A Case of Cyclosporine A: Induced Encephalopathy in a Child with Nephrotic Syndrome / 대한소아신경학회지
Journal of the Korean Child Neurology Society
; (4): 342-346, 2000.
Article
em Ko
| WPRIM
| ID: wpr-179735
Biblioteca responsável:
WPRO
ABSTRACT
Cyclosporine A is the most frequently used immunosuppressive agent for prevention of graft versus host disease (GVHD) and treatment of frequently relapsing nephrotic syndrome in childhood. Some adverse effects such as hepatic and renal toxicity, have been frequently encountered. But central nervous system toxicity caused by cyclosporine A is rare, and the incidence of encephalopathy among patients recieving cyclosporine A is unknown. Brain magnetic resonance imaging is an essential tool for diagnosis of cyclosporine A neurotoxicity. It typically demonstrates nonenhancing symmetric subcortical, and sometimes deep white matter changes resembling edema with posterior hemisphere predominance. We report a child with nephrotic syndrome who developed encephalopathy during cyclosporine A therapy. Based on this study, we emphasize that careful follow up of patient's neurological finding is very important to prevent serious life-threatening complications.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Encéfalo
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Imageamento por Ressonância Magnética
/
Sistema Nervoso Central
/
Incidência
/
Seguimentos
/
Ciclosporina
/
Diagnóstico
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Edema
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Doença Enxerto-Hospedeiro
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Síndrome Nefrótica
Tipo de estudo:
Diagnostic_studies
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Incidence_studies
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Observational_studies
/
Prognostic_studies
Limite:
Child
/
Humans
Idioma:
Ko
Revista:
Journal of the Korean Child Neurology Society
Ano de publicação:
2000
Tipo de documento:
Article