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未免疫抑制患者的进行性多灶性白质脑病。

Progressive multifocal leukoencephalopathy in the absence of immunosuppression.

机构信息

Imperial College School of Medicine, South Kensington Campus, London, SW7 2AZ, UK.

Jesus College, University of Cambridge, Cambridge, CB5 8BL, UK.

出版信息

J Neurovirol. 2018 Feb;24(1):119-122. doi: 10.1007/s13365-017-0592-2. Epub 2017 Nov 14.

Abstract

A 69-year-old woman presented with a cortical hand syndrome progressing over several weeks. MRI brain showed characteristic appearances of progressive multifocal leukoencephalopathy (PML), confirmed by detection of the JC virus in CSF, despite the absence of any evidence of immunosuppression. Treatment with mirtazapine, mefloquine and cidofovir did not affect the progression of the disease, which was fatal within 7 months of presentation. This report adds to the small case literature that suggests that PML can occur in immunocompetent people, albeit extremely rarely.

摘要

一位 69 岁女性因皮层手综合征在数周内逐渐加重而就诊。脑部 MRI 显示出进行性多灶性白质脑病(PML)的典型表现,尽管没有任何免疫抑制的证据,但通过检测脑脊液中的 JC 病毒得到了确认。米氮平、甲氟喹和更昔洛韦的治疗并未影响疾病的进展,患者在出现症状后的 7 个月内死亡。本报告增加了小病例文献,表明 PML 也可发生于免疫功能正常的人群中,尽管极其罕见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5596/5790842/7208c702c6f9/13365_2017_592_Fig1_HTML.jpg

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