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Autoimmune encephalitis associated with antibodies to leucine-rich glioma inactivated 1 (LGI1) is recently described and there is a lack of detailed reports on the treatment of relapsing or refractory cases and long-term outcomes. Two case reports are presented. Both cases had faciobrachial dystonic seizures (FBDS) and received rituximab after relapsing or refractory disease. Both cases achieved sustained clinical remission of up to 15 and 56 months respectively. Rituximab use allowed withdrawal of corticosteroids and was well tolerated. Randomized clinical trials are needed in LGI1 encephalitis and other autoimmune encephalitides.

More information Original publication

DOI

10.1016/j.jneuroim.2014.03.012

Type

Journal article

Publication Date

2014-06-15T00:00:00+00:00

Volume

271

Pages

66 - 68

Total pages

2

Keywords

Autoantibody, Cognition, Encephalitis, LGI1, Rituximab, VGKC, Adult, Aged, Antibodies, Antibodies, Monoclonal, Murine-Derived, Encephalitis, Female, Humans, Immunologic Factors, Intracellular Signaling Peptides and Proteins, Male, Proteins, Rituximab, Secondary Prevention, Seizures, Treatment Outcome