Hashimoto Hideaki, Kishi Shoji
Department of Ophthalmology, Gunma University School of Medicine, Maebashi, Gunma, Japan.
Department of Ophthalmology, Gunma University School of Medicine, Maebashi, Gunma, Japan.
Am J Ophthalmol. 2015 Apr;159(4):698-706. doi: 10.1016/j.ajo.2015.01.015. Epub 2015 Jan 26.
To observe the progression of affected lesions using ultra-wide-field fundus autofluorescence (FAF) in multiple evanescent white dot syndrome.
Retrospective, observational case series.
setting: Institutional.
14 eyes of 13 patients (mean age, 35.8 years) with acute disease unilaterally.
Patients underwent ultra-wide-field FAF, spectral-domain optical coherence tomography (SD OCT), multifocal electroretinography (mfERG), and Goldmann or automated perimetry; the best-corrected visual acuity (BCVA) and refractive error were measured.
Ability of ultra-wide-field FAF to detect lesions with greater sensitivity compared with color fundus photography.
Ultra-wide-field FAF imaging enabled improved visualization of the affected lesions and showed that the core lesion was in the posterior fundus involving the peripapillary retina and posterior pole and surrounded by hyper-autofluorescent spots outside the vascular arcade. The posterior lesions expanded rapidly and peripheral spots spread farther peripherally and reached a maximal extent during the acute stage. During follow-up, the peripheral hyper-autofluorescent spots resolved and then hyper-autofluorescence of the posterior fundus gradually faded. SD OCT showed diffuse disruption of the photoreceptor inner segment/outer segment junction (IS/OS) in the posterior fundus during the acute stage. The correlation between the IS/OS abnormality and hyper-autofluorescent areas was unclear. The disrupted IS/OS was restored with normalization of the FAF.
Ultra-wide-field FAF showed that the lesions arise from the peripapillary retina and the posterior pole and spread peripherally in a centrifugal manner during the acute stage. The hyper-autofluorescent spots faded from the periphery in a centripetal manner.
使用超广角眼底自发荧光(FAF)观察多灶性一过性白点综合征中受累病变的进展情况。
回顾性观察病例系列。
机构研究。
13例患者的14只眼(平均年龄35.8岁),均为单侧急性疾病。
患者接受超广角FAF、光谱域光学相干断层扫描(SD OCT)、多焦视网膜电图(mfERG)以及Goldmann或自动视野检查;测量最佳矫正视力(BCVA)和屈光不正。
与彩色眼底照相相比,超广角FAF检测病变的敏感性更高的能力。
超广角FAF成像能够更好地显示受累病变,表明核心病变位于眼底后部,累及视乳头周围视网膜和后极部,并被血管弓外的高自发荧光斑点所包围。后部病变迅速扩大,周边斑点向周边更远的区域扩散,并在急性期达到最大范围。随访期间,周边高自发荧光斑点消退,随后眼底后部的高自发荧光逐渐减弱。SD OCT显示急性期眼底后部光感受器内节/外节连接(IS/OS)弥漫性破坏。IS/OS异常与高自发荧光区域之间的相关性尚不清楚。随着FAF恢复正常,破坏的IS/OS也得以恢复。
超广角FAF显示病变起源于视乳头周围视网膜和后极部,并在急性期以离心方式向周边扩散。高自发荧光斑点以向心方式从周边消退。