Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3087215 | Pratique Neurologique - FMC | 2014 | 9 Pages |
Abstract
Acute inflammatory myelopathy, also named acute myelitis (AM), is a rare and etiologically heterogeneous syndrome. Diagnostic criteria are based on clinical, radiological and biological features that lead to classify myelitis into distinct subgroups: acute transverse myelitis, acute partial myelitis and longitudinally extensive acute transverse myelitis. Recent identification of aquaporin-4 antibodies have helped enable early identification of patients with neuromyelitis optica-associated myelitis. However, etiology remains unknown in a substantial portion of AM cases. Despite the absence of evidence, management of an acute episode of AM is currently based on high-dose intravenous methylprednisolone.
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Authors
R. Marignier,