非接触体内共聚焦激光扫描显微镜研究脱落综合征。

Zaher Sbeity, Pat-Michael Palmiero, Celso Tello, Jeffrey M Liebmann, Robert Ritch
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摘要

目的:利用非接触式体内激光扫描共聚焦显微镜观察脱落综合征(XFS)患者角膜、虹膜和晶状体的结构改变,并将其与临床特征联系起来。方法:对30只XFS患者的角膜、虹膜和晶状体进行成像,采用海德堡视网膜断层成像仪Rostock角膜模组(50倍非接触式尼康镜头,估计1 ~ 2微米横向分辨率,500 × 500微米视野)。连续的横切面图像和前段图像被拍摄和分析。结果:19只眼(63%)角膜间质和内皮可见不同数量和大小的散在性小的高反射性沉积物。虹膜前外表面和/或瞳孔边缘显示高反射沉积物,对应于脱落物质(XFM)和/或色素颗粒。前晶状体囊可见不同程度的瞳孔周围纤维性高反射沉积,高反射区中央可见上皮细胞,中间清晰区可见均匀上皮细胞。在4只假性晶状眼的前囊上,XFM表现为高反射的圆形沉积物。6眼(20%)后房瞳孔区房水中可见高反射性浮性沉积物。结论:非接触体内共聚焦显微镜可以在角膜、虹膜和晶状体中显示XFM。这项新技术可以通过提供亚临床细胞病理信息,如早期颗粒前XFS,提高对前节异常的早期检测。
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Noncontact in vivo confocal laser scanning microscopy of exfoliation syndrome.

Purpose: To visualize structural alterations of the cornea, iris, and lens in patients with exfoliation syndrome (XFS) using a noncontact in vivo laser scanning confocal microscope and to correlate these with the clinical features.

Methods: The cornea, iris, and lens of 30 eyes with XFS were imaged using the Rostock Cornea Module of Heidelberg Retina Tomograph II (50x noncontact Nikon lens, an estimated 1 to 2 mum transverse resolution, 500x500-mum field of view). Serial transverse section images, as well as anterior segment photographs, were taken and analyzed.

Results: The corneal stroma and endothelium of 19 eyes (63%) showed different amounts and sizes of scattered small hyperreflective deposits. The irides revealed hyperreflective deposits on the anterior outer surfaces and/or pupillary margin corresponding to exfoliation material (XFM) and/or pigment granules. The anterior lens capsule showed varying degrees of peripupillary fibrillar hyperreflective deposits, hyperreflective areas with apparent epithelial cells centrally, and uniform epithelial cells in the clear intermediate zone. On the anterior capsule in 4 pseudophakic eyes, XFM appeared as hyperreflective round deposits. Hyperreflective floating deposits were seen in the aqueous humor in the pupillary region of the posterior chamber of 6 eyes (20%).

Conclusions: Noncontact in vivo confocal microscopy permits visualization of XFM in the cornea, iris, and lens. This new technique may improve early detection of anterior segment abnormalities by providing information about subclinical cellular pathology, such as early pregranular XFS.

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