Your browser doesn't support javascript.
loading
Barrett oesophagus.
Peters, Yonne; Al-Kaabi, Ali; Shaheen, Nicholas J; Chak, Amitabh; Blum, Andrew; Souza, Rhonda F; Di Pietro, Massimiliano; Iyer, Prasad G; Pech, Oliver; Fitzgerald, Rebecca C; Siersema, Peter D.
Affiliation
  • Peters Y; Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, Netherlands.
  • Al-Kaabi A; Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, Netherlands.
  • Shaheen NJ; Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Chak A; Division of Gastroenterology and Liver Diseases, Case Western Reserve University, Cleveland, OH, USA.
  • Blum A; Division of Gastroenterology and Liver Diseases, Case Western Reserve University, Cleveland, OH, USA.
  • Souza RF; Department of Medicine and the Center for Esophageal Diseases, Baylor University Medical Center at Dallas and the Center for Esophageal Research, Baylor Scott and White Research Institute, Dallas, TX, USA.
  • Di Pietro M; Medical Research Council Cancer Unit, University of Cambridge, Cambridge, UK.
  • Iyer PG; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
  • Pech O; Department of Gastroenterology, St John of God Hospital, Regensburg, Germany.
  • Fitzgerald RC; Medical Research Council Cancer Unit, University of Cambridge, Cambridge, UK.
  • Siersema PD; Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, Netherlands. peter.siersema@radboudumc.nl.
Nat Rev Dis Primers ; 5(1): 35, 2019 05 23.
Article de En | MEDLINE | ID: mdl-31123267
Barrett oesophagus (BE), the only known histological precursor of oesophageal adenocarcinoma (EAC), is a condition in which the squamous epithelium of the oesophagus is replaced by columnar epithelium as an adaptive response to gastro-oesophageal reflux. EAC has one of the fastest rising incidences of cancers in Western countries and has a dismal prognosis. BE is usually detected during endoscopic examination, and diagnosis is confirmed by the histological presence of intestinal metaplasia. Advances in genomics and transcriptomics have improved our understanding of the pathogenesis and malignant progression of intestinal metaplasia. As the majority of EAC cases are diagnosed in individuals without a known history of BE, screening for BE could potentially decrease disease-related mortality. Owing to the pre-malignant nature of BE, endoscopic surveillance of patients with BE is imperative for early detection and treatment of dysplasia to prevent further progression to invasive EAC. Developments in endoscopic therapy have resulted in a major shift in the treatment of patients with BE who have dysplasia or early EAC, from surgical resection to endoscopic resection and ablation. In addition to symptom control by optimization of lifestyle and pharmacological therapy with proton pump inhibitors, chemopreventive strategies based on NSAIDs and statins are currently being investigated for BE management.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Oesophage de Barrett Type d'étude: Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limites: Humans Langue: En Journal: Nat Rev Dis Primers Année: 2019 Type de document: Article Pays d'affiliation: Pays-Bas Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Oesophage de Barrett Type d'étude: Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limites: Humans Langue: En Journal: Nat Rev Dis Primers Année: 2019 Type de document: Article Pays d'affiliation: Pays-Bas Pays de publication: Royaume-Uni