| Literature DB >> 29258971 |
Katharina Hohenbichler1, Julie Lelotte2, Renaud Lhommel3, Riëm El Tahry1, Pascal Vrielynck4, Susana Ferrao Santos1.
Abstract
Rasmussen encephalitis is a rare, devastating condition, typically presenting in childhood. Cases of adult-onset Rasmussen have also been described, but the clinical picture is less defined, rendering final diagnosis difficult. We present a case of adult-onset Rasmussen encephalitis with dual pathology, associated with focal cortical dysplasia and encephalitis. We interpreted the Rasmussen encephalitis to be caused by severe and continuous epileptic activity due to focal cortical dysplasia. The best therapeutic approach for such cases remains unclear.Entities:
Keywords: adult-onset Rasmussen encephalitis; dual pathology; focal cortical dysplasia
Mesh:
Year: 2017 PMID: 29258971 DOI: 10.1684/epd.2017.0947
Source DB: PubMed Journal: Epileptic Disord ISSN: 1294-9361 Impact factor: 1.819