Division of Epidemiology and Clinical Applications, National Eye Institute, NIH, Bethesda, Maryland.
Retin Cases Brief Rep. 2021 May 1;15(3):207-210. doi: 10.1097/ICB.0000000000000826.
To provide long-term, natural history data of a case of a subclinical choroidal neovascular membrane (CNVM) in the setting of age-related macular degeneration.
Retrospective review of the 10-year clinical course of a patient including multimodal imaging.
A 75-year-old white female with macular degeneration presented with visual acuity of 20/25 in the right eye and 20/40 in the left eye. In the left eye, a retinal pigment epithelial detachment with associated subretinal and intraretinal fluid was found on spectral domain optical coherence tomography. Fluorescein angiography was consistent with a predominately classic CNVM, which was well-visualized on indocyanine green angiography. Treatment was initiated with bevacizumab for 10 months that reduced the amount of subretinal and intraretinal fluid, but progressive geographic atrophy developed over the subsequent 9 years reducing vision to 20/100. Interestingly, at initial presentation, a nonexudative fibrovascular pigment epithelial detachment was detected in the right (contralateral) eye. This was monitored with multimodal imaging twice yearly for 10 years without any signs of exudation, and vision remained 20/25. Optical coherence tomography angiography revealed a remarkably similar appearance of the subclinical CNVM compared with indocyanine green angiography 10 years prior, suggesting anatomical stability.
The advent of optical coherence tomography angiography has increased the detection of subclinical CNVMs. Recent evidence suggests that subclinical CNVMs have a high rate of progression to exudation over 1 year, which raises the question of whether early treatment is beneficial. This case provides 10-year follow-up with multimodal imaging (fluorescein angiography, indocyanine green angiography, optical coherence tomography, and optical coherence tomography angiography) of a subclinical CNVM, which remained stable and without exudation, suggesting that they may be closely observed.
提供一例年龄相关性黄斑变性患者亚临床脉络膜新生血管膜(CNVM)的长期自然病史数据。
回顾性分析一名患者的 10 年临床病程,包括多模态成像。
一名 75 岁白人女性,右眼视力为 20/25,左眼视力为 20/40。左眼发现视网膜色素上皮脱离伴伴发性视网膜下和视网膜内液,频域光相干断层扫描显示。荧光素血管造影与典型 CNVM 一致,吲哚菁绿血管造影显示病变清晰。给予贝伐单抗治疗 10 个月,减少了视网膜下和视网膜内液,但随后 9 年内进行性地图状萎缩导致视力下降至 20/100。有趣的是,在最初的表现中,右眼(对侧)检测到非渗出性纤维血管色素上皮脱离。通过多模态成像每年监测两次,持续 10 年,无渗出迹象,视力保持 20/25。光学相干断层扫描血管造影显示亚临床 CNVM 的表现与 10 年前吲哚菁绿血管造影非常相似,提示解剖结构稳定。
光学相干断层扫描血管造影的出现增加了亚临床 CNVM 的检出率。最近的证据表明,亚临床 CNVM 在 1 年内有很高的渗出进展率,这引发了早期治疗是否有益的问题。本病例提供了 10 年的多模态成像(荧光素血管造影、吲哚菁绿血管造影、光学相干断层扫描和光学相干断层扫描血管造影)随访,显示亚临床 CNVM 保持稳定且无渗出,表明可以密切观察。