Acute retinal pigment epitheliitis using adaptive optics imaging: a case report.

IF 1.7 4区 医学 Q3 OPHTHALMOLOGY BMC Ophthalmology Pub Date : 2024-11-25 DOI:10.1186/s12886-024-03768-0
P A T Heutinck, S Wooning, K Liman, M Durand, L Sanchez Brea, C C W Klaver, V J M Verhoeven, D Andrade De Jesus, A A H J Thiadens
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Abstract

Background: Acute Retinal Pigment Epitheliitis (ARPE, Krill's disease) is a rare inflammatory retinal disorder commonly affecting young adults. It often presents unilaterally with central vision disruption, and typically resolves with vision restoration within 6 to 12 weeks. The pathogenesis of ARPE remains a subject of ongoing debate. Adaptive Optics Flood Illumination Ophthalmoscopy (AO-FIO) imaging has emerged as a valuable tool capable of detecting early cone photoreceptor changes and recovery. This case study presents two patients with ARPE, with longitudinal follow-up using multimodal imaging, including optical coherence tomography (OCT) and AO-FIO.

Case presentations: A 30-year-old male presented with sudden vision loss in both eyes. The best corrected visual acuity (BCVA) was 20/33 and 20/40 Snellen in the right and left eye, respectively. OCT showed interruption of the ellipsoid zone (EZ) band and outer nuclear layer (ONL) in both eyes; AO-FIO imaging revealed a foveal lesion and diminished parafoveal cone density in both eyes compared to two age-matched controls. After 6 months, BCVA was restored to 20/20, and OCT showed recovery of the ONL and EZ. On AO-FIO, the foveal lesion was still present and the parafoveal cone density increased but remained reduced even up to 15 months after onset when compared to the controls. The second patient, a 30-year-old woman, presented with a unilateral drop in vision to 20/63 Snellen. OCT showed discontinuation of the EZ and hyperreflectivity within the ONL and retinal pigment epithelium in the affected eye. The unaffected eye showed no abnormalities. After 3 months, the BCVA improved to 20/16 Snellen and OCT showed recovery of the EZ. AO-FIO was conducted 9 months after onset and revealed reduced parafoveal cone density in the affected and non-affected eye compared to the controls while OCT still showed recovery of all retinal layers.

Conclusions: ARPE is a self-limiting disease with recovery of BCVA and OCT retinal layers within 6 months. However, our 2 cases showed that parafoveal cone density recovered during follow-up but did not reach levels observed in controls. AO-FIO is an imaging modality that enhances sensitivity in measurements and can therefore be used as a complementary tool for follow-up.

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利用自适应光学成像的急性视网膜色素上皮炎:病例报告。
背景:急性视网膜色素上皮炎(ARPE,克里尔氏病)是一种罕见的视网膜炎症性疾病,常见于青壮年。它通常表现为单侧中心视力障碍,一般在 6 至 12 周内视力恢复。ARPE 的发病机制仍是一个争论不休的话题。自适应光学泛光照明眼底镜(AO-FIO)成像已成为一种能够检测早期视锥光感受器变化和恢复的重要工具。本病例研究介绍了两名 ARPE 患者的情况,并使用光学相干断层扫描 (OCT) 和 AO-FIO 等多模态成像进行了纵向随访:一名 30 岁的男性患者突然双眼视力下降。右眼和左眼的最佳矫正视力(BCVA)分别为 20/33 和 20/40 Snellen。OCT显示双眼椭圆带(EZ)和核外层(ONL)中断;与两个年龄匹配的对照组相比,AO-FIO成像显示双眼均有眼窝病变,眼窝旁视锥密度降低。6 个月后,BCVA 恢复到 20/20,OCT 显示 ONL 和 EZ 恢复。在AO-FIO上,与对照组相比,眼窝病变仍然存在,眼底视锥密度增加,但直到发病后15个月仍有所降低。第二名患者是一名 30 岁的女性,单侧视力下降至 20/63 Snellen。OCT 显示,患眼的 EZ 消失,视网膜上皮和视网膜色素上皮内出现高反射。未受影响的眼睛未见异常。3 个月后,BCVA 改善到 20/16 Snellen,OCT 显示 EZ 恢复。发病9个月后进行了AO-FIO检查,结果显示,与对照组相比,患眼和未受影响眼的视锥旁密度降低,而OCT仍显示视网膜各层均已恢复:ARPE是一种自限性疾病,BCVA和OCT视网膜层可在6个月内恢复。结论:ARPE 是一种自限性疾病,BCVA 和 OCT 视网膜层会在 6 个月内恢复。AO-FIO 是一种成像模式,可提高测量的灵敏度,因此可用作随访的补充工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Ophthalmology
BMC Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
5.00%
发文量
441
审稿时长
6-12 weeks
期刊介绍: BMC Ophthalmology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of eye disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
期刊最新文献
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