Systemic vasculitis is a group of heterogeneous, disabling disorders. Great interest has recently arisen in pathophysiology, clinical phenotypes and therapy of large- and small-vessel vasculitis. The general work hypothesis has been to promote research focused on disease-related pathogenetic pathways, with the ultimate goal of identifying novel diagnostic and prognostic biomarkers, thus leading towards more effective targeted treatments. Following the previous annual reviews of this series, we will hereby provide a critical digest of the recent literature on small and large-vessel systemic vasculitis, with a specific focus on novel possible disease-related biomarkers and their impact on current and future therapies.

One year in review 2017: systemic vasculitis / E. Elefante, S. Monti, M. Bondi, G. Lepri, L. Quartuccio, R. Talarico, C. Baldini. - In: CLINICAL AND EXPERIMENTAL RHEUMATOLOGY. - ISSN 0392-856X. - 35:1, suppl. 103(2017), pp. S5-S26.

One year in review 2017: systemic vasculitis

S. Monti
Secondo
;
2017

Abstract

Systemic vasculitis is a group of heterogeneous, disabling disorders. Great interest has recently arisen in pathophysiology, clinical phenotypes and therapy of large- and small-vessel vasculitis. The general work hypothesis has been to promote research focused on disease-related pathogenetic pathways, with the ultimate goal of identifying novel diagnostic and prognostic biomarkers, thus leading towards more effective targeted treatments. Following the previous annual reviews of this series, we will hereby provide a critical digest of the recent literature on small and large-vessel systemic vasculitis, with a specific focus on novel possible disease-related biomarkers and their impact on current and future therapies.
ANCA vasculitis; Cryoglobulinaemia; Giant cell arteritis; Systemic vasculitis; Takayasu arteritis
Settore MEDS-09/C - Reumatologia
2017
https://www.clinexprheumatol.org/article.asp?a=11676
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1167705
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