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光学相干断层扫描特征与新生血管性年龄相关性黄斑变性的管理和非新生血管性年龄相关性黄斑变性的进展有关:临床病理相关性。

OPTICAL COHERENCE TOMOGRAPHY FEATURES RELEVANT TO NEOVASCULAR AGE-RELATED MACULAR DEGENERATION MANAGEMENT AND NONNEOVASCULAR AGE-RELATED MACULAR DEGENERATION PROGRESSION: CLINICOPATHOLOGIC CORRELATION.

机构信息

Department of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, Heersink School of Medicine, Birmingham, Alabama.

Department of Ophthalmology, University Hospital, Würzburg, Germany.

出版信息

Retin Cases Brief Rep. 2023 Jun 1;17(4S):S41-S46. doi: 10.1097/ICB.0000000000001356.

Abstract

PURPOSE

Clinicopathologic correlation of two optical coherence tomography (OCT) features in neovascular age-related macular degeneration.

METHODS

Case report, clinicopathologic correlation.

RESULTS

A patient in her 90s was diagnosed with Type 3 macular neovascularization secondary to age-related macular degeneration in the index right eye and underwent intravitreal antivascular endothelial growth factor treatment for 5 years. A double-layer sign on in vivo OCT was correlated to calcified drusen on histology. Furthermore, hyperfluorescence on fluorescein angiography corresponded on histology to choroidal hypertransmission on OCT and retinal pigment epithelium atrophy above calcified drusen.

CONCLUSION

A double-layer sign on OCT can represent nonneovascular subretinal pigment epithelium material including wide and flat calcific nodules. Furthermore, hyperfluorescence on FA, among different origins, can be due to a window defect corresponding to retinal pigment epithelium atrophy, which can be confirmed with OCT. Clinicopathological correlation using high-resolution histology can demonstrate the fine details available to clinical decision making through currently available in vivo OCT imaging.

摘要

目的

新生血管性年龄相关性黄斑变性两种光学相干断层扫描(OCT)特征的临床病理相关性。

方法

病例报告,临床病理相关性。

结果

一位 90 多岁的患者被诊断为右眼年龄相关性黄斑变性继发 3 型黄斑新生血管,并接受了 5 年的玻璃体腔内抗血管内皮生长因子治疗。活体 OCT 上的双层征与组织学上的钙化玻璃膜疣相关。此外,荧光素血管造影上的强荧光在组织学上与 OCT 上的脉络膜高透过和钙化玻璃膜疣上方的视网膜色素上皮萎缩相对应。

结论

OCT 上的双层征可代表包括宽而平的钙化结节在内的非新生血管性视网膜色素上皮下物质。此外,不同来源的 FA 上的强荧光可能是由于对应于视网膜色素上皮萎缩的窗缺陷,这可以通过 OCT 来证实。利用高分辨率组织学进行临床病理相关性研究,可以通过目前可用的活体 OCT 成像来展示临床决策所需的精细细节。

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