Remdesivir Treatment Outcomes of Subacute Sclerosing Panencephalitis Presenting with Macular Necrotizing Retinitis: A Case Report.

IF 2.6 4区 医学 Q2 OPHTHALMOLOGY
Aseel Gebara, Mohammed Homeidat, Tarek Keadan, Tamar Fisher-Negev, Esther Oiknine-Djian, Dana G Wolf, Hadas Mechoulam, Dana Ekstein, Radgonde Amer
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Abstract

Purpose: Subacute sclerosing panencephalitis (SSPE) is a fatally progressive neurodegenerative disorder caused by persistent measles virus infection of the CNS. We report on the visual and neurological outcomes of SSPE in a patient who presented with necrotizing retinitis three decades after measles infection.

Methods: Descriptive case report.

Results: A 31-year-old woman presented with sudden blurred vision of the right eye (RE). Visual acuity (VA) was finger counting in RE and 0.8 in the left eye (LE). Funduscopy revealed RE multifocal macular yellowish lesions, LE peripheral retinal atrophic scar and bilateral optic disc edema. OCT of RE showed "moth-eaten" macula. Elevated anti-measles IgG and positive oligoclonal bands were detected in the cerebrospinal fluid (CSF). Aqueous PCR was positive for Measles. Brain MRI showed mild hyperintense FLAIR signal in the parieto-occipital white matter. Electroencephalogram revealed mild generalized and left temporal focal slowing. Treatment with remdesivir was instituted in combination with intravenous immunoglobulins. Subsequently, intrathecal interferon-ɑ was administered. Macular necrosis progressed relentlessly. Remdesivir lowered measles IgG titer in CSF and serum and the titer re-increased once remdesivir was discontinued. The patient was well one-year later.

Conclusion: While remdesivir failed to arrest measles-associated macular necrosis, it may have prevented disease progression in the contralateral eye and in the CNS. To our knowledge, this is the first case of measles-associated necrotizing retinitis that was confirmed by a positive aqueous PCR. In the absence of an established treatment, vaccination remains the most effective modality. Further investigation of remdesivir as a potential treatment of SSPE is required.

瑞德西韦治疗以黄斑坏死性视网膜炎为表现的亚急性硬化性全脑炎的疗效:1例报告。
目的:亚急性硬化性全脑炎(SSPE)是一种由中枢神经系统持续麻疹病毒感染引起的致死性进行性神经退行性疾病。我们报告一例麻疹感染后30年出现坏死性视网膜炎的SSPE患者的视觉和神经预后。方法:描述性病例报告。结果:1例31岁女性,因右眼突发性视力模糊(RE)就诊。视敏度(VA)为指数,左眼为0.8。眼底镜示RE多灶黄斑淡黄色病变,LE周围视网膜萎缩性瘢痕及双侧视盘水肿。RE OCT示“虫蛀”黄斑。脑脊液中检测到抗麻疹IgG升高和阳性寡克隆条带。水溶液PCR检测麻疹阳性。脑MRI示顶枕白质轻度高FLAIR信号。脑电图显示轻度广泛性和左颞局灶性迟缓。瑞德西韦联合静脉注射免疫球蛋白治疗。随后给予鞘内干扰素。黄斑坏死持续发展。瑞德西韦降低脑脊液和血清中麻疹IgG的滴度,一旦停用瑞德西韦,滴度再次升高。一年后病人恢复健康。结论:虽然瑞德西韦未能阻止麻疹相关性黄斑坏死,但它可能阻止了对侧眼睛和中枢神经系统的疾病进展。据我们所知,这是第一例麻疹相关的坏死性视网膜炎,经阳性水性PCR证实。在缺乏既定治疗方法的情况下,疫苗接种仍然是最有效的方式。需要进一步研究瑞德西韦作为SSPE的潜在治疗方法。
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来源期刊
CiteScore
6.20
自引率
15.20%
发文量
285
审稿时长
6-12 weeks
期刊介绍: Ocular Immunology & Inflammation ranks 18 out of 59 in the Ophthalmology Category.Ocular Immunology and Inflammation is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished manuscripts directed to ophthalmologists and vision scientists. Published bimonthly, the journal provides an international medium for basic and clinical research reports on the ocular inflammatory response and its control by the immune system. The journal publishes original research papers, case reports, reviews, letters to the editor, meeting abstracts, and invited editorials.
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