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急性后极部多灶性鳞状色素上皮病变的光学相干断层扫描血管造影

OCT Angiography in Acute Posterior Multifocal Placoid Pigment Epitheliopathy.

作者信息

Furino Claudio, Shalchi Zaid, Grassi Maria Oliva, Cardoso Joao N, Keane Pearse A, Niro Alfredo, Cicinelli Maria Vittoria, Reibaldi Michele, Boscia Francesco, Alessio Giovanni, Pavesio Carlos

出版信息

Ophthalmic Surg Lasers Imaging Retina. 2019 Jul 1;50(7):428-436. doi: 10.3928/23258160-20190703-04.

DOI:10.3928/23258160-20190703-04
PMID:31344242
Abstract

BACKGROUND AND OBJECTIVE

To describe retinal and choroidal findings in different stages of acute posterior multifocal placoid pigment epitheliopathy (APMPPE).

PATIENTS AND METHODS

Retrospective, noncomparative case series studied by fundus biomicroscopy, fundus autofluorescence (FAF), fluorescein angiography (FA), indocyanine green angiography (ICGA), spectral-domain optical coherence tomographic (SD-OCT), and swept-source OCT angiography (SS-OCTA).

RESULTS

Six eyes of three patients with bilateral APMPPE were included. FAF showed multifocal, branched patches of hyperautofluorescence with areas of hypoautofluorescence; FA disclosed early hypofluorescence, with late-phase hyperfluorescence; ICGA showed early and late-phase hypofluorescence. SD-OCT imaging revealed bilateral retinal thinning, external limiting membrane (ELM) disruption, and severe alteration of the photoreceptor-retinal pigment epithelium complex. SS-OCTA showed widespread multiple dark spots in the choriocapillaris in Cases 1 and 2. Rarefaction and voids in the vascular texture were also detected in the deep plexus, unlike in Case 3, where the lesions were smaller and earlier, suggesting that retina vasculature may be affected after the choriocapillaris obstruction.

CONCLUSIONS

APMPPE may result from a distinct focal ischemia in the choriocapillaris, and OCTA allowed the authors to localize exactly all the placoid lesions and monitor the areas of absent fluid signal. [Ophthalmic Surg Lasers Imaging Retina. 2019;50:428-436.].

摘要

背景与目的

描述急性后极部多灶性鳞状色素上皮病变(APMPPE)不同阶段的视网膜和脉络膜表现。

患者与方法

采用回顾性、非对照病例系列研究,通过眼底生物显微镜检查、眼底自发荧光(FAF)、荧光素血管造影(FA)、吲哚菁绿血管造影(ICGA)、光谱域光学相干断层扫描(SD - OCT)和扫频源光学相干断层血管造影(SS - OCTA)进行研究。

结果

纳入3例双侧APMPPE患者的6只眼。FAF显示多灶性、分支状的高自发荧光斑块,伴有低自发荧光区域;FA显示早期低荧光,晚期高荧光;ICGA显示早期和晚期低荧光。SD - OCT成像显示双侧视网膜变薄、外界膜(ELM)破坏以及光感受器 - 视网膜色素上皮复合体的严重改变。SS - OCTA显示病例1和病例2的脉络膜毛细血管中有广泛的多个暗点。在深层血管丛中也检测到血管纹理稀疏和空洞,与病例3不同,病例3的病变较小且出现较早,提示脉络膜毛细血管阻塞后视网膜血管可能受到影响。

结论

APMPPE可能由脉络膜毛细血管中独特的局灶性缺血引起,OCTA使作者能够准确地定位所有鳞状病变并监测无液体信号的区域。[《眼科手术、激光与视网膜成像》。2019;50:428 - 436。]

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