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非典型亚急性硬化性全脑炎

Atypical subacute sclerosing panencephalitis.

作者信息

Nihei K, Kamoshita S, Mizutani H, Kitayama T, Nishimura H

出版信息

Acta Neuropathol. 1977 May 16;38(2):163-6. doi: 10.1007/BF00688565.

Abstract

An unusual case of panencephalitis in a 4-year-old Japanese boy, with onset at three months after measles infection and rapid progression to a comatose state in approximately one month, is described. A rapid rise in serum measles antibody titre after the onset of the symptoms, and the appearance of various abnormal antibodies in the serum, were noted. Pathologically, the brain showed sclerosing polio- and leucoencephalitis with diffuse gliosis and sporadic intranuclear inclusions. The process is suggested to be intermediate or transitional between acute measles encephalitis and SSPE.

摘要

本文描述了一名4岁日本男孩患全脑炎的罕见病例,该患儿在麻疹感染3个月后发病,约1个月内迅速发展为昏迷状态。症状出现后血清麻疹抗体滴度迅速上升,且血清中出现了各种异常抗体。病理检查显示,大脑呈现硬化性脊髓灰质炎和白质脑炎,伴有弥漫性胶质细胞增生和散在的核内包涵体。该病程被认为处于急性麻疹脑炎和亚急性硬化性全脑炎之间的中间或过渡阶段。

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