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Cerebral posterior reversible encephalopathy syndrome in 9 children with hematological diseases / 中华神经医学杂志
Article em Zh | WPRIM | ID: wpr-1034738
Biblioteca responsável: WPRO
ABSTRACT
Objective To investigate the precipitating factors,clinical manifestations,magnetic resonance imaging (MRI) features and prognoses of children with posterior reversible encephalopathy syndrome (PRES) during the treatment of hematological diseases,and to improve the understanding of the diseases.Methods A total of 9 children with PRES,admitted to our hospital from January 2012 to December 2016,were chosen.The clinical data,including precipitating factors,clinical manifestations,MRI features and prognoses,were retrospectively analyzed.Results (1) Precipitating factors6 patients with acute lymphoblastic leukemia occurred PRES during remission induction therapy (6/9,66.7%) and 3 occurred PRES during oral cyclosporine A after hematopoietic stem cell transplantation or autoimmune diseases (3/9,33.3%).(2) Clinical manifestationsall of them were acute onset,and the main symptoms were seizures (8/9,88.9%) and hypertension (7/9,77.8%);some patients suffered from headache,vomiting,visual disturbances,disturbance of consciousness and poor mental symptoms.(3) Features of head MR imagingthe lesions were mainly located in the parietal-occipital lobe,showing patchy long T1 and long T2 signals,and bilateral imperfect symmetry;FLAIR imaging showed high signal distinctly,and other parts of brain could also been involved in.(4) Prognoses7 children (77.8%) recovered well,one (11.1%) left frequent seizures during 2 years of follow up,one (11.1%) left mental retardation.Conclusion Methotrexate,cyclosporine A and other agents are important incentives in children with PRES during the treatment of hematological diseases;seizures and hypertension are the main clinical manifestations;MR imaging is important in diagnosing the disease;and PRES is not completely reversible.
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Texto completo: 1 Índice: WPRIM Idioma: Zh Revista: Chinese Journal of Neuromedicine Ano de publicação: 2018 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Idioma: Zh Revista: Chinese Journal of Neuromedicine Ano de publicação: 2018 Tipo de documento: Article