Spectrum and Evolution of Movement Disorder Phenomenology in a Pediatric Powassan Encephalitis Case Series.

IF 2.6 4区 医学 Q2 CLINICAL NEUROLOGY Movement Disorders Clinical Practice Pub Date : 2024-10-22 DOI:10.1002/mdc3.14245
Kathryn Yang, Rebecca Lindsay, Vicente Quiroz, Rasha Srouji, Darius Ebrahimi-Fakhari
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Abstract

Background: The Powassan virus is a rare neurotropic, tick-borne arbovirus associated with meningoencephalitis. Despite the virus's known predilection for the basal ganglia, there are no reports detailing the spectrum of movement disorders in children with Powassan meningoencephalitis.

Cases: We present 3 cases of pediatric Powassan encephalitis, highlighting the diverse and evolving movement disorders associated with this disease. We observed subcortical myoclonus and progressive generalized dystonia (patient 1), transient dyskinesias and refractory focal dystonia (patient 2), and generalized dystonia evolving into chorea and lingual dyskinesias (patient 3). One patient exhibited multifocal vasculitis on magnetic resonance imaging angiography, a novel finding.

Conclusions: Movement disorders were a primary source of the morbidity experienced by pediatric Powassan encephalitis patients throughout their disease course, underscoring the importance of regular monitoring and adaptable treatment strategies in this condition. Larger, prospective studies are necessary to fully delineate the spectrum of associated movement disorders in this rare and severe disease.

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小儿波瓦桑脑炎病例系列中运动障碍现象的频谱和演变。
背景:波瓦桑病毒是一种罕见的神经性蜱传虫媒病毒,与脑膜脑炎有关。尽管已知该病毒偏爱基底节,但目前还没有报告详细说明波瓦桑脑膜脑炎患儿运动障碍的范围:病例:我们介绍了3例小儿鲍瓦桑脑炎病例,突出强调了与该疾病相关的运动障碍的多样性和演变性。我们观察到皮层下肌阵挛和进行性全身肌张力障碍(患者 1)、一过性运动障碍和难治性局灶性肌张力障碍(患者 2),以及全身肌张力障碍演变为舞蹈症和舌运动障碍(患者 3)。一名患者的磁共振成像血管造影显示其患有多灶性血管炎,这是一项新发现:运动障碍是小儿波瓦桑脑炎患者在整个病程中发病的主要原因,这突出表明了定期监测和适应性治疗策略在这种疾病中的重要性。有必要进行更大规模的前瞻性研究,以全面界定这种罕见的严重疾病所导致的运动障碍。
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来源期刊
CiteScore
4.00
自引率
7.50%
发文量
218
期刊介绍: Movement Disorders Clinical Practice- is an online-only journal committed to publishing high quality peer reviewed articles related to clinical aspects of movement disorders which broadly include phenomenology (interesting case/case series/rarities), investigative (for e.g- genetics, imaging), translational (phenotype-genotype or other) and treatment aspects (clinical guidelines, diagnostic and treatment algorithms)
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