Systemic vasculitis are heterogeneous, complex and disabling disorders. Following the previous annual reviews of this series, this paper gives a brief overview on current knowledge about recent literature on small- and large-vessel systemic vasculitis, with a specific focus on pathogenetic and clinical aspects, novel possible disease-related biomarkers and current and future therapies that are in the pipeline.

One year in review 2018: systemic vasculitis / E. Elefante, M. Bond, S. Monti, G. Lepri, E. Cavallaro, M. Felicetti, E. Calabresi, C. Posarelli, R. Talarico, L. Quartuccio, C. Baldini. - In: CLINICAL AND EXPERIMENTAL RHEUMATOLOGY. - ISSN 0392-856X. - 36:2, suppl. 111(2018), pp. S12-S32.

One year in review 2018: systemic vasculitis

S. Monti;
2018

Abstract

Systemic vasculitis are heterogeneous, complex and disabling disorders. Following the previous annual reviews of this series, this paper gives a brief overview on current knowledge about recent literature on small- and large-vessel systemic vasculitis, with a specific focus on pathogenetic and clinical aspects, novel possible disease-related biomarkers and current and future therapies that are in the pipeline.
vasculitis; giant cell arteritis; Takayasu’s arteritis; antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis; microscopic polyangiitis; granulomatosis with polyangiitis; eosinophilic granulomatosis with polyangiitis; HCV-related cryoglobulinaemia
Settore MEDS-09/C - Reumatologia
2018
https://www.clinexprheumatol.org/article.asp?a=12964
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1167698
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