hypergammaglobulinemia


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Translations

hy·per·gam·ma·glob·u·lin·e·mi·a

n. hipergammaglobulinemia, exceso de gamma globulina en la sangre.
References in periodicals archive ?
Furthermore, there is a relationship between the number of systemic autoantibodies and the number of EGM in pSS with a high prevalence of anti-Sjogren syndrome A antigen, anti-Sjogren syndrome B antigen, anti-nuclear antibodies, and immunoglobulin M-rheumatoid factor antibodies, indicating that a more disturbed immune system (as characterized by the presence of hypergammaglobulinemia and multiple autoantibodies formed by hyper-reactive B-cells) may result in more EGM.
AIP was first described in 1961 by Sarles et al as pancreatitis with hypergammaglobulinemia.
AITL is a rare hematologic disease that classically presents with lymphadenopathy, hepatosplenomegaly, hypergammaglobulinemia, anemia, and B-type symptoms and is distinguished by distinctive lymph node architecture disruption.
Hypo complementemia due to complement cascade activation is common, as well as hypergammaglobulinemia due to polyclonal B lymphocyte expansion.
Solitary crystal-storing histiocytosis of the tongue in a patient with rheumatoid arthritis and polyclonal hypergammaglobulinemia.
72 Waldenstrom's hypergammaglobulinemia 9069 Pipeline and Portfolio Planning: Competitive Benchmarking of the Cancer Antibody Drug Pipeline by Investigator 9089.
Clinical characteristics often include a painless cervicallymphadenopathy, fever, leukocytosis, an elevated erythrocyte sedimentation rate, and polyclonal hypergammaglobulinemia.
In humans with B-cell CLL, monoclonal hypergammaglobulinemia can occur.
In patients with polyclonal hypergammaglobulinemia (as determined by serum protein electrophoresis and immunofixation electrophoresis), nonspecific increases in FLCs occurred in a fashion similar to the nonspecific increases in CRP seen with inflammation.
14) In Woulters et al's study, all JIA patients had hypergammaglobulinemia consistent with B cell hyperactivity.
Laboratory test results show marked eosinophilia, anemia, hypergammaglobulinemia, and increased titers to A and B blood group antigens.