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Extensive myelitis associated with anti-NMDA receptor antibodies
Authors:Olivier?Outteryck  author-information"  >  author-information__contact u-icon-before"  >  mailto:olivier.outteryck@chru-lille.fr"   title="  olivier.outteryck@chru-lille.fr"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Guillaume?Baille,Jér?me?Hodel,Marianne?Giroux,Arnaud?Lacour,Jér?me?Honnorat,Hélène?Zéphir,Patrick?Vermersch
Affiliation:1.Department of Neurology, EA2686,Université Lille Nord de France,Lille,France;2.Department of Neuroradiology,Université Lille Nord de France,Lille,France;3.French Reference Centre for Paraneoplastic Neurological Syndrome,Hospices Civils de Lyon, H?pital Neurologique,Bron,France;4.Lyon Neuroscience Research Center INSERM U1028/CNRS UMR 5292,Lyon,France;5.Université de Lyon, Université Claude Bernard Lyon 1,Lyon,France
Abstract:

Background

Encephalitis with anti-N-methyl-D-aspartate receptor antibodies (anti-NMDAR-Ab) is a rapid-onset encephalitis including psychosis, seizures, various movement disorders and autonomic system disturbances.

Case presentation

We report a very unusual case of extensive myelitis associated with anti-NMDAR-Ab. MRI also revealed a hyperintense T2 lesion, non-suggestive of MS, which progressively extended, associated with periventricular gadolinium enhancement visualized on brain MRI. Ophthalmological evaluation showed subclinical right optic neuritis. The absence of anti-AQP4 antibody argued against neuromyelitis optica spectrum disorder. A slight psychomotor slowing prompted us to search for various causes of autoimmune encephalitis. Anti-NMDAR-Ab was found in cerebrospinal fluid.

Conclusion

In patients with extensive myelitis who are seronegative for anti-AQP4 antibodies, and after other classical causes have been excluded, the hypothesis of atypical anti-NMDAR-Ab encephalitis should also be considered.
Keywords:
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