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Asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature

BACKGROUND: We report the development of asymptomatic progressive multifocal leukoencephalopathy in a patient with multiple sclerosis on natalizumab therapy. Progressive multifocal leukoencephalopathy often presents with debilitating neurologic symptoms. Very few cases have documented a completely a...

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Autores principales: Zhang, Yinan, Wright, Crystal, Flores, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026501/
https://www.ncbi.nlm.nih.gov/pubmed/29960601
http://dx.doi.org/10.1186/s13256-018-1727-7
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author Zhang, Yinan
Wright, Crystal
Flores, Angela
author_facet Zhang, Yinan
Wright, Crystal
Flores, Angela
author_sort Zhang, Yinan
collection PubMed
description BACKGROUND: We report the development of asymptomatic progressive multifocal leukoencephalopathy in a patient with multiple sclerosis on natalizumab therapy. Progressive multifocal leukoencephalopathy often presents with debilitating neurologic symptoms. Very few cases have documented a completely asymptomatic course of the disease. CASE PRESENTATION: A 26-year-old white woman with multiple sclerosis was treated with natalizumab. She was diagnosed as having progressive multifocal leukoencephalopathy based on characteristic magnetic resonance imaging lesions after 27 infusions of natalizumab. She had no neurologic deficits at the time of diagnosis and John Cunningham virus in cerebrospinal fluid was detected at 15 copies/ml. She was initially treated with mefloquine and mirtazapine and remained asymptomatic for 3 months. She later developed worsening magnetic resonance imaging lesions related to immune reconstitution inflammatory syndrome. At that time, she received intravenously administered immunoglobulin and high-dose intravenously administered methylprednisolone with radiologic improvement of the lesions. CONCLUSIONS: Our case report illustrates that early detection of asymptomatic progressive multifocal leukoencephalopathy and its subsequent treatment resulted in a benign clinical course. In consideration of the additional small number of cases of asymptomatic progressive multifocal leukoencephalopathy that have been reported, we conclude that routine magnetic resonance imaging surveillance is important for patients with multiple sclerosis who are at high risk for developing natalizumab-associated progressive multifocal leukoencephalopathy.
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spelling pubmed-60265012018-07-09 Asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature Zhang, Yinan Wright, Crystal Flores, Angela J Med Case Rep Case Report BACKGROUND: We report the development of asymptomatic progressive multifocal leukoencephalopathy in a patient with multiple sclerosis on natalizumab therapy. Progressive multifocal leukoencephalopathy often presents with debilitating neurologic symptoms. Very few cases have documented a completely asymptomatic course of the disease. CASE PRESENTATION: A 26-year-old white woman with multiple sclerosis was treated with natalizumab. She was diagnosed as having progressive multifocal leukoencephalopathy based on characteristic magnetic resonance imaging lesions after 27 infusions of natalizumab. She had no neurologic deficits at the time of diagnosis and John Cunningham virus in cerebrospinal fluid was detected at 15 copies/ml. She was initially treated with mefloquine and mirtazapine and remained asymptomatic for 3 months. She later developed worsening magnetic resonance imaging lesions related to immune reconstitution inflammatory syndrome. At that time, she received intravenously administered immunoglobulin and high-dose intravenously administered methylprednisolone with radiologic improvement of the lesions. CONCLUSIONS: Our case report illustrates that early detection of asymptomatic progressive multifocal leukoencephalopathy and its subsequent treatment resulted in a benign clinical course. In consideration of the additional small number of cases of asymptomatic progressive multifocal leukoencephalopathy that have been reported, we conclude that routine magnetic resonance imaging surveillance is important for patients with multiple sclerosis who are at high risk for developing natalizumab-associated progressive multifocal leukoencephalopathy. BioMed Central 2018-07-01 /pmc/articles/PMC6026501/ /pubmed/29960601 http://dx.doi.org/10.1186/s13256-018-1727-7 Text en © The Author(s). 2018 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Zhang, Yinan
Wright, Crystal
Flores, Angela
Asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature
title Asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature
title_full Asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature
title_fullStr Asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature
title_full_unstemmed Asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature
title_short Asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature
title_sort asymptomatic progressive multifocal leukoencephalopathy: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026501/
https://www.ncbi.nlm.nih.gov/pubmed/29960601
http://dx.doi.org/10.1186/s13256-018-1727-7
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