Narumi Mari, Nishitsuka Koichi, Yamakawa Mitsunori, Yamashita Hidetoshi
Department of Ophthalmology and Visual Sciences, Yamagata University Faculty of Medicine, Yamagata, Japan.
Department of Diagnostic Pathology, Yamagata University Faculty of Medicine, Yamagata, Japan.
Acta Ophthalmol. 2015 Aug;93(5):e386-e390. doi: 10.1111/aos.12623. Epub 2015 Mar 9.
To confirm the efficacy of liquid-based cytology (LBC) method in the observation of vitreous cells in various vitreoretinal diseases in human.
Vitreous fluid samples from 30 eyes were obtained by 23-gauge 3-port pars plana vitrectomy. After making three ports, we collected vitreous specimen from the core vitreous cavity without infusion. We divided the samples into a quiescent group and an active group based on clinical signs of inflammation. To confirm availability of LBC preparation slides for immunostaining, we also performed immunocytochemistry (ICC) for CD68, RPE65 and DEC-205 (CD205) using LBC slides of 10 cell-rich cases including retinal detachment and endophthalmitis.
Using LBC method, small amounts of vitreous cells were observed efficiently. Vitreous cells were observed in inflammatory quiescent cases including macular pucker and macular hole. The number of vitreous cells increased significantly in the cases with clinically active inflammation (2297 versus 207 cells/ml, respectively, p < 0.01, Mann-Whitney U-test). The ICC results showed the presence of CD68(+) cells in all 10 cases. Large numbers of DEC-205(+) cells were observed in one case with infectious endophthalmitis. In the cases with retinal detachment, the predominant cell type was RPE65(+) . Neutrophils and lymphocytes were also observed.
The LBC method makes it possible to examine vitreous specimens easily and efficiently, facilitating the expedient diagnosis of vitreoretinal diseases, and the preparation slides are available for immunocytochemistry. This study also showed that vitreoretinal disease involves the migration of various types of cells including macrophages, neutrophils, lymphocytes, RPE65(+) pigmented cells and DEC-205(+) cells.
证实液基细胞学(LBC)方法在观察人类各种玻璃体视网膜疾病中玻璃体细胞方面的有效性。
通过23G三通道平坦部玻璃体切除术获取30只眼的玻璃体样本。制作三个通道后,在未灌注的情况下从玻璃体中央腔收集玻璃体标本。根据炎症的临床体征将样本分为静止组和活动组。为了证实LBC制备玻片用于免疫染色的可用性,我们还对包括视网膜脱离和眼内炎在内的10例细胞丰富病例的LBC玻片进行了CD68、RPE65和DEC-205(CD205)的免疫细胞化学(ICC)检测。
使用LBC方法能有效观察到少量玻璃体细胞。在包括黄斑皱襞和黄斑裂孔在内的炎症静止病例中观察到了玻璃体细胞。在临床炎症活动的病例中,玻璃体细胞数量显著增加(分别为2297个/毫升和207个/毫升,p<0.01,曼-惠特尼U检验)。ICC结果显示10例病例中均存在CD68(+)细胞。在1例感染性眼内炎病例中观察到大量DEC-205(+)细胞。在视网膜脱离病例中,主要细胞类型为RPE65(+)。还观察到了中性粒细胞和淋巴细胞。
LBC方法使玻璃体标本的检查变得轻松高效,有助于玻璃体视网膜疾病的快速诊断,且制备玻片可用于免疫细胞化学检测。本研究还表明,玻璃体视网膜疾病涉及多种类型细胞的迁移,包括巨噬细胞、中性粒细胞、淋巴细胞、RPE65(+)色素细胞和DEC-205(+)细胞。