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Mild encephalopathy with splenial lesion and parainfluenza virus infection

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Publisher DOI
10.1016/j.pediatrneurol.2012.11.007
PubMed ID
23419480
Description
Mild encephalopathy with reversible splenial lesions has mainly been associated with influenza A and B virus infection. Patients present with neurologic symptoms 1 to 3 days after a prodromal illness and recover completely within a few days. Magnetic resonance imaging typically shows reversible lesions with reduced diffusion in the corpus callosum, predominantly in the splenium. We report on a 5-year old Caucasian boy who was referred with recurrent seizures and decreased level of consciousness after a 2-day prodromal fever and cough. Magnetic resonance imaging showed cytotoxic edema of the entire corpus callosum and the adjacent periventricular white matter with diffusion restriction and faint T(2)-hyperintensity. Parainfluenza virus type 1-3 infection was documented by direct immunofluorescence in the initial nasopharyngeal swab, but polymerase chain reaction for parainfluenza virus type 1-4 in the cerebrospinal fluid remained negative. This is-to our knowledge-the first description of mild encephalopathy with reversible splenial lesions in association with parainfluenza virus infection. The pathogenesis of mild encephalopathy with reversible splenial lesions, however, still remains unclear, and further studies investigating detailed mechanisms that lead to the typical brain lesions are warranted.
Date of Publication
2013
Publication Type
Article
Language(s)
en
Contributor(s)
Abenhaim Halpern, Lea
Agyeman, Philipp Kwame Abayieorcid-logo
Universitätsklinik für Kinderheilkunde
Steinlin, Maja
Universitätsklinik für Kinderheilkunde
El-Koussy, Marwan
Universitätsinstitut für Diagnostische und Interventionelle Neuroradiologie
Grunt, Sebastian
Universitätsklinik für Kinderheilkunde
Additional Credits
Universitätsklinik für Kinderheilkunde
Universitätsinstitut für Diagnostische und Interventionelle Neuroradiologie
Series
Pediatric neurology
Publisher
Elsevier
ISSN
0887-8994
Access(Rights)
metadata.only
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