-x.
2
Colonoscopy screening compliance and outcomes in patients with Lynch syndrome.林奇综合征患者的结肠镜筛查依从性及结果
Colorectal Dis. 2015 Jan;17(1):38-46. doi: 10.1111/codi.12778.
3
Colorectal adenomas in the Lynch syndromes. Results of a colonoscopy screening program.林奇综合征中的结直肠腺瘤。结肠镜筛查项目的结果。
Gastroenterology. 1990 May;98(5 Pt 1):1117-22. doi: 10.1016/0016-5085(90)90323-s.
4
Development of colorectal tumors in colonoscopic surveillance in Lynch syndrome.林奇综合征结肠镜监测中结直肠肿瘤的发生
Gastroenterology. 2007 Oct;133(4):1093-8. doi: 10.1053/j.gastro.2007.08.019. Epub 2007 Aug 14.
5
Surveillance colonoscopy practice in Lynch syndrome in the Netherlands: A nationwide survey.荷兰林奇综合征的监测结肠镜检查实践:一项全国性调查。
World J Gastroenterol. 2007 Sep 14;13(34):4658-9. doi: 10.3748/wjg.v13.i34.4659.
6
Prospective results of surveillance colonoscopy in dominant familial colorectal cancer with and without Lynch syndrome.伴有和不伴有林奇综合征的显性家族性结直肠癌监测结肠镜检查的前瞻性结果
Gastroenterology. 2006 Jun;130(7):1995-2000. doi: 10.1053/j.gastro.2006.03.018.
7
Surveillance colonoscopy in individuals at risk for hereditary nonpolyposis colorectal cancer: an evidence-based review.遗传性非息肉病性结直肠癌高危个体的监测结肠镜检查:一项基于证据的综述。
Dis Colon Rectum. 2006 Jan;49(1):80-93; discussion 94-5. doi: 10.1007/s10350-005-0228-0.
8
Surveillance in Lynch syndrome: how aggressive?林奇综合征的监测:应采取何种积极程度?
Am J Gastroenterol. 1994 Nov;89(11):1978-80.
9
[Early diagnosis of colorectal carcinoma in the familial carcinoma syndrome (Lynch I and II)].
Bratisl Lek Listy. 1993 Jun;94(6):302-7.
10
Colonoscopy: a review of its yield for cancers and adenomas by indication.结肠镜检查:按适应证对其癌症和腺瘤检出率的综述。
Am J Gastroenterol. 1995 Mar;90(3):353-65.

引用本文的文献

1
Association of Mismatch Repair Mutation With Age at Cancer Onset in Lynch Syndrome: Implications for Stratified Surveillance Strategies.错配修复基因突变与林奇综合征发病年龄的关联:对分层监测策略的影响。
JAMA Oncol. 2017 Dec 1;3(12):1702-1706. doi: 10.1001/jamaoncol.2017.0619.
2
MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome.阿根廷疑似林奇综合征家族中的MLH1基因Ile219Val多态性
Front Oncol. 2016 Aug 24;6:189. doi: 10.3389/fonc.2016.00189. eCollection 2016.
3
Muir-Torre syndrome: case report and molecular characterization.

本文引用的文献

1
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.MSH6 突变导致的遗传性非息肉病性结直肠癌的癌症风险:对咨询和监测的影响。
Gastroenterology. 2004 Jul;127(1):17-25. doi: 10.1053/j.gastro.2004.03.068.
2
Spectrum of genetic alterations in Muir-Torre syndrome is the same as in HNPCC.穆尔-托雷综合征的基因改变谱与遗传性非息肉病性结直肠癌相同。
Am J Med Genet A. 2004 Mar 15;125A(3):318-9. doi: 10.1002/ajmg.a.20523.
3
Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer.
穆尔-托雷综合征:病例报告及分子特征分析
Sao Paulo Med J. 2014;132(1):61-4. doi: 10.1590/1516-3180.2014.1321634.
4
Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.林奇综合征和家族性结直肠癌 X 型的独特基因表达特征。
PLoS One. 2013 Aug 12;8(8):e71755. doi: 10.1371/journal.pone.0071755. eCollection 2013.
5
Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutation.林奇综合征基因突变患者的结直肠癌筛查用磁共振结肠成像术
Fam Cancer. 2010 Dec;9(4):555-61. doi: 10.1007/s10689-010-9350-9.
6
MUTYH Associated Polyposis (MAP).MUTYH 相关息肉病(MAP)。
Curr Genomics. 2008 Sep;9(6):420-35. doi: 10.2174/138920208785699562.
7
TGF-beta signaling alterations and susceptibility to colorectal cancer.转化生长因子-β信号通路改变与结直肠癌易感性
Hum Mol Genet. 2007 Apr 15;16 Spec No 1(SPEC):R14-20. doi: 10.1093/hmg/ddl486.
8
The management of families affected by hereditary non-polyposis colorectal cancer (HNPCC).遗传性非息肉病性结直肠癌(HNPCC)相关家庭的管理
Fam Cancer. 2007;6(1):13-9. doi: 10.1007/s10689-006-9000-4.
遗传性非息肉病性结直肠癌家族中高危个体的基因检测。
Br J Cancer. 2004 Feb 23;90(4):882-7. doi: 10.1038/sj.bjc.6601529.
4
Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect.错配修复基因缺陷所致结直肠癌外科治疗中的决策分析
Gut. 2003 Dec;52(12):1752-5. doi: 10.1136/gut.52.12.1752.
5
Altered expression of MLH1, MSH2, and MSH6 in predisposition to hereditary nonpolyposis colorectal cancer.MLH1、MSH2和MSH6的表达改变与遗传性非息肉病性结直肠癌的易感性相关。
J Clin Oncol. 2003 Oct 1;21(19):3629-37. doi: 10.1200/JCO.2003.03.181.
6
Prostate cancer is part of the hereditary non-polyposis colorectal cancer (HNPCC) tumor spectrum.前列腺癌是遗传性非息肉病性结直肠癌(HNPCC)肿瘤谱的一部分。
Am J Med Genet A. 2003 Aug 30;121A(2):159-62. doi: 10.1002/ajmg.a.20106.
7
Practice parameters for the treatment of patients with dominantly inherited colorectal cancer (familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer).遗传性结直肠癌(家族性腺瘤性息肉病和遗传性非息肉病性结直肠癌)患者治疗的实践参数
Dis Colon Rectum. 2003 Aug;46(8):1001-12. doi: 10.1007/s10350-004-7273-y.
8
Daily soluble aspirin and prevention of colorectal adenoma recurrence: one-year results of the APACC trial.每日服用可溶性阿司匹林与预防结直肠腺瘤复发:APACC试验的一年结果
Gastroenterology. 2003 Aug;125(2):328-36. doi: 10.1016/s0016-5085(03)00887-4.
9
Preventive surgery for colon cancer in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer syndrome.家族性腺瘤性息肉病和遗传性非息肉病性结直肠癌综合征中结肠癌的预防性手术。
Langenbecks Arch Surg. 2003 Mar;388(1):9-16. doi: 10.1007/s00423-003-0364-8. Epub 2003 Mar 27.
10
Hereditary colorectal cancer.遗传性结直肠癌
N Engl J Med. 2003 Mar 6;348(10):919-32. doi: 10.1056/NEJMra012242.