Anti-NMDA Encephalitis with Malignant Catatonia in an Adolescent: Differential Diagnosis and Response to Electroconvulsive Therapy
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Copyright (c) 2026 Revista de Psiquiatría Infanto-Juvenil

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https://doi.org/10.31766/revpsij.v43n1a4Keywords:
anti-NMDA encephalitis, malignant catatonia, differential diagnosis, psychosis, electroconvulsive therapyAbstract
Introduction: Anti-NMDA encephalitis is an autoimmune disease associated with the presence of anti-NMDA antibodies. Its clinical presentation and findings in complementary tests are nonspecific, which often delays diagnosis and treatment initiation. Malignant catatonia is a severe and potentially life-threatening mental state associated with autoimmune encephalitis. Case presentation: We present a case of anti-NMDA encephalitis in a 16-year-old female patient, who was admitted to a Child and Adolescent Psychiatry Unit after experiencing severe neurological and psychiatric symptoms. The condition was complicated by malignant catatonia and autonomic instability, with poor response to benzodiazepine treatment. The patient showed clinical improvement after the initiation of immunotherapy and electroconvulsive therapy. Conclusions: Electroconvulsive therapy is an effective treatment option for patients with this profile and should be considered for the treatment of anti-NMDA encephalitis with catatonia refractory to benzodiazepines.
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