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Clin Case Rep ; 3(4): 217-26, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25914812

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.

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