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Diagnostic delay in progressive multifocal leukoencephalopathy

We investigated delay in diagnosing progressive multifocal leukoencephalopathy (PML). The median time from initial symptom to diagnosis was 74 days (range 1–1643) in 111 PML patients seen at our institution from 1993 to 2015. Another diagnosis was considered before PML in nearly two–thirds, and more...

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Autores principales: Miskin, Dhanashri P., Ngo, Long H., Koralnik, Igor J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863751/
https://www.ncbi.nlm.nih.gov/pubmed/27231708
http://dx.doi.org/10.1002/acn3.301
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author Miskin, Dhanashri P.
Ngo, Long H.
Koralnik, Igor J.
author_facet Miskin, Dhanashri P.
Ngo, Long H.
Koralnik, Igor J.
author_sort Miskin, Dhanashri P.
collection PubMed
description We investigated delay in diagnosing progressive multifocal leukoencephalopathy (PML). The median time from initial symptom to diagnosis was 74 days (range 1–1643) in 111 PML patients seen at our institution from 1993 to 2015. Another diagnosis was considered before PML in nearly two–thirds, and more than three–quarters of patients suffered from diagnostic delay greater than 1 month, irrespective of their underlying immunosuppressive condition. Extended diagnostic delay occurred more frequently in patients with possible PML, and among HIV (+) patients with higher CD4(+) T‐cell counts at symptom onset. Prompt diagnosis may improve survival of PML in so far as immune reconstitution can be effected, and prevent unnecessary interventions.
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spelling pubmed-48637512016-05-26 Diagnostic delay in progressive multifocal leukoencephalopathy Miskin, Dhanashri P. Ngo, Long H. Koralnik, Igor J. Ann Clin Transl Neurol Brief Communications We investigated delay in diagnosing progressive multifocal leukoencephalopathy (PML). The median time from initial symptom to diagnosis was 74 days (range 1–1643) in 111 PML patients seen at our institution from 1993 to 2015. Another diagnosis was considered before PML in nearly two–thirds, and more than three–quarters of patients suffered from diagnostic delay greater than 1 month, irrespective of their underlying immunosuppressive condition. Extended diagnostic delay occurred more frequently in patients with possible PML, and among HIV (+) patients with higher CD4(+) T‐cell counts at symptom onset. Prompt diagnosis may improve survival of PML in so far as immune reconstitution can be effected, and prevent unnecessary interventions. John Wiley and Sons Inc. 2016-04-06 /pmc/articles/PMC4863751/ /pubmed/27231708 http://dx.doi.org/10.1002/acn3.301 Text en © 2016 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Brief Communications
Miskin, Dhanashri P.
Ngo, Long H.
Koralnik, Igor J.
Diagnostic delay in progressive multifocal leukoencephalopathy
title Diagnostic delay in progressive multifocal leukoencephalopathy
title_full Diagnostic delay in progressive multifocal leukoencephalopathy
title_fullStr Diagnostic delay in progressive multifocal leukoencephalopathy
title_full_unstemmed Diagnostic delay in progressive multifocal leukoencephalopathy
title_short Diagnostic delay in progressive multifocal leukoencephalopathy
title_sort diagnostic delay in progressive multifocal leukoencephalopathy
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863751/
https://www.ncbi.nlm.nih.gov/pubmed/27231708
http://dx.doi.org/10.1002/acn3.301
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