Surveillance in Lynch Syndrome
- 1 September 2005
- journal article
- review article
- Published by Springer Nature in Familial Cancer
- Vol. 4 (3) , 267-271
- https://doi.org/10.1007/s10689-005-1475-x
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.Keywords
This publication has 43 references indexed in Scilit:
- A Randomized Trial of Aspirin to Prevent Colorectal AdenomasNew England Journal of Medicine, 2003
- A Randomized Trial of Aspirin to Prevent Colorectal Adenomas in Patients with Previous Colorectal CancerNew England Journal of Medicine, 2003
- Non-Hodgkin's Lymphoma in a Patient with Probable Hereditary Nonpolyposis Colon CancerDiseases of the Colon & Rectum, 2002
- Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigreeJournal of Medical Genetics, 2001
- Predictive genetic testing for hereditary non-polyposis colorectal cancer: Uptake and long-term satisfactionInternational Journal of Cancer, 2000
- In a resource-poor country, mutation identification has the potential to reduce the cost of family management for hereditary nonpolyposis colorectal cancerDiseases of the Colon & Rectum, 1998
- Hereditary Nonpolyposis Colorectal Cancer Families Not Complying with the Amsterdam Criteria Show Extremely Low Frequency of Mismatch-Repair-Gene MutationsAmerican Journal of Human Genetics, 1997
- Life‐time risk of different cancers in hereditary non‐polyposis colorectal cancer (hnpcc) syndromeInternational Journal of Cancer, 1995
- Tumor spectrum in cancer family syndrome (hereditary nonpolyposis colorectal cancer)Cancer, 1991
- The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)Diseases of the Colon & Rectum, 1991