ACUTE POSTERIOR MULTIFOCAL PLACOID PIGMENT EPITHELIOPATHY AND PLACOID VARIANT DISEASES MASQUERADING AS AGE-RELATED MACULAR DEGENERATION IN THE ELDERLY: A Case Series.

IF 2.3 2区 医学 Q2 OPHTHALMOLOGY Retina-The Journal of Retinal and Vitreous Diseases Pub Date : 2024-10-01 DOI:10.1097/IAE.0000000000004191
John Yu Cheng, Ahmad Santina, J Ben Margines, Shilo Voichanski, Prithvi Ramtohul, Elodie Bousquet, Jacques Bijon, K Bailey Freund, Lawrence Yannuzzi, David Sarraf
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Abstract

Purpose: To report eight cases of acute posterior multifocal placoid pigment epitheliopathy (APMPPE) or persistent placoid maculopathy (PPM) initially masquerading as age-related macular degeneration in elderly individuals.

Methods: APMPPE or PPM eyes in patients above age 55 years with macular retinal pigment epithelium disruption including drusenoid lesions on macular examination and/or with multimodal imaging were included. At least one method of multimodal imaging including fluorescein angiography (FA), indocyanine green angiography, optical coherence tomography (OCT), and OCT angiography (OCTA) was performed in all eyes for diagnosis and to monitor for macular neovascularization.

Results: Eight elderly male patients presented with vision loss and were all initially diagnosed with non-neovascular or neovascular age-related macular degeneration. With the aid of multimodal retinal imaging, a final diagnosis of either APMPPE or PPM was rendered. With FA and indocyanine green angiography, choroidal hypoperfusion was detected in all but one eye. With OCT, the angular sign of Henle fiber layer hyperreflectivity was identified in >50% of eyes. With OCTA, inner choroidal flow deficits were detected in all eyes. Macular neovascularization requiring anti-vascular endothelial growth factor injection therapy complicated three of eight cases.

Conclusion: Both APMPPE and PPM may develop in elderly individuals and may masquerade as age-related macular degeneration on presentation. Multimodal imaging including FA, indocyanine green angiography, and OCTA are important diagnostic modalities to assess for inner choroidal hypoperfusion to arrive at an accurate diagnosis and to detect macular neovascularization, which frequently complicates APMPPE and PPM. In these patients, serial anti-vascular endothelial growth factor intravitreal injections are essential in treating macular neovascularization and in preventing significant vision loss.

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伪装成老年性黄斑变性的 APMPPE 和 Placoid 变异疾病:病例系列。
目的:报告八例老年人急性后多灶性胎盘状色素上皮病变(APMPPE)或持续性胎盘状黄斑病变(PPM)最初伪装成年龄相关性黄斑变性(AMD)的病例:方法:纳入55岁以上、黄斑检查和/或多模态成像显示黄斑RPE破坏(包括类虹膜病变)的APMPPE或PPM患者。对所有患者的眼睛进行至少一种多模式成像,包括荧光素血管造影(FA)、吲哚菁绿血管造影(ICGA)、光学相干断层扫描(OCT)和 OCT 血管造影(OCTA),以诊断和监测黄斑新生血管(MNV):结果:八名老年男性患者出现视力下降,最初均被诊断为非新生血管性或新生血管性黄斑变性。通过多模态视网膜成像,最终诊断为 APMPPE 或 PPM。通过 FA 和 ICGA,除一只眼睛外,其他所有眼睛都检测到脉络膜灌注不足。通过 OCT,在超过 50% 的眼球中发现了亨氏纤维层高反射角征(ASHH)。通过 OCTA,所有眼球均发现脉络膜内血流障碍。8个病例中有3个并发了需要注射抗血管内皮生长因子的MNV:结论:APMPPE 和 PPM 都可能发生在老年人身上,并且可能在发病时被伪装成 AMD。包括FA、ICGA和OCTA在内的多模态成像是评估内脉络膜灌注不足以得出准确诊断的重要诊断方法,也是检测MNV的重要诊断方法,MNV经常并发APMPPE和PPM。对于这些患者,连续的抗血管内皮生长因子(anti-VEGF)玻璃体内注射对于治疗 MNV 和防止视力严重下降至关重要。
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来源期刊
CiteScore
5.70
自引率
9.10%
发文量
554
审稿时长
3-6 weeks
期刊介绍: ​RETINA® focuses exclusively on the growing specialty of vitreoretinal disorders. The Journal provides current information on diagnostic and therapeutic techniques. Its highly specialized and informative, peer-reviewed articles are easily applicable to clinical practice. In addition to regular reports from clinical and basic science investigators, RETINA® publishes special features including periodic review articles on pertinent topics, special articles dealing with surgical and other therapeutic techniques, and abstract cards. Issues are abundantly illustrated in vivid full color. Published 12 times per year, RETINA® is truly a “must have” publication for anyone connected to this field.
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