ACG clinical guideline: genetic testing and management of hereditary gastrointestinal cancer syndromes

S Syngal, RE Brand, JM Church… - Official journal of the …, 2015 - journals.lww.com
This guideline presents recommendations for the management of patients with hereditary
gastrointestinal cancer syndromes. The initial assessment is the collection of a family history …

Hereditary colorectal polyposis and cancer syndromes: a primer on diagnosis and management

P Kanth, J Grimmett, M Champine, R Burt… - Official journal of the …, 2017 - journals.lww.com
Colorectal cancer (CRC) is the fourth most common cancer amongst men and women.
Between 3 and 6% of all CRCs are attributed to well-defined inherited syndromes, including …

Endoscopic management of polyposis syndromes: European Society of Gastrointestinal Endoscopy (ESGE) guideline

ME van Leerdam, VH Roos, JE van Hooft… - …, 2019 - thieme-connect.com
ESGE recommends that individuals with hereditary gastrointestinal polyposis syndromes
should be surveilled in dedicated units that provide monitoring of compliance and …

Aspirin in the chemoprevention of colorectal neoplasia: an overview

AT Chan, N Arber, J Burn, WK Chia, P Elwood… - Cancer prevention …, 2012 - AACR
Considerable evidence supports the effectiveness of aspirin for chemoprevention of
colorectal cancer (CRC) in addition to its well-established benefits in the prevention of …

Effect of sulindac and erlotinib vs placebo on duodenal neoplasia in familial adenomatous polyposis: a randomized clinical trial

NJ Samadder, DW Neklason, KM Boucher, KR Byrne… - Jama, 2016 - jamanetwork.com
Importance Patients with familial adenomatous polyposis (FAP) are at markedly increased
risk for duodenal polyps and cancer. Surgical and endoscopic management of duodenal …

Familial colon cancer syndromes: an update of a rapidly evolving field

SG Patel, DJ Ahnen - Current gastroenterology reports, 2012 - Springer
Colorectal cancer (CRC) is a major cause of morbidity and mortality in the world. Up to 30%
of CRCs have evidence of a familial component, and about 5% are thought to be due to well …

Management of familial adenomatous polyposis in children and adolescents: position paper from the ESPGHAN Polyposis Working Group

W Hyer, S Cohen, T Attard, V Vila-Miravet… - Journal of pediatric …, 2019 - journals.lww.com
Familial adenomatous polyposis (FAP) is a well-described inherited syndrome,
characterized by the development of hundreds to thousands of adenomas in the colorectum …

Systematic review of the impact of registration and screening on colorectal cancer incidence and mortality in familial adenomatous polyposis and Lynch syndrome

P Barrow, M Khan, F Lalloo, DG Evans… - Journal of British …, 2013 - academic.oup.com
Abstract Background The British Society of Gastroenterology recommends that all familial
adenomatous polyposis (FAP) and Lynch syndrome (LS) families are screened in the …

Gastric adenocarcinoma and proximal polyposis of the stomach: diagnosis and clinical perspectives

U Rudloff - Clinical and experimental gastroenterology, 2018 - Taylor & Francis
Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) is a recently
described, rare gastric polyposis syndrome. It is characterized by extensive involvement of …

American Society for Gastrointestinal Endoscopy guideline on the role of endoscopy in familial adenomatous polyposis syndromes

J Yang, SR Gurudu, C Koptiuch, D Agrawal… - Gastrointestinal …, 2020 - Elsevier
Familial adenomatous polyposis (FAP) syndrome is a complex entity, which includes FAP,
attenuated FAP, and MUTYH-associated polyposis. These patients are at significant risk for …