Familial colorectal cancer syndromes: an overview of clinical management.
Expert Rev Gastroenterol Hepatol. 2015 Jun; 9(6):757-64.ER

Abstract

Familial colorectal cancer syndromes pose a complex challenge to the treating clinician. Once a syndrome is recognized, genetic testing is often required to confirm the clinical suspicion. Management from that point is usually based on disease-specific guideline recommendations targeting risk reduction for the patient and their relatives through surgery, surveillance and chemoprophylaxis. The aim of this paper is to provide an up-to-date summary of the most common familial syndromes and their medical and surgical management, with specific emphasis on evidence-based interventions that improve patient outcome, and to present the information in a manner that is easily readable and clinically relevant to the treating clinician.

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Authors+Show Affiliations

Sammour T
Colorectal Surgery Unit, Department of Surgery, The Royal Melbourne Hospital, Melbourne, VIC, Australia.
Hayes IP
No affiliation info available
Hill AG
No affiliation info available
Macrae FA
No affiliation info available
Winter DC
No affiliation info available

MeSH

Adenomatous Polyposis ColiBiomarkers, TumorColorectal Neoplasms, Hereditary NonpolyposisGenetic Predisposition to DiseaseGenetic TestingHeredityHumansIntestinal PolyposisNeoplastic Syndromes, HereditaryPedigreePeutz-Jeghers SyndromePhenotypePredictive Value of TestsTreatment Outcome

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

25779305