TY - JOUR
T1 - Encefalitis autoinmune mediada por anticuerpos contra el receptor n-metil-d-aspartato
T2 - Reporte de cuatro casos en Perú
AU - Palomino-Lescano, Henry
AU - Segura-Chávez, Darwin
AU - Quispe-Orozco, Darko
AU - Castro-Suarez, Sheila
AU - De la Cruz, Walter
AU - Zapata-Luyo, Willy
AU - Delgado-Ríos, José
AU - Cam, Juan
AU - Alvarado-Morales, Marcela
AU - Paredes-Carcasi, Lippmann
AU - Cornejo-Herrera, Iván
AU - Meza-Vega, María
N1 - Publisher Copyright:
© 2019, Instituto Nacional de Salud. All rights reserved.
PY - 2019/3
Y1 - 2019/3
N2 - 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.
AB - 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.
KW - Case reports
KW - N-methyl-d-aspartate antirreceptor encephalitis
KW - Peru
UR - http://www.scopus.com/inward/record.url?scp=85066479634&partnerID=8YFLogxK
U2 - 10.17843/rpmesp.2019.361.3936
DO - 10.17843/rpmesp.2019.361.3936
M3 - Artículo
C2 - 31116328
AN - SCOPUS:85066479634
SN - 1726-4634
VL - 36
SP - 138
EP - 144
JO - Revista Peruana de Medicina Experimental y Salud Publica
JF - Revista Peruana de Medicina Experimental y Salud Publica
IS - 1
ER -