Document Detail


Review article: The Lynch syndrome (hereditary nonpolyposis colorectal cancer).
MedLine Citation:
PMID:  18081655     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: The most common inherited colorectal cancer syndrome is the Lynch syndrome (HNPCC) which is characterized by the development of colorectal, endometrial, and other cancers and the presence of microsatellite instability (MSI) in tumours. The syndrome is due to a mutation in one of the mismatch repair (MMR) genes: MSH2, MLH1, MSH6 and PMS2. AIMS: To evaluate the clinical features of the Lynch syndrome and to assess the tools that are available for the identification of families with this syndrome. METHODS: A systematic literature search using PubMed and reference lists of retrieved articles was performed. RESULTS: The review provides an update of the clinical phenotype of the Lynch syndrome. Until recently, the Amsterdam criteria were the most important tool for the identification of Lynch syndrome. Nowadays, the Bethesda guidelines are more widely used. These guidelines describe all clinical conditions in which a search for MSI indicated. Both MSI-analysis as well as immunohistochemical analysis of the MMR-proteins are appropriate to identify patients with a high probability of carrying a MMR-gene mutation. CONCLUSION: All specialists that are involved in the treatment of cancer patients should know the Bethesda criteria in order to identify all families suspected of the Lynch syndrome.
Authors:
H F A Vasen
Related Documents :
12807965 - Spectrum of nsd1 mutations in sotos and weaver syndromes.
19821155 - Clinical and histomolecular endometrial tumor characterization of patients at-risk for ...
20687505 - Ligase iv syndrome.
15645695 - Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: ...
1113225 - Cerebro-hepato-renal syndrome of zellweger. a report of eight cases with comments upon ...
19533205 - Metabolic syndrome increases the risk of stroke: a 5-year follow-up study in a chinese ...
Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Alimentary pharmacology & therapeutics     Volume:  26 Suppl 2     ISSN:  1365-2036     ISO Abbreviation:  Aliment. Pharmacol. Ther.     Publication Date:  2007 Dec 
Date Detail:
Created Date:  2007-12-17     Completed Date:  2008-04-11     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8707234     Medline TA:  Aliment Pharmacol Ther     Country:  England    
Other Details:
Languages:  eng     Pagination:  113-26     Citation Subset:  IM    
Affiliation:
Department of Gastroenterology & Medical Oncology, Leiden University Medical Centre, Leiden, The Netherlands. hfavasen@stoet.nl
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Age of Onset
Colorectal Neoplasms / diagnosis,  genetics*,  therapy
Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis,  genetics*,  therapy
DNA Mismatch Repair*
Humans
Microsatellite Instability*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Review article: Detection and management of hereditary non-polyposis colorectal cancer (Lynch syndro...
Next Document:  Original article: New surgical approaches to the Klatskin tumour.