Cruzeiro Marcelo Maroco, Vale Thiago Cardoso, Pires Leopoldo Antônio, Franco Gláucio Mendes
Neurology Service, Department of Internal Medicine, University Hospital, Federal University of Juiz de Fora, Avenida Rio Branco 2370/802, Juiz de Fora, MG, Brazil.
Arq Neuropsiquiatr. 2007 Dec;65(4A):1030-3. doi: 10.1590/s0004-282x2007000600024.
Subacute sclerosing panencephalitis (SSPE) is a progressive inflammatory disorder of the central nervous system with both poor prognosis and high mortality. The disease has been related to a persistent and aberrant measles virus infection and no effective treatment has been available. We report a case of SSPE with atypical features including seizures at onset and a fulminant course in a 8 years-old boy who had been previously immunized against measles.
亚急性硬化性全脑炎（SSPE）是一种中枢神经系统的进行性炎症性疾病，预后差且死亡率高。该疾病与持续性及异常的麻疹病毒感染有关，目前尚无有效的治疗方法。我们报告一例具有非典型特征的SSPE病例，该病例为一名8岁男孩，起病时有癫痫发作且病程呈暴发性，该男孩此前已接种过麻疹疫苗。
