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Diffuse endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (with video)

Background  Low grade dysplasia (LGD) in Barrett’s esophagus (BE) has generally been considered as undetectable endoscopically. Aim  To describe a phenotype which consists of diffuse, endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (DEVLB), with often subtle but visi...

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Autores principales: Tsoi, Edward H., Fehily, Sasha, Williams, Richard, Desmond, Paul, Taylor, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: © Georg Thieme Verlag KG 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904234/
https://www.ncbi.nlm.nih.gov/pubmed/31828211
http://dx.doi.org/10.1055/a-1031-9327
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author Tsoi, Edward H.
Fehily, Sasha
Williams, Richard
Desmond, Paul
Taylor, Andrew
author_facet Tsoi, Edward H.
Fehily, Sasha
Williams, Richard
Desmond, Paul
Taylor, Andrew
author_sort Tsoi, Edward H.
collection PubMed
description Background  Low grade dysplasia (LGD) in Barrett’s esophagus (BE) has generally been considered as undetectable endoscopically. Aim  To describe a phenotype which consists of diffuse, endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (DEVLB), with often subtle but visible endoscopic changes seen with high definition white light (HDWL) and narrow-band imaging (NBI). Method  A systematic search of a prospectively collected database for patients satisfying predefined criteria for DEVLB and a review of endoscopic and histological features of biopsies and endoscopic mucosal resection (EMR) specimens. Results  Out of a total of 419 patients referred to our expert center for assessment of dysplastic Barrett’s esophagus during the period January 2009 to March 2018, there were 7 patients (1.7 %) who satisfied the criteria defined for DEVLB, identified on their initial assessment endoscopy. All patients were treated by EMR of visible abnormal mucosa during their assessment endoscopy at our tertiary referral center. There was a total of 47 EMR specimens obtained, with a median of 6 (IQR 5–9) EMR resection pieces per patient, of which 36 (77 %) contained LGD, 8 (17 %) high grade dysplasia (HGD), 2 (4 %) non-dysplastic Barrett’s esophagus (NDBE), and 1 (2 %) contained early esophageal adenocarcinoma (EAC). Conclusion  DEVLB is a distinct phenotype seen in a small but significant proportion of individuals with dysplastic Barrett’s esophagus. Patients with DEVLB have widespread LGD, with many having areas of focal HGD or early cancer within this area. We believe these patients are best treated with extensive EMR of the visibly abnormal area.
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spelling pubmed-69042342019-12-11 Diffuse endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (with video) Tsoi, Edward H. Fehily, Sasha Williams, Richard Desmond, Paul Taylor, Andrew Endosc Int Open Background  Low grade dysplasia (LGD) in Barrett’s esophagus (BE) has generally been considered as undetectable endoscopically. Aim  To describe a phenotype which consists of diffuse, endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (DEVLB), with often subtle but visible endoscopic changes seen with high definition white light (HDWL) and narrow-band imaging (NBI). Method  A systematic search of a prospectively collected database for patients satisfying predefined criteria for DEVLB and a review of endoscopic and histological features of biopsies and endoscopic mucosal resection (EMR) specimens. Results  Out of a total of 419 patients referred to our expert center for assessment of dysplastic Barrett’s esophagus during the period January 2009 to March 2018, there were 7 patients (1.7 %) who satisfied the criteria defined for DEVLB, identified on their initial assessment endoscopy. All patients were treated by EMR of visible abnormal mucosa during their assessment endoscopy at our tertiary referral center. There was a total of 47 EMR specimens obtained, with a median of 6 (IQR 5–9) EMR resection pieces per patient, of which 36 (77 %) contained LGD, 8 (17 %) high grade dysplasia (HGD), 2 (4 %) non-dysplastic Barrett’s esophagus (NDBE), and 1 (2 %) contained early esophageal adenocarcinoma (EAC). Conclusion  DEVLB is a distinct phenotype seen in a small but significant proportion of individuals with dysplastic Barrett’s esophagus. Patients with DEVLB have widespread LGD, with many having areas of focal HGD or early cancer within this area. We believe these patients are best treated with extensive EMR of the visibly abnormal area. © Georg Thieme Verlag KG 2019-12 2019-12-10 /pmc/articles/PMC6904234/ /pubmed/31828211 http://dx.doi.org/10.1055/a-1031-9327 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Tsoi, Edward H.
Fehily, Sasha
Williams, Richard
Desmond, Paul
Taylor, Andrew
Diffuse endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (with video)
title Diffuse endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (with video)
title_full Diffuse endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (with video)
title_fullStr Diffuse endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (with video)
title_full_unstemmed Diffuse endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (with video)
title_short Diffuse endoscopically visible, predominantly low grade dysplasia in Barrett’s esophagus (with video)
title_sort diffuse endoscopically visible, predominantly low grade dysplasia in barrett’s esophagus (with video)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904234/
https://www.ncbi.nlm.nih.gov/pubmed/31828211
http://dx.doi.org/10.1055/a-1031-9327
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