Kaise Mitsuru, Ohkura Yasuo, Iizuka Toshiro, Kimura Ryusuke, Nomura Kosuke, Kuribayashi Yasutaka, Yamada Akihiro, Yamashita Satoshi, Furuhata Tsukasa, Kikuchi Daisuke, Ogawa Osamu, Matsui Akira, Mitani Toshifumi, Hoteya Shu
Department of Gastroenterology, Toranomon Hospital, Tokyo, Japan.
Department of Pathology, Kyorin University School of Medicine, Tokyo, Japan.
Endoscopy. 2015 Jan;47(1):19-25. doi: 10.1055/s-0034-1377965. Epub 2014 Sep 15.
Endocytoscopy (ECS) enables in vivo microscopic imaging, which allows analysis of mucosal structures at the cellular level; however, limited data are available on the validity of ECS in the stomach. The aim of this study was to evaluate the feasibility of ECS in the diagnosis of early gastric cancer.
Gastric lesions that were the targets of histopathological diagnosis by endoscopic submucosal dissection or biopsy specimen were prospectively enrolled and evaluated using a single charge-coupled device-integrated endocytoscope, following double staining with crystal violet and methylene blue. High grade ECS atypia was defined according to specific irregularities in gland structure and cell nuclei. The primary end point was the accuracy of ECS diagnosis for gastric cancer, using histopathological diagnosis as the gold standard.
A total of 82 lesions were investigated, including 23 early gastric cancers, 10 gastric adenomas, and 49 non-neoplastic lesions. Ten lesions could not be clearly observed by ECS because of poor staining due to viscous mucus or plaque; thus, assessability rates with ECS were 88 % in total and 91 % for gastric cancer. High grade ECS atypia was observed in 86 % of assessable gastric cancers, but not in any cases of gastric adenomas or non-neoplastic lesions. The sensitivity, specificity, positive and negative predictive values of high grade ECS atypia as the criterion for the diagnosis of gastric cancer were 86 %, 100 %, 100 %, and 94 %, respectively. No serious complications occurred during or after the examinations.
ECS is a clinically feasible modality to obtain in vivo histology, with high diagnostic accuracy in gastric cancer.
内镜下细胞内镜检查(ECS)可进行体内微观成像,从而在细胞水平分析黏膜结构;然而,关于ECS在胃部的有效性的数据有限。本研究的目的是评估ECS在早期胃癌诊断中的可行性。
前瞻性纳入经内镜黏膜下剥离术或活检标本进行组织病理学诊断的胃部病变,并使用单电荷耦合器件集成式细胞内镜进行评估,先用结晶紫和亚甲蓝进行双重染色。根据腺体结构和细胞核的特定异常来定义高级别ECS异型性。以组织病理学诊断为金标准,主要终点是ECS对胃癌诊断的准确性。
共研究了82个病变,包括23例早期胃癌、10例胃腺瘤和49例非肿瘤性病变。由于黏液或斑块导致染色不佳,有10个病变无法通过ECS清晰观察到;因此,ECS的总体可评估率为88%,胃癌的可评估率为91%。在可评估的胃癌中,86%观察到高级别ECS异型性,但胃腺瘤或非肿瘤性病变均未观察到。以高级别ECS异型性作为胃癌诊断标准的敏感性、特异性、阳性预测值和阴性预测值分别为86%、100%、100%和94%。检查期间及检查后均未发生严重并发症。
ECS是一种临床上可行的获取体内组织学的方法,对胃癌具有较高的诊断准确性。