Severe coxsackie virus B5 encephalitis mimics autoimmune limbic encephalitis in a young woman under long-term B-cell depletion with ocrelizumab: A case report.

IF 5 2区 医学 Q1 CLINICAL NEUROLOGY
Jakob Stögbauer, Victoria Schegerer, Fabian K Berger, Walter Schulz-Schaeffer, Klaus Fassbender, Jasmin Naumann, Sigrun Smola, Janina Eisenbeis, Moritz Bewarder, Florian Rosar, Michael Kettner, Thomas Gilcher, Sabine Diedrich, Mathias Fousse
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引用次数: 0

Abstract

Background: B-cell-depleting therapies are increasingly being used to treat autoimmune diseases. Although thousands of patients are and have been treated with these agents, the data are not yet strong enough to identify rare side effects with certainty.

Methods: We report the case of a patient undergoing ocrelizumab therapy for relapsing multiple sclerosis who developed a severe limbic syndrome.

Results: Autoimmune pathogenesis was initially suspected, with worsening on immunosuppressive therapy. Later, after diagnosis of an enterovirus infection, treatment with ribavirin and favipiravir in combination with intravenous immunoglobulins was initiated. After 4 weeks of therapy, the patient's clinical condition had stabilized with residual cognitive deficits.

Conclusion: Diagnosis and treatment of enterovirus infections remain challenging, especially in patients receiving immunosuppressive therapy.

严重柯萨奇病毒B5脑炎模拟自身免疫性边缘脑炎在长期使用奥克雷单抗b细胞消耗的年轻女性:一个病例报告。
背景:b细胞消耗疗法越来越多地被用于治疗自身免疫性疾病。尽管成千上万的患者正在或已经接受了这些药物的治疗,但这些数据还不足以确定罕见的副作用。方法:我们报告了一例接受ocrelizumab治疗复发性多发性硬化症的患者,他发展为严重的边缘综合征。结果:最初怀疑自身免疫发病,免疫抑制治疗后病情加重。后来,在诊断出肠道病毒感染后,开始使用利巴韦林和法匹拉韦联合静脉注射免疫球蛋白进行治疗。经过4周的治疗,患者的临床状况趋于稳定,但仍存在认知缺陷。结论:肠病毒感染的诊断和治疗仍然具有挑战性,特别是在接受免疫抑制治疗的患者中。
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来源期刊
Multiple Sclerosis Journal
Multiple Sclerosis Journal 医学-临床神经学
CiteScore
10.90
自引率
6.90%
发文量
186
审稿时长
3-8 weeks
期刊介绍: Multiple Sclerosis Journal is a peer-reviewed international journal that focuses on all aspects of multiple sclerosis, neuromyelitis optica and other related autoimmune diseases of the central nervous system. The journal for your research in the following areas: * __Biologic basis:__ pathology, myelin biology, pathophysiology of the blood/brain barrier, axo-glial pathobiology, remyelination, virology and microbiome, immunology, proteomics * __Epidemology and genetics:__ genetics epigenetics, epidemiology * __Clinical and Neuroimaging:__ clinical neurology, biomarkers, neuroimaging and clinical outcome measures * __Therapeutics and rehabilitation:__ therapeutics, rehabilitation, psychology, neuroplasticity, neuroprotection, and systematic management Print ISSN: 1352-4585
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