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HYPERREFLECTIVE FOVEAL SPOTS 患者的玻璃体视网膜异常:定性和定量分析。

HYPERREFLECTIVE FOVEAL SPOTS IN PATIENTS WITH VITREORETINAL ANOMALIES: A Qualitative and Quantitative Analysis.

机构信息

Department of Ophthalmology, San Raffaele Scientific Institute, Vita-Salute University, Milan, Italy.

出版信息

Retina. 2020 Apr;40(4):705-709. doi: 10.1097/IAE.0000000000002505.

DOI:10.1097/IAE.0000000000002505
PMID:30845025
Abstract

PURPOSE

To describe structural optical coherence tomography (OCT) and OCT angiography features in patients who have developed hyperreflective foveal spots with or without vitreomacular interface abnormalities or with vitreous adhesion alone.

METHODS

The study design was observational and cross sectional. The presence of defined epiretinal membrane was considered an exclusion criterion. All patients underwent complete ophthalmologic examination, with structural OCT and OCT angiography acquisitions. Both qualitative and quantitative analyses of OCT angiography reconstructions were performed for superficial capillary plexus, deep capillary plexus, and choriocapillaris.

RESULTS

Thirty patients (20 men; mean age, 55.2 years) showing hyperreflective foveal spots on structural OCT and 30 healthy control subjects (20 men; mean age, 54.7 years) were enrolled. Best-corrected visual acuity was 0.0 ± 0.0 logarithm of the minimum angle of resolution (20/20 Snellen) for both patients and control subjects. Following global and parafoveal/extrafoveal analyses, both superficial capillary plexus and deep capillary plexus showed significant reduction (P < 0.001). Significant superficial capillary plexus and deep capillary plexus changes were also detected in contralateral eyes (P < 0.001).

CONCLUSION

Hyperreflective foveal spots might be seen as the initial effect of traction forces causing Müller cell and external retinal layer disruption, leading to the onset of vitreomacular disease. These changes also have an effect on the retinal vascular network. Further larger prospective studies are necessary to confirm our findings.

摘要

目的

描述出现伴或不伴玻璃体黄斑界面异常或仅伴玻璃体粘连的强反射性黄斑斑点的患者的结构光相干断层扫描(OCT)和 OCT 血管造影特征。

方法

研究设计为观察性和横断面研究。存在明确的视网膜前膜被认为是排除标准。所有患者均接受全面眼科检查,包括结构 OCT 和 OCT 血管造影采集。对浅层毛细血管丛、深层毛细血管丛和脉络膜毛细血管进行 OCT 血管造影重建的定性和定量分析。

结果

30 名(20 名男性;平均年龄 55.2 岁)出现结构 OCT 上强反射性黄斑斑点的患者和 30 名健康对照者(20 名男性;平均年龄 54.7 岁)被纳入研究。最佳矫正视力均为 0.0±0.0 对数最小角分辨率(20/20 Snellen)。进行全视网膜和旁中心/中心外分析后,浅层毛细血管丛和深层毛细血管丛均显示出显著减少(P<0.001)。对侧眼也检测到明显的浅层毛细血管丛和深层毛细血管丛变化(P<0.001)。

结论

强反射性黄斑斑点可能是牵引力量导致 Müller 细胞和外层视网膜层破裂的初始效应,导致玻璃体黄斑疾病的发生。这些变化也会对视网膜血管网络产生影响。需要进一步进行更大规模的前瞻性研究来证实我们的发现。

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