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亚急性硬化性全脑炎(SSPE)

[Subacute sclerosing panencephalitis (SSPE)].

作者信息

Nihei K

机构信息

Department of Neurology, National Children's Hospital.

出版信息

Nihon Rinsho. 1997 Apr;55(4):908-15.

PMID:9103893
Abstract

Subacute sclerosing panencephalitis (SSPE) is one of the most important slow virus infection caused by measles virus in human. It have passed over 20 years since measles virus was found in the brain of SSPE patients. However, definite etiological mechanism is still unknown. In Japan, number of SSPE patients are gradually decreasing, but over 5 patients are reported every year. Recently, the age of onset of SSPE became higher, incubation period from measles to SSPE onset became to be more prolonged, and serum measles antibody titers became lower than before. From typical clinical findings, serum and CSF measles antibody titers and periodic complex high voltage slow waves with suppression burst, SSPE is suggested. It is not so difficult to make diagnosis. As the differential diagnosis, epilepsy, brain tumor, metabolic diseases, or psychological disorders are mentioned. Treatment for SSPE is still undetermined. At present, it is thought that combined treatment of oral inosinpranobex (isoprinosine) and intratechal or intraventricular interferon (IFN) administration is the most effective.

摘要

亚急性硬化性全脑炎(SSPE)是人类由麻疹病毒引起的最重要的慢病毒感染之一。自SSPE患者大脑中发现麻疹病毒以来已过去20多年。然而,确切的病因机制仍不清楚。在日本,SSPE患者数量逐渐减少,但每年仍有超过5例报告。最近,SSPE的发病年龄升高,从麻疹到SSPE发病的潜伏期变得更长,血清麻疹抗体滴度比以前更低。根据典型的临床表现、血清和脑脊液麻疹抗体滴度以及周期性复合高电压慢波伴抑制暴发,可提示SSPE。做出诊断并不困难。作为鉴别诊断,提及了癫痫、脑肿瘤、代谢性疾病或心理障碍。SSPE的治疗仍未确定。目前,认为口服肌苷 pranobex(异丙肌苷)与鞘内或脑室内注射干扰素(IFN)联合治疗最为有效。

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