A novel clinical entity, IgG4-related disease (IgG4RD): general concept and details
By H. Umehara, K. Okazaki, Y. Masaki, M. Kawano, M. Yamamoto, T. Saeki, Shoko Matsui, T. Sumida, T. Mimori, Yoshiya Tanaka and 12 more. Modern Rheumatology, 2011
650 citations recorded by the source corpus.
IgG4-related disease (IgG4RD) is a novel clinical disease entity characterized by elevated serum IgG4 concentration and tumefaction or tissue infiltration by IgG4-positive plasma cells. IgG4RD may be present in a certain proportion of patients with a wide variety of diseases, including Mikulicz’s disease, autoimmune pancreatitis, hypophysitis, Riedel thyroiditis, interstitial pneumonitis, interstitial nephritis, prostatitis, lymphadenopathy, retroperitoneal fibrosis, inflammatory aortic aneurysm, and inflammatory pseudotumor. Although IgG4RD forms a distinct, clinically independent disease category and is attracting strong attention as a new clinical entity, many questions and problems still remain to be elucidated, including its pathogenesis, the establishment of diagnostic criteria, and the role of IgG4. Here we describe the concept of IgG4RD and up-to-date information on this emerging disease entity.
Subfields: Epidemiology, Rheumatology, Surgery
View Paper: https://www.semanticscholar.org/paper/ba84a8a32150c908fca5a7ac1a450bdc9d8e5ac4
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- Shoko Matsui
- Shigeo Nakamura
- T. Shimosegawa
- A. Shimatsu
- Seiji Nakamura
- Tetsuhide Ito
- T. Hibi
- H. Hamano
Citations in the corpus
- Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011 (2012, background): “The common characteristics of these conditions include elevated serum IgG4 concentrations and tissue infiltration by IgG4? plasma cells, accompanied by tissue fibrosis and sclerosis [1].”