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Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions
Polyclonal hyperviscosity syndrome (HVS) is rare and has been reported in various disorders of immune dysregulation and lymphoid hyperplasia. IgG4-Related Disease (IgG4-RD) is an emerging disorder often associated with exuberant hypergammaglobulinemia, and this review of seven cases establishes IgG4...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405305/ https://www.ncbi.nlm.nih.gov/pubmed/25914812 http://dx.doi.org/10.1002/ccr3.201 |
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author | Chen, Luke YC Wong, Patrick CW Noda, Shinji Collins, David R Sreenivasan, Gayatri M Coupland, Robert C |
author_facet | Chen, Luke YC Wong, Patrick CW Noda, Shinji Collins, David R Sreenivasan, Gayatri M Coupland, Robert C |
author_sort | Chen, Luke YC |
collection | PubMed |
description | Polyclonal hyperviscosity syndrome (HVS) is rare and has been reported in various disorders of immune dysregulation and lymphoid hyperplasia. IgG4-Related Disease (IgG4-RD) is an emerging disorder often associated with exuberant hypergammaglobulinemia, and this review of seven cases establishes IgG4-RD as an important cause of polyclonal HVS. |
format | Online Article Text |
id | pubmed-4405305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44053052015-04-24 Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions Chen, Luke YC Wong, Patrick CW Noda, Shinji Collins, David R Sreenivasan, Gayatri M Coupland, Robert C Clin Case Rep Case Reports Polyclonal hyperviscosity syndrome (HVS) is rare and has been reported in various disorders of immune dysregulation and lymphoid hyperplasia. IgG4-Related Disease (IgG4-RD) is an emerging disorder often associated with exuberant hypergammaglobulinemia, and this review of seven cases establishes IgG4-RD as an important cause of polyclonal HVS. BlackWell Publishing Ltd 2015-04 2015-02-02 /pmc/articles/PMC4405305/ /pubmed/25914812 http://dx.doi.org/10.1002/ccr3.201 Text en © 2015 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 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 | Case Reports Chen, Luke YC Wong, Patrick CW Noda, Shinji Collins, David R Sreenivasan, Gayatri M Coupland, Robert C Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions |
title | Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions |
title_full | Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions |
title_fullStr | Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions |
title_full_unstemmed | Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions |
title_short | Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions |
title_sort | polyclonal hyperviscosity syndrome in igg4-related disease and associated conditions |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405305/ https://www.ncbi.nlm.nih.gov/pubmed/25914812 http://dx.doi.org/10.1002/ccr3.201 |
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