Lee Jessica G, Spaide Richard F
Vitreoretinal Consultants of New York, Great Neck, New York.
Department of Ophthalmology, Northwell Health Eye Institute, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Great Neck, New York; and.
Retin Cases Brief Rep. 2024 Jan 1;18(1):87-90. doi: 10.1097/ICB.0000000000001313.
The purpose of this study was to describe findings derived from extensions of optical coherence tomography, including volume rendering and frame-averaged optical coherence tomography angiography (OCT-A), in a case of acute posterior multifocal placoid pigment epitheliopathy (APMPPE).
This is a case report of a patient with APMPPE imaged during the acute and convalescent stages.
A 20-year-old man presented with an acute change in vision. He had multiple yellow-white placoid lesions at the level of the retinal pigment epithelium in the macula and nasal to the optic nerve in both eyes. Within 2 weeks, his visual acuity worsened to 20/80 and 20/400 in the right and left eyes, respectively. Spectral domain OCT showed focal defects in the ellipsoid and retinal pigment epithelium layers. Volume-rendering OCT-A showed inflammatory cells in the outer nuclear layer above the APMPPE lesion. Frame-averaged OCT-A revealed significant loss of capillary flow signal within capillary segments of the choriocapillaris. Ten weeks after presentation, there was resolution of the placoid changes, discontinuance of the inflammatory infiltrate in the outer nuclear layer, and significant reconstitution of flow in the choriocapillaris. The visual acuity was 20/20 in both eyes.
Novel volume-rendered and frame-averaged OCT-A images in a patient with APMPPE allowed detection of inflammatory cell infiltrate in the outer nuclear layer and reversible capillary segment nonperfusion of associated APMPPE lesions. The findings suggest short-term insults to choriocapillaris function may be reversible and can be tracked with modern imaging techniques.
本研究旨在描述光学相干断层扫描扩展技术的研究结果,包括容积再现和帧平均光学相干断层扫描血管造影(OCT-A),应用于一例急性后极部多灶性扁平色素上皮病变(APMPPE)患者。
这是一份关于一名APMPPE患者在急性期和恢复期的病例报告。
一名20岁男性出现视力急性改变。双眼黄斑区及视神经鼻侧视网膜色素上皮层有多个黄白色扁平病变。2周内,其右眼和左眼视力分别恶化为20/80和20/400。光谱域光学相干断层扫描显示椭圆体层和视网膜色素上皮层有局灶性缺损。容积再现OCT-A显示APMPPE病变上方外核层有炎性细胞。帧平均OCT-A显示脉络膜毛细血管段内毛细血管血流信号显著丢失。就诊10周后,扁平病变消退,外核层炎性浸润停止,脉络膜毛细血管血流显著重建。双眼视力均为20/20。
APMPPE患者的新型容积再现和帧平均OCT-A图像能够检测出外核层的炎性细胞浸润以及相关APMPPE病变的可逆性毛细血管段无灌注。这些发现表明,脉络膜毛细血管功能的短期损伤可能是可逆的,并且可以用现代成像技术进行追踪。