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筛板的高分辨率体内成像。

High resolution in vivo imaging of the lamina cribrosa.

作者信息

Park Sung C, Ritch Robert

机构信息

Einhorn Clinical Research Center, New York Eye and Ear Infirmary, New York, NY, USA.

出版信息

Saudi J Ophthalmol. 2011 Oct;25(4):363-72. doi: 10.1016/j.sjopt.2011.07.007. Epub 2011 May 8.

DOI:10.1016/j.sjopt.2011.07.007
PMID:23960950
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3729385/
Abstract

The lamina cribrosa (LC) is considered to be the principal site of retinal ganglion cell axon injury in glaucoma. Imaging technology has steadily improved in recent years, allowing greater resolution of fine details of laminar structure. Histological studies have elucidated the details of LC structure, both in normal and glaucomatous eyes, but such studies are limited by smaller sample size, greater difficulty of conducting prospective studies, and possibility of altered tissue architecture during histologic processing. We reviewed the literature describing the LC in primate and human eyes using in vivo imaging devices and provided a brief explanation of the imaging technology and main results of the articles. We also discuss the advantages and limitations of each imaging modality described, including optic disk photography, confocal scanning laser ophthalmoscopy (CSLO) and optical coherence tomography (OCT). These modalities provide en face and/or cross-sectional images of the LC in vivo. Enhanced depth imaging OCT has recently led to important advances in imaging deeper structures of the posterior segment, including the LC. Adaptive optics has been adopted in CSLO and OCT imaging to correct for ocular aberration and has improved resolution and contrast of the LC images. Post-image processing techniques to compensate for light attenuation and enhance contrast in OCT images enabled better visualization of the LC beneath the neuroretinal rim, vascular structures, and scleral rim. Long-wavelength probe OCT has shown good visualization of the LC with improved penetration when combined with swept-source OCT. Contrast agents for enhanced visualization of selective target structures in OCT have been developed. All these technologies hold great promise for improved in vivo imaging of the LC and require further investigation.

摘要

筛板(LC)被认为是青光眼视网膜神经节细胞轴突损伤的主要部位。近年来,成像技术不断进步,能够更清晰地分辨筛板层结构的细微细节。组织学研究已经阐明了正常和青光眼眼中LC结构的细节,但此类研究受到样本量较小、进行前瞻性研究难度较大以及组织学处理过程中组织结构改变可能性的限制。我们回顾了使用体内成像设备描述灵长类和人眼LC的文献,并简要解释了成像技术和文章的主要结果。我们还讨论了所描述的每种成像方式的优缺点,包括视盘摄影、共焦扫描激光眼科显微镜(CSLO)和光学相干断层扫描(OCT)。这些方式能够在体内提供LC的正面和/或横截面图像。增强深度成像OCT最近在对包括LC在内的眼后段深层结构成像方面取得了重要进展。CSLO和OCT成像中采用了自适应光学技术来校正眼像差,提高了LC图像的分辨率和对比度。用于补偿OCT图像中光衰减并增强对比度的图像后处理技术能够更好地显示神经视网膜边缘、血管结构和巩膜边缘下方的LC。长波长探头OCT与扫频源OCT结合使用时,显示出对LC的良好可视化效果,穿透性有所提高。已经开发出用于在OCT中增强选择性目标结构可视化的造影剂。所有这些技术在改善LC的体内成像方面都具有巨大潜力,需要进一步研究。

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