Ji Xiao-Wei, Lin Jie, Wang Yan-Ting, Ruan Jing-Jing, Xu Jing-Hong, Song Kai, Mao Jian-Shan
Department of Gastroenterology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, Zhejiang Province, China.
Department of Pathology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, Zhejiang Province, China.
World J Gastrointest Oncol. 2024 Aug 15;16(8):3529-3538. doi: 10.4251/wjgo.v16.i8.3529.
Minute gastric cancers (MGCs) have a favorable prognosis, but they are too small to be detected by endoscopy, with a maximum diameter ≤ 5 mm.
To explore endoscopic detection and diagnostic strategies for MGCs.
This was a real-world observational study. The endoscopic and clinicopathological parameters of 191 MGCs between January 2015 and December 2022 were retrospectively analyzed. Endoscopic discoverable opportunity and typical neoplastic features were emphatically reviewed.
All MGCs in our study were of a single pathological type, 97.38% (186/191) of which were differentiated-type tumors. White light endoscopy (WLE) detected 84.29% (161/191) of MGCs, and the most common morphology of MGCs found by WLE was protruding. Narrow-band imaging (NBI) secondary observation detected 14.14% (27/191) of MGCs, and the most common morphology of MGCs found by NBI was flat. Another three MGCs were detected by indigo carmine third observation. If a well-demarcated border lesion exhibited a typical neoplastic color, such as yellowish-red or whitish under WLE and brownish under NBI, MGCs should be diagnosed. The proportion with high diagnostic confidence by magnifying endoscopy with NBI (ME-NBI) was significantly higher than the proportion with low diagnostic confidence and the only visible groups (94.19% > 56.92% > 32.50%, < 0.001).
WLE combined with NBI and indigo carmine are helpful for detection of MGCs. A clear demarcation line combined with a typical neoplastic color using nonmagnifying observation is sufficient for diagnosis of MGCs. ME-NBI improves the endoscopic diagnostic confidence of MGCs.
微小胃癌(MGCs)预后良好,但因其直径最大≤5mm,过小而难以通过内镜检测到。
探索微小胃癌的内镜检测及诊断策略。
这是一项真实世界观察性研究。回顾性分析了2015年1月至2022年12月期间191例微小胃癌的内镜及临床病理参数。重点回顾了内镜可发现机会及典型肿瘤特征。
本研究中所有微小胃癌均为单一病理类型,其中97.38%(186/191)为分化型肿瘤。白光内镜(WLE)检测出84.29%(161/191)的微小胃癌,白光内镜发现的微小胃癌最常见形态为隆起型。窄带成像(NBI)二次观察检测出14.14%(27/191)的微小胃癌,NBI发现的微小胃癌最常见形态为平坦型。另外3例微小胃癌通过靛胭脂三次观察检测出。若边界清晰的病变在白光内镜下呈现典型肿瘤颜色,如黄红色或白色,在NBI下呈褐色,则应诊断为微小胃癌。经窄带成像放大内镜(ME-NBI)诊断信心高的比例显著高于诊断信心低及仅可见病变组(94.19%>56.92%>32.50%,P<0.001)。
白光内镜联合NBI及靛胭脂有助于微小胃癌的检测。使用非放大观察时,清晰的分界线结合典型肿瘤颜色足以诊断微小胃癌。ME-NBI提高了微小胃癌的内镜诊断信心。