| Literature DB >> 32535682 |
Marco Vabanesi1,2, Serena Marita Lazzarin1,2, Giordano Cecchetti1,2, Raffaella Fazio1, Giovanna Franca Fanelli2, Maria Antonietta Volonté1, Angela Genchi1, Antonino Giordano1, Vittorio Martinelli1, Sergio Colombo3, Paolo Beccaria3, Milena Mucci3, Jacopo Peccatori4, Massimo Filippi5,6,7,8, Fabio Minicucci2.
Abstract
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a potentially fatal autoimmune disease, characterized by autoantibody-mediated neurotransmission impairment in multiple brain locations. The course of this condition often comprises altered mental status, autonomic dysfunctions, refractory seizures and hyperkinetic movement disorders. Available disease-modifying therapies include corticosteroids, i.v. immunoglobulins, plasma exchange, rituximab and cyclophosphamide. In a subgroup of patients not responding to B-cell depletion, bortezomib, a proteasome inhibitor, has shown promising evidence of efficacy. The time course of recovery from acute phase may be very slow (weeks/months), and only few data are available in literature about the concurrent management of encephalitis-associated movement disorders. We report a case of severe anti-NMDAR encephalitis in a 29-year-old woman, not responsive to first- and second-line treatments, with persistent involuntary motor manifestations. Starting three months after symptom onset, four cycles of bortezomib have been administered; subsequently we observed a progressive improvement of neurological status. Meanwhile, motor manifestations were controlled after the administration of tramadol, a non-competitive NMDA receptor antagonist.Entities:
Keywords: Anti-NMDAR encephalitis; Autoimmune encephalitis; Bortezomib; EEG; Movement disorders
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Year: 2020 PMID: 32535682 DOI: 10.1007/s00415-020-09988-w
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849