Department of Molecular Gastroenterology and Hepatology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Digestion. 2017;96(3):127-134. doi: 10.1159/000479553. Epub 2017 Aug 26.
BACKGROUND/AIMS: The diagnostic efficacy of magnifying blue laser imaging (M-BLI) and M-BLI in bright mode (M-BLI-bright) in the identification of early gastric cancer (EGC) was evaluated for comparison to that of magnifying narrow-band imaging (M-NBI).
This prospective, multicenter study evaluated 114 gastric lesions examined using M-BLI, M-BLI-bright, and M-NBI between May 2012 and November 2012; 104 EGCs were evaluated by each modality. The vessel plus surface classification system was used to evaluate the demarcation line (DL), microvascular pattern (MVP), and microsurface pattern (MSP).
M-BLI, M-BLI-bright, and M-NBI revealed a DL for 96.1, 98.1, and 98.1% and irregular MVP for 95.1, 95.1, and 96.2% of lesions, respectively, with no significant difference. Irregular MSP was observed by M-BLI, M-BLI-bright, and M-NBI in 97.1, 90.4, and 78.8% of lesions, respectively, with significant differences (p < 0.001). The proportion of moderately differentiated adenocarcinoma with irregular MSP on M-BLI and absent MSP on M-NBI was significantly higher than that with irregular MSP on M-BLI and M-NBI (35.0 and 9.9%, respectively; p = 0.002).
M-BLI and M-BLI-bright provided excellent visualization of microstructures and microvessels similar to M-NBI. Irregular MSP in a moderately differentiated adenocarcinoma might be frequently visualized using M-BLI and M-BLI-bright compared with using M-NBI.
背景/目的:本研究旨在比较放大蓝激光成像(M-BLI)和亮模式放大蓝激光成像(M-BLI-bright)与放大窄带成像(M-NBI)在诊断早期胃癌(EGC)中的诊断效能。
本前瞻性、多中心研究纳入了 2012 年 5 月至 2012 年 11 月期间使用 M-BLI、M-BLI-bright 和 M-NBI 检查的 114 个胃病变;每种方式均评估了 104 个 EGC。采用血管加表面分类系统评估边界线(DL)、微血管模式(MVP)和微表面模式(MSP)。
M-BLI、M-BLI-bright 和 M-NBI 分别显示 96.1%、98.1%和 98.1%的病变 DL 和不规则 MVP,差异无统计学意义。M-BLI、M-BLI-bright 和 M-NBI 分别观察到 97.1%、90.4%和 78.8%的病变不规则 MSP,差异有统计学意义(p < 0.001)。在 M-BLI 上有不规则 MSP 且 M-NBI 上无 MSP 的中分化腺癌比例显著高于在 M-BLI 和 M-NBI 上均有不规则 MSP 的中分化腺癌(35.0%和 9.9%;p = 0.002)。
M-BLI 和 M-BLI-bright 提供了与 M-NBI 相似的优异微观结构和微血管可视化效果。与 M-NBI 相比,在中分化腺癌中,不规则 MSP 可能更常通过 M-BLI 和 M-BLI-bright 观察到。