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Endoscopic management of Lynch syndrome and of familial risk of colorectal cancer: European Society of Gastrointestinal Endoscopy (ESGE) Guideline.
van Leerdam, Monique E; Roos, Victorine H; van Hooft, Jeanin E; Balaguer, Francesc; Dekker, Evelien; Kaminski, Michal F; Latchford, Andrew; Neumann, Helmut; Ricciardiello, Luigi; Rupinska, Maria; Saurin, Jean-Christophe; Tanis, Pieter J; Wagner, Anja; Jover, Rodrigo; Pellisé, Maria.
Afiliação
  • van Leerdam ME; Department of Gastroenterology and Hepatology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Roos VH; Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands, Foundation for the Detection of Hereditary Tumours, Leiden, The Netherlands.
  • van Hooft JE; Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Balaguer F; Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Dekker E; Gastroenterology Department, Hospital Clínic de Barcelona, Barcelona, Spain.
  • Kaminski MF; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Institut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
  • Latchford A; Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Neumann H; Department of Cancer Prevention, The Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland.
  • Ricciardiello L; Department of Gastroenterology, Hepatology and Clinical Oncology, Medical Centre for Postgraduate Education, Warsaw, Poland.
  • Rupinska M; Department of Health Management and Health Economics, University of Oslo, Oslo, Norway.
  • Saurin JC; Polyposis Registry, St. Mark's Hospital, Harrow, United Kingdom.
  • Tanis PJ; Department of Surgery and Cancer, Imperial College London, London, United Kingdom.
  • Wagner A; Department of Medicine I, University Medical Center Mainz, Mainz, Germany.
  • Jover R; Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
  • Pellisé M; Department of Cancer Prevention, The Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland.
Endoscopy ; 51(11): 1082-1093, 2019 11.
Article em En | MEDLINE | ID: mdl-31597170
ABSTRACT
ESGE recommends that individuals with Lynch syndrome should be followed in dedicated units that practice monitoring of compliance and endoscopic performance measures.Strong recommendation, low quality evidence, level of agreement 100 %.ESGE recommends starting colonoscopy surveillance at the age of 25 years for MLH1 and MSH2 mutation carriers and at the age of 35 years for MSH6 and PMS2 mutation carriers.Strong recommendation, moderate quality evidence, level of agreement 100 %. ESGE recommends the routine use of high-definition endoscopy systems in individuals with Lynch syndrome. Strong recommendation, high quality evidence, level of agreement 100 %. ESGE suggests the use of chromoendoscopy may be of benefit in individuals with Lynch syndrome undergoing colonoscopy; however routine use must be balanced against costs, training, and practical considerations.Weak recommendation, moderate quality evidence, level of agreement 89 %.ESGE recommends definition of familial risk of colorectal cancer as the presence of at least two first-degree relatives with colorectal cancer or at least one first-degree relative with colorectal cancer before the age of 50 years.Strong recommendation, moderate quality evidence, level of agreement 92 %.ESGE recommends colonoscopy surveillance in first-degree relatives of colorectal cancer patients in families that fulfill the definition of familial risk of colorectal cancer.Strong recommendation, moderate quality evidence, level of agreement 100 %.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sociedades Médicas / Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose / Colonoscopia / Gerenciamento Clínico / Predisposição Genética para Doença Tipo de estudo: Etiology_studies / Guideline / Risk_factors_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sociedades Médicas / Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose / Colonoscopia / Gerenciamento Clínico / Predisposição Genética para Doença Tipo de estudo: Etiology_studies / Guideline / Risk_factors_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article