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Encefalitis autoinmune mediada por anticuerpos contra el receptor N-metil-D-aspartato

Reporte de cuatro casos en Perú

Bibliographic Data

ID15534823
AuthorsHenry Palomino-Lescano (Instituto Nacional de Ciencias Neurológicas, corresponding author), Darwin Segura-Chávez (Instituto Nacional de Ciencias Neurológicas), Darko Quispe‐Orozco (0000-0003-3627-5439, Instituto Nacional de Ciencias Neurológicas), Darko Quispe-Orozco, Sheila Castro‐Suárez (0000-0003-0313-3987, Instituto Nacional de Ciencias Neurológicas), Sheila Castro-Suarez, Walter De la Cruz (Instituto Nacional de Ciencias Neurológicas), Willy Zapata-Luyo (Instituto Nacional de Ciencias Neurológicas), José Delgado-Ríos (Instituto Nacional de Ciencias Neurológicas), Juan Cam (Instituto Nacional de Ciencias Neurológicas), Marcela Alvarado-Morales (Instituto Nacional de Ciencias Neurológicas), Lippmann Paredes-Carcasi (Instituto Nacional de Ciencias Neurológicas), Iván Cornejo-Herrera (Hospital San Hipólito), María Meza-Vega (0000-0003-4166-6944, Instituto Nacional de Enfermedades Neoplásicas)
Year2019
Volume36
Issue1
Pages138-138
Publication date2019-03-20
Open AccessYes
TypeARTICLE
VenueRevista Peruana de Medicina Experimental y Salud Pública (JOURNAL)
Journal identifiersISSN: 1726-4634 • E-ISSN: 1726-4642
PublisherNational Institute of Health of Peru (PUBLISHER • PE)
DOI10.17843/rpmesp.2019.361.3936
PMID31116328
OpenAlexW2925060626
LanguageES
References cited1

Autoimmune encephalitis with antibodies against the N-methyl-D-aspartate receptor (anti-NMDAR) is a disorder mediated by antibodies against neural surface antigens, whose early diagnosis and timely treatment improve the prognosis of the disease. Four cases with the definitive diagnosis of autoimmune encephalitis by anti-NMDAR are presented, treated at the National Institute of Neurological Sciences in Lima-Peru. All patients had epileptic seizures and three cases developed a refractory epileptic state. In addition, three patients presented neuropsychiatric alterations, dyskinesias, and dysautonomia. Two cases required ventilatory support. All presented an abnormal electroencephalogram; two cases had pleocytosis in cerebrospinal fluid, and only one showed brain abnormalities on MRI. Regarding treatment, all patients received methylprednisolone immunotherapy and only two of them required plasma exchange for an ineffective response to corticosteroid treatment. After 12 months of hospital discharge, three patients were free of epileptic seizures and only one case did not achieve functional independence. These cases show that anti-NMDAR encephalitis is a treatable condition and its early recognition together with appropriate treatment (immunotherapy/plasmapheresis) are essential for a favorable evolution

Antibody · Autoantibody · Autoimmune encephalitis · Cerebrospinal fluid · Disease · Dysautonomia · Encephalitis · Epilepsy · Immune system · Immunotherapy · Limbic encephalitis · Methylprednisolone · Plasmapheresis · Pleocytosis · Psychiatry · Amino Acid Enzymes and Metabolism · Autoimmune Neurological Disorders and Treatments · Genetics and Neurodevelopmental Disorders · Medicine · Gastroenterology · Immunology · Internal Medicine · Pediatrics

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