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Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus
Advanced esophageal adenocarcinomas arising from Barrett esophagus (BE) are tumors with an increasing incidence and poor prognosis. The aim of endoscopic surveillance of BE is to detect dysplasia, particularly high-grade dysplasia and intramucosal cancers that can subsequently be treated endoscopica...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Gastrointestinal Endoscopy
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928491/ https://www.ncbi.nlm.nih.gov/pubmed/24570883 http://dx.doi.org/10.5946/ce.2014.47.1.47 |
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author | Espino, Alberto Cirocco, Maria DaCosta, Ralph Marcon, Norman |
author_facet | Espino, Alberto Cirocco, Maria DaCosta, Ralph Marcon, Norman |
author_sort | Espino, Alberto |
collection | PubMed |
description | Advanced esophageal adenocarcinomas arising from Barrett esophagus (BE) are tumors with an increasing incidence and poor prognosis. The aim of endoscopic surveillance of BE is to detect dysplasia, particularly high-grade dysplasia and intramucosal cancers that can subsequently be treated endoscopically before progression to invasive cancer with lymph node metastases. Current surveillance practice standards require the collection of random 4-quadrant biopsy specimens over every 1 to 2 cm of BE (Seattle protocol) to detect dysplasia with the assistance of white light endoscopy, in addition to performing targeted biopsies of recognizable lesions. This approach is labor-intensive but should currently be considered state of the art. Chromoendoscopy, virtual chromoendoscopy (e.g., narrow band imaging), and confocal laser endomicroscopy, in addition to high-definition standard endoscopy, might increase the diagnostic yield for the detection of dysplastic lesions. Until these modalities have been demonstrated to enhance efficiency or cost effectiveness, the standard protocol will remain careful examination using conventional off the shelf high-resolution endoscopes, combined with as longer inspection time which is associated with increased detection of dysplasia. |
format | Online Article Text |
id | pubmed-3928491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Society of Gastrointestinal Endoscopy |
record_format | MEDLINE/PubMed |
spelling | pubmed-39284912014-02-25 Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus Espino, Alberto Cirocco, Maria DaCosta, Ralph Marcon, Norman Clin Endosc Focused Review Series: Endoscopic and Molecular Imaging of Premalignant GI Lesions, Part II Advanced esophageal adenocarcinomas arising from Barrett esophagus (BE) are tumors with an increasing incidence and poor prognosis. The aim of endoscopic surveillance of BE is to detect dysplasia, particularly high-grade dysplasia and intramucosal cancers that can subsequently be treated endoscopically before progression to invasive cancer with lymph node metastases. Current surveillance practice standards require the collection of random 4-quadrant biopsy specimens over every 1 to 2 cm of BE (Seattle protocol) to detect dysplasia with the assistance of white light endoscopy, in addition to performing targeted biopsies of recognizable lesions. This approach is labor-intensive but should currently be considered state of the art. Chromoendoscopy, virtual chromoendoscopy (e.g., narrow band imaging), and confocal laser endomicroscopy, in addition to high-definition standard endoscopy, might increase the diagnostic yield for the detection of dysplastic lesions. Until these modalities have been demonstrated to enhance efficiency or cost effectiveness, the standard protocol will remain careful examination using conventional off the shelf high-resolution endoscopes, combined with as longer inspection time which is associated with increased detection of dysplasia. The Korean Society of Gastrointestinal Endoscopy 2014-01 2014-01-24 /pmc/articles/PMC3928491/ /pubmed/24570883 http://dx.doi.org/10.5946/ce.2014.47.1.47 Text en Copyright © 2014 Korean Society of Gastrointestinal Endoscopy http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Focused Review Series: Endoscopic and Molecular Imaging of Premalignant GI Lesions, Part II Espino, Alberto Cirocco, Maria DaCosta, Ralph Marcon, Norman Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus |
title | Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus |
title_full | Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus |
title_fullStr | Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus |
title_full_unstemmed | Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus |
title_short | Advanced Imaging Technologies for the Detection of Dysplasia and Early Cancer in Barrett Esophagus |
title_sort | advanced imaging technologies for the detection of dysplasia and early cancer in barrett esophagus |
topic | Focused Review Series: Endoscopic and Molecular Imaging of Premalignant GI Lesions, Part II |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928491/ https://www.ncbi.nlm.nih.gov/pubmed/24570883 http://dx.doi.org/10.5946/ce.2014.47.1.47 |
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