Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Gut Liver. 2011 Jun;5(2):187-93. doi: 10.5009/gnl.2011.5.2.187. Epub 2011 Jun 23.
BACKGROUND/AIMS: Gastric dysplasia is generally accepted to be the precursor lesion of gastric carcinoma. Approximately 25% to 35% of histological diagnoses based on endoscopic forcep biopsies for gastric dysplastic lesions change following endoscopic resection (ER). The aim of this study was to determine the predictive endoscopic features of high-grade gastric dysplasia (HGD) or early gastric cancer (EGC) following ER for lesions initially diagnosed as low-grade dysplasia (LGD) by a forceps biopsy.
To determine predictive variables for upgraded histology (LGD to HGD or EGC). The lesion size, gross endoscopic appearance, location, and surface nodularity or redness as well as the presence of a depressed portion, Helicobacter pylori infection, and intestinal metaplasia were retrospectively investigated.
Among 251 LGDs diagnosed by an initial forceps biopsy, the diagnoses of 100 lesions (39.8%) changed following the ER; 56 of 251 LGDs (22.3%) were diagnosed as HGD, 39 (15.5%) as adenocarcinoma, and 5 (2.0%) as chronic gastritis. In a univariate analysis, large lesions (>15 mm), those with a depressed portion, and those with surface nodularity were significantly correlated with a upgraded histology classification following ER. In a multivariate analysis, a large size (>15 mm; odds ratio [OR], 2.8; 95% confidence interval [CI], 1.46 to 5.43) and a depressed portion in the lesion (OR, 2.7; 95% CI, 1.44 to 5.03) were predictive factors for upgraded histology following ER.
Our study shows that a substantial proportion of diagnoses of low-grade gastric dysplasias based on forceps biopsies were not representative of the entire lesion. We recommend ER for lesions with a depressed portion and for those larger than 15 mm.
背景/目的:胃黏膜异型增生通常被认为是胃癌的癌前病变。大约 25%至 35%的胃黏膜异型增生内镜活检的组织学诊断在进行内镜下切除(ER)后发生改变。本研究旨在确定最初经内镜活检诊断为低级别异型增生(LGD)的患者,在 ER 后高级别胃黏膜异型增生(HGD)或早期胃癌(EGC)的预测性内镜特征。
为确定组织学升级(LGD 升级为 HGD 或 EGC)的预测变量,回顾性研究了病变大小、大体内镜表现、部位、表面结节或发红以及凹陷部分、幽门螺杆菌感染和肠上皮化生的存在情况。
在 251 例初始活检诊断为 LGD 的患者中,100 例(39.8%)的诊断在 ER 后发生改变;251 例 LGD 中,56 例(22.3%)诊断为 HGD,39 例(15.5%)诊断为腺癌,5 例(2.0%)诊断为慢性胃炎。单因素分析显示,大病变(>15mm)、凹陷部位和表面结节与 ER 后升级的组织学分类显著相关。多因素分析显示,病变大(>15mm;优势比[OR],2.8;95%置信区间[CI],1.46 至 5.43)和病变有凹陷部位(OR,2.7;95%CI,1.44 至 5.03)是 ER 后组织学升级的预测因素。
本研究表明,基于活检的胃黏膜低级别异型增生的诊断在很大程度上不能代表整个病变。我们建议对有凹陷部位和直径大于 15mm 的病变进行 ER。