Movement Disorders (revue)

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Acute reversible parkinsonism in Epstein-Barr virus-related encephalitis lethargica-like illness.

Identifieur interne : 001507 ( Ncbi/Merge ); précédent : 001506; suivant : 001508

Acute reversible parkinsonism in Epstein-Barr virus-related encephalitis lethargica-like illness.

Auteurs : Petia S. Dimova [Bulgarie] ; Veneta Bojinova ; Dimitar Georgiev ; Ivan Milanov

Source :

RBID : pubmed:16250020

English descriptors

Abstract

A 10-year-old boy presented with fever, headache, vomiting, and hypersomnolence. An akinetic-rigid syndrome with tremor, dysphagia, dysphonia, and sialorrhea, as well as pyramidal signs, developed. Slightly elevated protein content was found in the cerebrospinal fluid and serological investigations were suggestive of a primary Epstein-Barr virus infection. Magnetic resonance imaging (MRI) showed massive bilateral hyperintense striatal and punctiform periventricular lesions. After 2-month treatment with steroids and antiparkinsonian drugs, all features resolved without sequelae. Control MRI demonstrated only minimal residual lesions in both putamina. Strongly resembling the encephalitis lethargica-like syndrome, this case is an unusual presentation of parainfectious acute disseminated encephalitis.

DOI: 10.1002/mds.20742
PubMed: 16250020

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Le document en format XML

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<div type="abstract" xml:lang="en">A 10-year-old boy presented with fever, headache, vomiting, and hypersomnolence. An akinetic-rigid syndrome with tremor, dysphagia, dysphonia, and sialorrhea, as well as pyramidal signs, developed. Slightly elevated protein content was found in the cerebrospinal fluid and serological investigations were suggestive of a primary Epstein-Barr virus infection. Magnetic resonance imaging (MRI) showed massive bilateral hyperintense striatal and punctiform periventricular lesions. After 2-month treatment with steroids and antiparkinsonian drugs, all features resolved without sequelae. Control MRI demonstrated only minimal residual lesions in both putamina. Strongly resembling the encephalitis lethargica-like syndrome, this case is an unusual presentation of parainfectious acute disseminated encephalitis.</div>
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