Bilateral optic neuritis and encephalopathy as the atypical presentations of multiple sclerosis following severe acute respiratory syndrome coronavirus 2 infection

IF 1 Q4 OPHTHALMOLOGY Taiwan Journal of Ophthalmology Pub Date : 2024-01-05 DOI:10.4103/tjo.tjo-d-23-00124
Sheng-Yu Liu, Wan-Jen Hsieh, Hsueh-Wen Hsueh, Chao-Wen Lin
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Abstract

Numerous evidence suggests coronavirus disease 2019 (COVID-19) potentially triggers demyelinating diseases, inclusive of multiple sclerosis (MS), and acute disseminated encephalomyelitis (ADEM), and various mechanisms have been proposed. We report a 42-year-old male presented with bilateral optic neuritis and encephalopathy, 2 weeks following COVID-19 infection. He denied any history or family history of neurological and ocular diseases. Severe bilateral visual impairment (only light perception) and pain with eye movement were reported. Fundoscopy revealed bilateral optic disc swelling. Magnetic resonance imaging showed tortuous bilateral optic nerves with optic nerve and nerve sheath enhancement. Multiple hyperintense nodules in bilateral cerebral white matter were noted on fluid-attenuated inversion recovery T2-weighted imaging without diffusion restriction or gadolinium contrast enhancement. Hypointense nodules in cerebral white matter were also noted on T1-weighted imaging, which implied some old lesions. Dissemination in space and time and cerebrospinal fluid-specific oligoclonal bands confirmed the diagnosis of MS. Both serum aquaporin-4 and myelin oligodendrocyte glycoprotein antibodies were negative. He received pulse steroid therapy for 5 days, followed by slowly tapering oral prednisolone. His vision, ocular motion pain, and encephalopathy improved gradually. However, the visual outcome was still poor (bilateral 20/400), and optic atrophy was noticed during 1-year follow-up. To our knowledge, this is the first case of MS following severe acute respiratory syndrome coronavirus 2 infection presented with bilateral optic neuritis and encephalopathy. Since these manifestations are exceedingly rare in MS, we suspect acute immune reactions induced by COVID-19 could bring about the atypical ADEM-like presentations of MS.
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双侧视神经炎和脑病是严重急性呼吸系统综合征冠状病毒 2 感染后多发性硬化症的非典型表现
大量证据表明,2019 年冠状病毒病(COVID-19)可能引发脱髓鞘疾病,包括多发性硬化症(MS)和急性播散性脑脊髓炎(ADEM),并提出了各种机制。我们报告了一名 42 岁男性在感染 COVID-19 两周后出现双侧视神经炎和脑病的病例。他否认有任何神经系统和眼部疾病的病史或家族史。双侧视力严重受损(仅有光感),眼球活动时疼痛。眼底镜检查发现双侧视盘肿胀。磁共振成像显示双侧视神经迂曲,视神经和神经鞘强化。流体增强反转恢复T2加权成像显示,双侧大脑白质有多个高密度结节,但无弥散受限或钆对比剂增强。T1 加权成像还发现脑白质有低密度结节,这意味着一些陈旧性病变。空间和时间上的扩散以及脑脊液特异性寡克隆带证实了多发性硬化症的诊断。血清水波长蛋白-4和髓鞘少突胶质细胞糖蛋白抗体均为阴性。他接受了为期 5 天的脉冲类固醇治疗,随后缓慢减量口服泼尼松龙。他的视力、眼球运动疼痛和脑病逐渐好转。然而,视力仍然很差(双侧 20/400),随访 1 年期间发现视神经萎缩。据我们所知,这是第一例在感染严重急性呼吸综合征冠状病毒 2 后出现双侧视神经炎和脑病的多发性硬化症患者。由于这些表现在多发性硬化症中极为罕见,我们怀疑COVID-19诱导的急性免疫反应可能会导致多发性硬化症的非典型ADEM样表现。
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来源期刊
CiteScore
1.80
自引率
9.10%
发文量
68
审稿时长
19 weeks
期刊最新文献
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