Encephalitis associated with Anti-n-methyl-d-aspartate receptor antibodies. Case report.
DOI:
https://doi.org/10.35305/fcm.v1i.33Keywords:
Antibodies, Anti—n—methyl—d—aspartate receptor, Autoinmmune encephalitis, N—methyl—d—aspartate receptors, Neuropsychiatric symptomsAbstract
Encephalitis associated with anti—N—methyl—D—aspartate (NMDA) receptor antibodies is an autoimmune neurological condition recently recognized in 2007. It mainly affects young adults—especially women—and children. A large percentage is associated with tumour processes. Patients develop neuropsychiatric symptoms in a rapid and sequential way and they have convulsive crises that rapidly result in decreasing levels of consciousness, mutism, catatonia and abnormal movements. It is a potentially reversible condition and the seriousness of its effects will depend on how soon the patient receives treatment. This paper describes the case of a young patient who initially displayed self—injurious behaviour and had hallucinations. Later, he had memory and language impairment, behavioral disorders, seizures and anti—NMDA receptor antibodies in the cerebrospinal fluid. He had a favourable response to immunoglobulins and corticosteroids with control and stabilization of the disease.
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