Anesthetic experience of a patient with Ohtahara syndrome: A case report / 대한마취과학회지
Korean Journal of Anesthesiology
; : 124-127, 2011.
Artigo
em Inglês
| WPRIM (Pacífico Ocidental)
| ID: wpr-149646
Biblioteca responsável:
WPRO
ABSTRACT
Ohtahara syndrome (OS) is a rare epileptic encephalopathy that is characterized by an abnormal electroencephalogram (EEG) and intractable seizures in the neonatal and early infantile period. The patient of this reported case was delivered normally at 39 weeks of gestation without any complication. One week after birth, seizures that were refractory to anticonvulsants started with repetitive clustered tonic spasms. The child had no abnormal findings on the initial laboratory investigations. But he was diagnosed with OS according to the frequent tonic spasms, an abnormal EEG pattern of suppression-burst and magnetic resonance imaging of cortical dysplasia. He was planned to undergo an operation for brain lesion. This report describes our experience with the general anesthetic management when we performed craniotomy and right hemispherotomy for a patient with OS.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Convulsões
/
Espasmo
/
Encéfalo
/
Imageamento por Ressonância Magnética
/
Craniotomia
/
Parto
/
Eletroencefalografia
/
Malformações do Desenvolvimento Cortical
/
Anticonvulsivantes
Limite:
Criança
/
Humanos
/
Gravidez
Idioma:
Inglês
Revista:
Korean Journal of Anesthesiology
Ano de publicação:
2011
Tipo de documento:
Artigo