63岁女性的亚急性硬化性全脑炎,表现为全身性舞蹈病。

IF 0.9 Q4 CLINICAL NEUROLOGY
Neurohospitalist Pub Date : 2023-10-01 Epub Date: 2023-05-19 DOI:10.1177/19418744231177105
Ritwick Mondal, Shramana Deb, Manoj Mahata, Somesh Saha, Durjoy Lahiri, Julián Benito-León
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引用次数: 0

摘要

麻疹病毒在儿童和青少年早期的持续感染很少会导致一种致命的进行性神经退行性疾病,称为亚急性硬化性全脑炎(SSPE),其特征是行为障碍和智力残疾,随后是肌阵挛抽搐和偶尔的负性肌阵痛。运动障碍很少出现在SSPE中。我们在此报告一位63岁的女性,全身性舞蹈病是第一阶段SSPE的主要表现。就患者的年龄和临床表现而言,我们的病例是非典型的,伴有全身性舞蹈病和双侧壳核和尾状核信号高信号。虽然非常罕见,但神经学家应该将SSPE作为运动障碍患者的鉴别诊断。麻疹流行国家应更加警惕SSPE的非典型和罕见表现,如全身性舞蹈病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subacute Sclerosing Panencephalitis in a 63-Year-Old Woman Presenting as Generalized Choreoathetosis.

The persistence of measles virus infection in childhood and early adolescence can rarely lead to a fatal progressive neurodegenerative disorder known as subacute sclerosing panencephalitis (SSPE), characterized by behavioral disturbances and intellectual disability followed by myoclonic jerks and occasional negative myoclonus. Movement disorders are rarely presenting manifestations in SSPE. We herein report a 63-year-old woman with generalized choreoathetosis as the presenting manifestation of stage-I SSPE. Our case was atypical for the patient's age and clinical presentation with generalized choreoathetosis and bilateral putaminal and caudate nucleus signal hyperintensity. Though highly uncommon, neurologists should keep SSPE as a differential diagnosis among patients with movement disorders. Measles-endemic countries should be more vigilant to the atypical and rare presentations of SSPE, such as generalized choreoathetosis.

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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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