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Clinically Mild Encephalitis/Encephalopathy With a Reversible Splenial Lesion Accompanied by Epstein-Barr Virus Hemophagocytic Lymphohistiocytosis: A Case Report and Review of the Literature.
Yamaguchi, Hiroshi; Ishida, Toshiaki; Yokoi, Takehito; Tanaka, Tsukasa; Maruyama, Azusa; Nagase, Hiroaki; Hasegawa, Daiichiro; Imadome, Ken-Ichi; Takeda, Hiroki; Kosaka, Yoshiyuki; Uetani, Yoshiyuki.
Afiliação
  • Yamaguchi H; Departments of *Emergency and Critical Care Medicine †Hematology and Oncology ‡Neurology, Hyogo Prefectural Kobe Children's Hospital, Kobe §Division of Advanced Medicine for Virus Infections, National Research Institute for Child Health and Development, Tokyo, Japan.
J Pediatr Hematol Oncol ; 39(2): e92-e96, 2017 03.
Article em En | MEDLINE | ID: mdl-27879539
ABSTRACT
Central nervous system involvement in hemophagocytic lymphohistiocytosis (HLH) is associated with a poor outcome. For such patients, it is unknown whether more aggressive therapies, such as intrathecal methotrexate or hydrocortisone, are inevitably required. We present a very rare case of 3-year-old Japanese girl who developed mild encephalitis/encephalopathy with a reversible splenial lesion, accompanied by Epstein-Barr virus-associated HLH, and review previous similar reports. Our case and previous reports suggest that mild encephalitis/encephalopathy with a reversible splenial lesion accompanied by Epstein-Barr virus-associated HLH has a relatively good prognosis, even in the absence of intrathecal treatments.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Corpo Caloso / Infecções por Vírus Epstein-Barr / Encefalite / Linfo-Histiocitose Hemofagocítica Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Corpo Caloso / Infecções por Vírus Epstein-Barr / Encefalite / Linfo-Histiocitose Hemofagocítica Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article