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Progressive multifocal leukoencephalopathy in the absence of immunosuppression

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. Treatm...

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Detalles Bibliográficos
Autores principales: Zucker, Benjamin E., Stacpoole, Sybil R. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790842/
https://www.ncbi.nlm.nih.gov/pubmed/29139004
http://dx.doi.org/10.1007/s13365-017-0592-2
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author Zucker, Benjamin E.
Stacpoole, Sybil R. L.
author_facet Zucker, Benjamin E.
Stacpoole, Sybil R. L.
author_sort Zucker, Benjamin E.
collection PubMed
description 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.
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spelling pubmed-57908422018-02-05 Progressive multifocal leukoencephalopathy in the absence of immunosuppression Zucker, Benjamin E. Stacpoole, Sybil R. L. J Neurovirol Case Report 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. Springer International Publishing 2017-11-14 2018 /pmc/articles/PMC5790842/ /pubmed/29139004 http://dx.doi.org/10.1007/s13365-017-0592-2 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Zucker, Benjamin E.
Stacpoole, Sybil R. L.
Progressive multifocal leukoencephalopathy in the absence of immunosuppression
title Progressive multifocal leukoencephalopathy in the absence of immunosuppression
title_full Progressive multifocal leukoencephalopathy in the absence of immunosuppression
title_fullStr Progressive multifocal leukoencephalopathy in the absence of immunosuppression
title_full_unstemmed Progressive multifocal leukoencephalopathy in the absence of immunosuppression
title_short Progressive multifocal leukoencephalopathy in the absence of immunosuppression
title_sort progressive multifocal leukoencephalopathy in the absence of immunosuppression
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790842/
https://www.ncbi.nlm.nih.gov/pubmed/29139004
http://dx.doi.org/10.1007/s13365-017-0592-2
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