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一名4岁儿童,有异食癖、进行性共济失调和反应性降低。

A 4-year-old with pica, progressive incoordination, and decreased responsiveness.

作者信息

Dlugos D J, Brooks-Kayal A R

机构信息

Children's Hospital of Philadelphia, PA 19104, USA.

出版信息

Semin Pediatr Neurol. 1999 Sep;6(3):164-7. doi: 10.1016/s1071-9091(99)80007-2.

DOI:10.1016/s1071-9091(99)80007-2
PMID:10522333
Abstract

This article reports a typical case of subacute sclerosing panencephalitis (SSPE). The patient contracted measles as an infant during the 1989 to 1991 United States measles epidemic. At 4 1/2 years of age, he developed behavioral changes and quickly progressed through the typical clinical stages of SSPE. His EEG was characteristic. Serum and CSF measles immunoglobulin G were markedly elevated. He remains alive but is vegetative. To our knowledge, this is the first case of SSPE stemming from the 1989 to 1991 measles epidemic. Because infants--the group at highest risk to develop SSPE--were most severely affected by this measles outbreak, other cases of SSPE stemming from this epidemic may occur.

摘要

本文报告了一例亚急性硬化性全脑炎(SSPE)的典型病例。该患者在1989年至1991年美国麻疹流行期间还是婴儿时感染了麻疹。4岁半时,他出现行为改变,并迅速经历了SSPE的典型临床阶段。他的脑电图具有特征性。血清和脑脊液中的麻疹免疫球蛋白G显著升高。他仍然活着,但呈植物人状态。据我们所知,这是首例源于1989年至1991年麻疹流行的SSPE病例。由于婴儿——发生SSPE风险最高的群体——在这次麻疹疫情中受影响最为严重,可能还会出现源于这次疫情的其他SSPE病例。

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