斑点状内脉络膜病(PIC)样反应在伴有假性黄斑样外观(EMAP)的广泛性黄斑萎缩3期。

Andrea Trinco, Francesco Romano, Alessandro Invernizzi, Chiara Zaffalon, Francesca Bosello, Stefano Casati, Federico Zicarelli, Rossella D'Introno, Giovanni Staurenghi, Anna Paola Salvetti
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引用次数: 0

摘要

目的:描述一例伴有假性黄斑样外观(EMAP)的广泛性黄斑萎缩患者的罕见并发症,提示该疾病晚期出现免疫失调。方法:病例报告。多模式成像-包括真彩色眼底摄影,蓝色自身荧光,高分辨率光学相干断层扫描(高分辨率OCT),扫描源OCT血管造影和染料血管造影-用于评估视网膜改变。结果:一名53岁女性,患有3期EMAP,表现为中度高反射性视网膜下物质共定位,右眼布鲁氏膜(Bruch’s membrane, BrM)大面积破裂。多模态成像排除了黄斑新生血管,提示诊断为点状内脉络膜病(PIC)样反应。口服类固醇治疗导致视网膜下炎性病变完全消退。结论:本病例突出了EMAP的一种新型炎症并发症。我们的研究结果强调了免疫失调在晚期EMAP中的潜在作用,并强调了多模态成像在这些患者的管理和随访中的价值。
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Punctate Inner Choroidopathy (PIC)-like Reaction in Stage 3 Extensive Macular Atrophy with Pseudodrusen-like Appearance (EMAP).

Purpose: To describe a rare complication in a patient with extensive macular atrophy with pseudodrusen-like appearance (EMAP), suggesting immune dysregulation in advanced stages of the disease.

Methods: Case Report. Multimodal imaging -including true-color fundus photography, blue autofluorescence, high-resolution optical coherence tomography (Hi-Res OCT), swept-source OCT angiography, and dye-based angiography- was used to evaluate retinal alterations.

Results: A 53-year-old woman with stage 3 EMAP presented with moderately hyperreflective subretinal material co-localizing with a large rupture of the Bruch's membrane (BrM) in the right eye. Multimodal imaging ruled out macular neovascularization, suggesting a diagnosis of punctate inner choroidopathy (PIC)-like reaction. Treatment with oral steroids led to complete regression of the subretinal inflammatory lesion.

Conclusions: This case highlights a novel inflammatory complication in EMAP. Our findings emphasize a potential role of immune dysregulation in late-stage EMAP and underscore the value of multimodal imaging in the management and follow-up of these patients.

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来源期刊
Retinal Cases and Brief Reports
Retinal Cases and Brief Reports Medicine-Ophthalmology
CiteScore
2.10
自引率
0.00%
发文量
342
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