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Neurological aspects of human parvovirus B19 infection: a systematic review

Parvovirus B19 has been linked with various clinical syndromes including neurological manifestations. However, its role in the latter remains not completely understood. Although the last 10 years witnessed a surge of case reports on B19-associated neurological aspects, the literature data remains sc...

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Autores principales: Barah, Faraj, Whiteside, Sigrid, Batista, Sonia, Morris, Julie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238837/
https://www.ncbi.nlm.nih.gov/pubmed/24459081
http://dx.doi.org/10.1002/rmv.1782
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author Barah, Faraj
Whiteside, Sigrid
Batista, Sonia
Morris, Julie
author_facet Barah, Faraj
Whiteside, Sigrid
Batista, Sonia
Morris, Julie
author_sort Barah, Faraj
collection PubMed
description Parvovirus B19 has been linked with various clinical syndromes including neurological manifestations. However, its role in the latter remains not completely understood. Although the last 10 years witnessed a surge of case reports on B19-associated neurological aspects, the literature data remains scattered and heterogeneous, and epidemiological information on the incidence of B19-associated neurological aspects cannot be accurately extrapolated. The aim of this review is to identify the characteristics of cases of B19-associated neurological manifestations. A computerized systematic review of existing literature concerning cases of B19-related neurological aspects revealed 89 articles describing 129 patients; 79 (61.2%) were associated with CNS manifestations, 41 (31.8%) were associated with peripheral nervous system manifestations, and 9 (7.0%) were linked with myalgic encephalomyelitis. The majority of the cases (50/129) had encephalitis. Clinical characteristic features of these cases were analyzed, and possible pathological mechanisms were also described. In conclusion, B19 should be included in differential diagnosis of encephalitic syndromes of unknown etiology in all age groups. Diagnosis should rely on investigation of anti-B19 IgM antibodies and detection of B19 DNA in serum or CSF. Treatment of severe cases might benefit from a combined regime of intravenous immunoglobulins and steroids. To confirm these outcomes, goal-targeted studies are recommended to exactly identify epidemiological scenarios and explore potential pathogenic mechanisms of these complications. Performing retrospective and prospective and multicenter studies concerning B19 and neurological aspects in general, and B19 and encephalitic syndromes in particular, are required. © 2014 The Authors. Reviews in Medical Virology published by John Wiley & Sons, Ltd.
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spelling pubmed-42388372014-11-28 Neurological aspects of human parvovirus B19 infection: a systematic review Barah, Faraj Whiteside, Sigrid Batista, Sonia Morris, Julie Rev Med Virol Review Parvovirus B19 has been linked with various clinical syndromes including neurological manifestations. However, its role in the latter remains not completely understood. Although the last 10 years witnessed a surge of case reports on B19-associated neurological aspects, the literature data remains scattered and heterogeneous, and epidemiological information on the incidence of B19-associated neurological aspects cannot be accurately extrapolated. The aim of this review is to identify the characteristics of cases of B19-associated neurological manifestations. A computerized systematic review of existing literature concerning cases of B19-related neurological aspects revealed 89 articles describing 129 patients; 79 (61.2%) were associated with CNS manifestations, 41 (31.8%) were associated with peripheral nervous system manifestations, and 9 (7.0%) were linked with myalgic encephalomyelitis. The majority of the cases (50/129) had encephalitis. Clinical characteristic features of these cases were analyzed, and possible pathological mechanisms were also described. In conclusion, B19 should be included in differential diagnosis of encephalitic syndromes of unknown etiology in all age groups. Diagnosis should rely on investigation of anti-B19 IgM antibodies and detection of B19 DNA in serum or CSF. Treatment of severe cases might benefit from a combined regime of intravenous immunoglobulins and steroids. To confirm these outcomes, goal-targeted studies are recommended to exactly identify epidemiological scenarios and explore potential pathogenic mechanisms of these complications. Performing retrospective and prospective and multicenter studies concerning B19 and neurological aspects in general, and B19 and encephalitic syndromes in particular, are required. © 2014 The Authors. Reviews in Medical Virology published by John Wiley & Sons, Ltd. BlackWell Publishing Ltd 2014-05 2014-01-24 /pmc/articles/PMC4238837/ /pubmed/24459081 http://dx.doi.org/10.1002/rmv.1782 Text en © 2014 The Authors. Reviews in Medical Virology published by John Wiley & Sons, Ltd. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review
Barah, Faraj
Whiteside, Sigrid
Batista, Sonia
Morris, Julie
Neurological aspects of human parvovirus B19 infection: a systematic review
title Neurological aspects of human parvovirus B19 infection: a systematic review
title_full Neurological aspects of human parvovirus B19 infection: a systematic review
title_fullStr Neurological aspects of human parvovirus B19 infection: a systematic review
title_full_unstemmed Neurological aspects of human parvovirus B19 infection: a systematic review
title_short Neurological aspects of human parvovirus B19 infection: a systematic review
title_sort neurological aspects of human parvovirus b19 infection: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238837/
https://www.ncbi.nlm.nih.gov/pubmed/24459081
http://dx.doi.org/10.1002/rmv.1782
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