Tumor heterogeneity and carcinoma in resected specimens of gastric low-grade dysplasia: A retrospective single center study.

Lesions diagnosed as gastric low-grade dysplasia (LGD) may be pathologically upgraded to early gastric cancer (EGC) or high-grade dysplasia (HGD) after endoscopic resection (ER). In this study, we investigated the risk factors for pathological upgrades after ER and assessed the reason for these upgr...

Full description

Bibliographic Details
Main Authors: Ga-Yeong Shin, Jun Young Park, Sung Hak Lee, Yu Kyung Cho, Myung-Gyu Choi, Jae Myung Park
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0280735
_version_ 1828052283150041088
author Ga-Yeong Shin
Jun Young Park
Sung Hak Lee
Yu Kyung Cho
Myung-Gyu Choi
Jae Myung Park
author_facet Ga-Yeong Shin
Jun Young Park
Sung Hak Lee
Yu Kyung Cho
Myung-Gyu Choi
Jae Myung Park
author_sort Ga-Yeong Shin
collection DOAJ
description Lesions diagnosed as gastric low-grade dysplasia (LGD) may be pathologically upgraded to early gastric cancer (EGC) or high-grade dysplasia (HGD) after endoscopic resection (ER). In this study, we investigated the risk factors for pathological upgrades after ER and assessed the reason for these upgrades by retrospectively analyzing ER data between January 1999 and December 2019. We enrolled patients with LGD confirmed by forceps biopsy; the patients were classified into pathologically concordant (LGD) and upgraded (HGD and EGC) groups according to the pathology of their resected specimen. To determine the risk factors for upgrade, we compared the endoscopic findings of the concordant and upgraded groups via 1:1 matched case-control design. To find the reasons for discordance, all upgraded cases were pathologically re-evaluated. Among 1,643 cases of LGD, pathological upgrades were observed in 423 (25.7%) resected specimens and EGC was found in 111 (6.7%) lesions. After matching the upgraded and concordant cases, lesion sizes exceeding 1.5 cm (odds ratio (OR): 1.8; 95% CI: 1.1-3.0), mucosal nodularity (OR: 10.8; 95% CI: 5.6-21.0), heterogeneous color (OR: 3.0; 95% CI: 1.7-5.3), presence of erosion (OR: 2.7; 95% CI: 1.8-5.3), and open-type gastric atrophy (OR: 2.9; 95% CI: 1.7-4.9) were noted to be significantly associated with upgraded pathology to EGC. Among the EGC cases, 99 (89.2%) were found to have pre-existing dysplasia. In conclusion, endoscopic evaluations should be performed because of possible pathological upgrades and co-existence of carcinomas in LGDs, especially when they exhibit surface nodularity, erosion, heterogeneous color, and large size.
first_indexed 2024-04-10T19:51:13Z
format Article
id doaj.art-f6878f8c9218451b86eaafde8a8f22e7
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-10T19:51:13Z
publishDate 2023-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-f6878f8c9218451b86eaafde8a8f22e72023-01-28T05:31:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01181e028073510.1371/journal.pone.0280735Tumor heterogeneity and carcinoma in resected specimens of gastric low-grade dysplasia: A retrospective single center study.Ga-Yeong ShinJun Young ParkSung Hak LeeYu Kyung ChoMyung-Gyu ChoiJae Myung ParkLesions diagnosed as gastric low-grade dysplasia (LGD) may be pathologically upgraded to early gastric cancer (EGC) or high-grade dysplasia (HGD) after endoscopic resection (ER). In this study, we investigated the risk factors for pathological upgrades after ER and assessed the reason for these upgrades by retrospectively analyzing ER data between January 1999 and December 2019. We enrolled patients with LGD confirmed by forceps biopsy; the patients were classified into pathologically concordant (LGD) and upgraded (HGD and EGC) groups according to the pathology of their resected specimen. To determine the risk factors for upgrade, we compared the endoscopic findings of the concordant and upgraded groups via 1:1 matched case-control design. To find the reasons for discordance, all upgraded cases were pathologically re-evaluated. Among 1,643 cases of LGD, pathological upgrades were observed in 423 (25.7%) resected specimens and EGC was found in 111 (6.7%) lesions. After matching the upgraded and concordant cases, lesion sizes exceeding 1.5 cm (odds ratio (OR): 1.8; 95% CI: 1.1-3.0), mucosal nodularity (OR: 10.8; 95% CI: 5.6-21.0), heterogeneous color (OR: 3.0; 95% CI: 1.7-5.3), presence of erosion (OR: 2.7; 95% CI: 1.8-5.3), and open-type gastric atrophy (OR: 2.9; 95% CI: 1.7-4.9) were noted to be significantly associated with upgraded pathology to EGC. Among the EGC cases, 99 (89.2%) were found to have pre-existing dysplasia. In conclusion, endoscopic evaluations should be performed because of possible pathological upgrades and co-existence of carcinomas in LGDs, especially when they exhibit surface nodularity, erosion, heterogeneous color, and large size.https://doi.org/10.1371/journal.pone.0280735
spellingShingle Ga-Yeong Shin
Jun Young Park
Sung Hak Lee
Yu Kyung Cho
Myung-Gyu Choi
Jae Myung Park
Tumor heterogeneity and carcinoma in resected specimens of gastric low-grade dysplasia: A retrospective single center study.
PLoS ONE
title Tumor heterogeneity and carcinoma in resected specimens of gastric low-grade dysplasia: A retrospective single center study.
title_full Tumor heterogeneity and carcinoma in resected specimens of gastric low-grade dysplasia: A retrospective single center study.
title_fullStr Tumor heterogeneity and carcinoma in resected specimens of gastric low-grade dysplasia: A retrospective single center study.
title_full_unstemmed Tumor heterogeneity and carcinoma in resected specimens of gastric low-grade dysplasia: A retrospective single center study.
title_short Tumor heterogeneity and carcinoma in resected specimens of gastric low-grade dysplasia: A retrospective single center study.
title_sort tumor heterogeneity and carcinoma in resected specimens of gastric low grade dysplasia a retrospective single center study
url https://doi.org/10.1371/journal.pone.0280735
work_keys_str_mv AT gayeongshin tumorheterogeneityandcarcinomainresectedspecimensofgastriclowgradedysplasiaaretrospectivesinglecenterstudy
AT junyoungpark tumorheterogeneityandcarcinomainresectedspecimensofgastriclowgradedysplasiaaretrospectivesinglecenterstudy
AT sunghaklee tumorheterogeneityandcarcinomainresectedspecimensofgastriclowgradedysplasiaaretrospectivesinglecenterstudy
AT yukyungcho tumorheterogeneityandcarcinomainresectedspecimensofgastriclowgradedysplasiaaretrospectivesinglecenterstudy
AT myunggyuchoi tumorheterogeneityandcarcinomainresectedspecimensofgastriclowgradedysplasiaaretrospectivesinglecenterstudy
AT jaemyungpark tumorheterogeneityandcarcinomainresectedspecimensofgastriclowgradedysplasiaaretrospectivesinglecenterstudy