Abstract
AbstractBackgroundAnti‐N‐methyl‐d‐aspartate receptor (NMDAR) encephalitis is a severe form of limbic encephalitis. Some patients with anti‐NMDAR encephalitis do not respond to standard immunotherapy, resulting in poor outcomes.Case presentationWe report an 18‐year‐old female patient with anti‐NMDAR encephalitis, without a tumor, who showed a marked response to cyclophosphamide. She was admitted due to a 1‐month history of headache, psychiatric symptoms, and consciousness disturbance. Despite administering first‐line immunotherapy, including steroid pulse, intravenous immunoglobulin, and plasma exchange, she developed orofacial dyskinesia, central hypoventilation, and status epilepticus. Involuntary movements and seizure began to decrease only after the administration of cyclophosphamide (CPM), and she showed gradual improvement over the next 5 years. In addition, significant recovery from brain atrophy was observed on follow‐up MRI.ConclusionsCyclophosphamide should be considered for nonresponders to first‐line immunotherapy.
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