| Literature DB >> 30293488 |
Vasilios C Constantinides1, Dimitrios S Kasselimis1,2, George P Paraskevas1, Maria Zacharopoulou1, Elisabeth Andreadou1, Maria-Eleftheria Evangelopoulos1, Elisabeth Kapaki1, Costas Kilidireas1, Eleftherios Stamboulis1, Constantin Potagas1.
Abstract
Anti-NMDA receptor (NMDA-r) encephalitis is a relatively rare cause of autoimmune encephalitis with divergent clinical presentations. We report a case of an adult patient with anti-NMDA-r encephalitis presenting with isolated, abrupt-onset aphasia. Her condition remained unaltered over a period of 6 months. The patients' electroencephalogram findings were typical for NMDA-r encephalitis; however, her magnetic resonance imaging and cerebrospinal fluid analysis were normal. She responded well to immunotherapy, and aphasia eventually resolved. The natural course of the present case contradicts the rapidly progressive nature of typical NMDA-r encephalitis. Furthermore, it broadens the clinical spectrum of anti-NMDA-r encephalitis, to incorporate isolated, nonprogressive aphasia.Entities:
Keywords: Anti-NMDA-r encephalitis; aphasia; cognitive decline; immunotherapy; language
Mesh:
Year: 2018 PMID: 30293488 DOI: 10.1080/13554794.2018.1524915
Source DB: PubMed Journal: Neurocase ISSN: 1355-4794 Impact factor: 0.881