Journal ArticleOPEN ACCESS

Polyclonal hyperviscosity syndrome in IgG4‐related disease and associated conditions

  • Chen L
  • Wong P
  • Noda S
  • et al.
Clinical Case Reports (2015) 3(4) 217-226
DOI: 10.1002/ccr3.201
N/ACitations
Citations of this article
21Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

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 .

Cite

CITATION STYLE

APA

Chen, L. Y. C., Wong, P. C. W., Noda, S., Collins, D. R., Sreenivasan, G. M., & Coupland, R. C. (2015). Polyclonal hyperviscosity syndrome in IgG4‐related disease and associated conditions. Clinical Case Reports, 3(4), 217–226. https://doi.org/10.1002/ccr3.201

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free