Subacute Sclerosing Panencephalitis Causing Rapidly Progressive Dementia and Myoclonic Jerks in a Sexagenarian Woman

IF 2.5 Q2 CLINICAL NEUROLOGY Tremor and Other Hyperkinetic Movements Pub Date : 2019-08-27 DOI:10.7916/tohm.v0.680
A. J. Reyes, K. Ramcharan, Sean Perot, S. Giddings, F. Rampersad, R. Gobin
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引用次数: 4

Abstract

Background Subacute sclerosing panencephalitis (SSPE) is a disease of childhood and adolescence, but can affect adults. Rapidly progressive cognitive decline, seizures including myoclonic jerks, spasticity, ataxia, visual disturbances, and incontinence are typical manifestations. Case report A 62-year-old woman who presented with rapidly progressive dementia and myoclonus was diagnosed with SSPE. There was resolution of the movement disorder with clonazepam and valproic acid treatment and some amelioration of cognitive decline after 3 months of therapy with interferon alfa and isoprinosine. Discussion With the recent rise in measles cases worldwide, any increased incidence of SSPE would require vigilance for early interventions.
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一名性别歧视妇女的亚急性硬化性全脑炎导致快速进展性痴呆和肌阵挛性抽搐
背景亚急性硬化性全脑炎(SSPE)是一种儿童和青少年疾病,但可影响成人。快速进行性认知能力下降、癫痫发作(包括肌阵挛性抽搐、痉挛、共济失调、视觉障碍和失禁)是典型的表现。病例报告一位62岁的女性,表现为快速进行性痴呆和肌阵挛,被诊断为SSPE。氯硝西泮和丙戊酸治疗后运动障碍得到了缓解,干扰素α和异丙素治疗3个月后认知能力下降有所改善。讨论随着最近全球麻疹病例的增加,任何SSPE发病率的增加都需要警惕早期干预。
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来源期刊
CiteScore
4.00
自引率
4.50%
发文量
31
审稿时长
6 weeks
期刊最新文献
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