首页> 外文期刊>European journal of ophthalmology >Spectral domain OCT and autofluorescence imaging of unilateral acute idiopathic maculopathy.
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Spectral domain OCT and autofluorescence imaging of unilateral acute idiopathic maculopathy.

机译:单侧急性特发性黄斑病变的光谱域OCT和自体荧光成像。

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To report imaging findings of unilateral acute idiopathic maculopathy (UAIM).In this observational case report, the Spectralis acquisition system (Heidelberg Engineering, Germany), which includes spectral domain optical coherence tomography (OCT), multiple autofluorescence (AF), fluorescein angiography (FA), and indocyanine green (ICG) angiography, was used for monitoring onset and evolution of UAIM.A well-defined, bullous macular lesion was evident on color pictures, infrared imaging (IR), and AF. Fluorescein angiography and ICG similarly showed early hypofluorescence of the lesion and, exclusively on FA, mild staining. Notably, the definition and limits of the detachment were clearly identifiable on late-phase ICG, and formed a hypocyanescent area. Spectral domain OCT disclosed severe retinal pigment epithelium (RPE) but not neurosensory detachment; the distinction between the photoreceptors inner/outer segment line was nonapparent for the entire length of the lesion. At 7-week follow-up, visual acuity improved to 20/20, with resolution of the exudative detachment. Autofluorescence and FA imaging indicated normalization, and only IR showed the boundaries of the lesion as still identifiable. Infrared imaging also showed a central granular feature, suggesting persistent choroid and pigment alteration. Indocyanine green angiography still evidenced the early hypofluorescent halo that became more evident in the late phases without any staining of the dye. Tomography depicted a reconstituted fovea, in which the outer limiting membrane and the inner/outer segment junction returned detectable.Comprehensive evaluation of UAIM by AF, FA, ICG, and spectral domain OCT disclosed involvement of RPE, the neuroretina, and the choroid in the pathogenesis of the disease. Despite functional recovery, choroidal rather than retinal alteration could persist.
机译:报告单侧急性特发性黄斑病变(UAIM)的影像学发现。 FA)和吲哚菁绿(ICG)血管造影用于监测UAIM的发生和发展,在彩色照片,红外成像(IR)和AF上明显可见黄斑病灶清晰。荧光素血管造影术和ICG相似地显示了病变的早期低荧光,并且仅在FA上出现轻度染色。值得注意的是,脱离的定义和界限在后期ICG上很明显,并且形成了一个下氰区域。光谱域OCT显示严重的视网膜色素上皮(RPE),但未出现神经感觉脱离;感光器内/外段线之间的区别对于病变的整个长度是不明显的。在7周的随访中,视力提高到20/20,并解决了渗出性脱离。自体荧光和FA成像显示正常,只有IR显示病灶的边界仍可识别。红外成像还显示出中央颗粒状特征,表明持续存在脉络膜和色素改变。吲哚菁绿色血管造影仍显示出早期的低荧光光晕,该光晕在后期没有任何染料的染色时变得更加明显。体层摄影术描绘了一个重建的中央凹,其中外侧限制膜和内/外节连接返回可检测。AF,FA,ICG和光谱域OCT对UAIM的综合评估显示RPE,神经视网膜和脉络膜参与该病的发病机理。尽管功能恢复,脉络膜而非视网膜的改变仍会持续。

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