Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis Mimicking a Primary Psychiatric Disorder in an Adolescent.


Autoria(s): Lebon S.; Mayor-Dubois C.; Popea I.; Poloni C.; Selvadoray N.; Gumy A.; Roulet-Perez E.
Data(s)

2012

Resumo

Anti-N-methyl-d-aspartate (anti-NMDA) receptor encephalitis likely has a wider clinical spectrum than previously recognized. This article reports a previously healthy 16-year-old girl who was diagnosed with anti-NMDA receptor encephalitis 3 months after onset of severe depression with psychotic features. She had no neurological manifestations, and cerebral magnetic resonance imaging (MRI) was normal. Slow background on electroencephalogram and an oligoclonal band in the cerebrospinal fluid prompted the search for anti-NMDA receptor antibodies. She markedly improved over time but remained with mild neuropsychological sequelae after a trial of late immunotherapy. Only a high index of suspicion enables recognition of the milder forms of the disease masquerading as primary psychiatric disorders.

Identificador

https://serval.unil.ch/?id=serval:BIB_063CB4EB47A9

isbn:1708-8283 (Electronic)

pmid:22408145

doi:10.1177/0883073812438099

isiid:000311515900019

Idioma(s)

en

Fonte

Journal of Child Neurology, vol. 27, no. 12, pp. 1607-1610

Tipo

info:eu-repo/semantics/article

article