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Clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy

BACKGROUND AND STUDY AIMS: Although the Vienna Classification recommends endoscopic resection for gastric high-grade dysplasia (HGD), many resected lesions are diagnosed as gastric cancer after endoscopic resection. This study aims to evaluate the clinical outcomes of gastric HGD identified by endos...

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Autores principales: Ryu, Dae Gon, Choi, Cheol Woong, Kang, Dae Hwan, Kim, Hyung Wook, Park, Su Bum, Kim, Su Jin, Nam, Hyeong Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486495/
https://www.ncbi.nlm.nih.gov/pubmed/27822683
http://dx.doi.org/10.1007/s10120-016-0665-6
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author Ryu, Dae Gon
Choi, Cheol Woong
Kang, Dae Hwan
Kim, Hyung Wook
Park, Su Bum
Kim, Su Jin
Nam, Hyeong Seok
author_facet Ryu, Dae Gon
Choi, Cheol Woong
Kang, Dae Hwan
Kim, Hyung Wook
Park, Su Bum
Kim, Su Jin
Nam, Hyeong Seok
author_sort Ryu, Dae Gon
collection PubMed
description BACKGROUND AND STUDY AIMS: Although the Vienna Classification recommends endoscopic resection for gastric high-grade dysplasia (HGD), many resected lesions are diagnosed as gastric cancer after endoscopic resection. This study aims to evaluate the clinical outcomes of gastric HGD identified by endoscopic forceps biopsy (EFB) after endoscopic submucosal dissection (ESD) and factors associated with discrepant results. PATIENTS AND METHODS: From December 2008 to July 2015, a total of 427 lesions diagnosed as initial HGD by EFB were enrolled. The rate of early gastric cancer (EGC) and factors predicting diagnosis upgrade were analyzed retrospectively. RESULTS: Tumors ranged between 2 and 65 mm in size (median 12.59). En bloc and complete resection rates were 97.4 and 95.3%, respectively. The diagnostic discrepancy rate was 76.3%. Upgrade and downgrade rates of pathological diagnoses were 66.5 and 9.8%, respectively. Central depression (OR 4.151), nodular surface (OR 5.582), surface redness (OR 2.926), lesion location (upper third of the stomach) (OR 3.894), and tumor size ≥10 mm (OR 2.287) were significantly associated with EGC. Nodular surface (OR 2.746), submucosal fibrosis (OR 3.958), lesion location (upper third of the stomach) (OR 6.652), and tumor size ≥10 mm (OR 4.935) significantly predicted invasive submucosal cancer. CONCLUSIONS: Central depression, nodular surface, surface redness, lesion location, large tumor size, and submucosal fibrosis were associated with EGC or submucosal cancer. Caution must be used in treating lesions with these features with ESD.
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spelling pubmed-54864952017-07-17 Clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy Ryu, Dae Gon Choi, Cheol Woong Kang, Dae Hwan Kim, Hyung Wook Park, Su Bum Kim, Su Jin Nam, Hyeong Seok Gastric Cancer Original Article BACKGROUND AND STUDY AIMS: Although the Vienna Classification recommends endoscopic resection for gastric high-grade dysplasia (HGD), many resected lesions are diagnosed as gastric cancer after endoscopic resection. This study aims to evaluate the clinical outcomes of gastric HGD identified by endoscopic forceps biopsy (EFB) after endoscopic submucosal dissection (ESD) and factors associated with discrepant results. PATIENTS AND METHODS: From December 2008 to July 2015, a total of 427 lesions diagnosed as initial HGD by EFB were enrolled. The rate of early gastric cancer (EGC) and factors predicting diagnosis upgrade were analyzed retrospectively. RESULTS: Tumors ranged between 2 and 65 mm in size (median 12.59). En bloc and complete resection rates were 97.4 and 95.3%, respectively. The diagnostic discrepancy rate was 76.3%. Upgrade and downgrade rates of pathological diagnoses were 66.5 and 9.8%, respectively. Central depression (OR 4.151), nodular surface (OR 5.582), surface redness (OR 2.926), lesion location (upper third of the stomach) (OR 3.894), and tumor size ≥10 mm (OR 2.287) were significantly associated with EGC. Nodular surface (OR 2.746), submucosal fibrosis (OR 3.958), lesion location (upper third of the stomach) (OR 6.652), and tumor size ≥10 mm (OR 4.935) significantly predicted invasive submucosal cancer. CONCLUSIONS: Central depression, nodular surface, surface redness, lesion location, large tumor size, and submucosal fibrosis were associated with EGC or submucosal cancer. Caution must be used in treating lesions with these features with ESD. Springer Japan 2016-11-07 2017 /pmc/articles/PMC5486495/ /pubmed/27822683 http://dx.doi.org/10.1007/s10120-016-0665-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Ryu, Dae Gon
Choi, Cheol Woong
Kang, Dae Hwan
Kim, Hyung Wook
Park, Su Bum
Kim, Su Jin
Nam, Hyeong Seok
Clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy
title Clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy
title_full Clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy
title_fullStr Clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy
title_full_unstemmed Clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy
title_short Clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy
title_sort clinical outcomes of endoscopic submucosa dissection for high-grade dysplasia from endoscopic forceps biopsy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486495/
https://www.ncbi.nlm.nih.gov/pubmed/27822683
http://dx.doi.org/10.1007/s10120-016-0665-6
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