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Published in: Current Rheumatology Reports 8/2013

01-08-2013 | VASCULITIS (LR ESPINOZA, SECTION EDITOR)

IgG4-Associated Vasculitis

Authors: Rodolfo Perez Alamino, Carlos Martínez, Luis R. Espinoza

Published in: Current Rheumatology Reports | Issue 8/2013

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Abstract

Elevated IgG4 is characteristic of cases of IgG4-RD, a newly recognized systemic disease. However, several chronic inflammatory conditions, including rheumatic diseases, can also be associated with increased levels of IgG4. There have also recently been several reports describing an increased IgG4 immune response to some vasculitis syndromes, in particular Churg–Strauss syndrome and granulomatosis with polyangiitis. To avoid misdiagnosis, clinicians must be aware that the clinical manifestations of IgG4-RD and ANCA-associated vasculitis may overlap. The meaning of these observations is not yet understood, and more studies are needed to determine the true significance of the increased IgG4 response to vasculitis syndromes, especially anti-neutrophil cytoplasmatic antibodies (ANCA)-associated vasculitis.
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Metadata
Title
IgG4-Associated Vasculitis
Authors
Rodolfo Perez Alamino
Carlos Martínez
Luis R. Espinoza
Publication date
01-08-2013
Publisher
Springer US
Published in
Current Rheumatology Reports / Issue 8/2013
Print ISSN: 1523-3774
Electronic ISSN: 1534-6307
DOI
https://doi.org/10.1007/s11926-013-0348-9

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