Systemic vasculitis are rare heterogeneous disorders potentially involving any organ and system with a relevant burden of mortality and comorbidity. As in the previous annual reviews of this series, in this review we will provide a critical digest of the most recent literature regarding pathophysiology, clinical manifestations, diagnostic tools and treatment options in small- and large-vessel vasculitis.

La Rocca, G., Del Frate, G., Delvino, P., Di Cianni, F., Moretti, M., Italiano, N., et al. (2022). Systemic vasculitis: one year in review 2022. CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 40(4), 673-687 [10.55563/clinexprheumatol/ozhc85].

Systemic vasculitis: one year in review 2022

Delvino P.;
2022

Abstract

Systemic vasculitis are rare heterogeneous disorders potentially involving any organ and system with a relevant burden of mortality and comorbidity. As in the previous annual reviews of this series, in this review we will provide a critical digest of the most recent literature regarding pathophysiology, clinical manifestations, diagnostic tools and treatment options in small- and large-vessel vasculitis.
Articolo in rivista - Review Essay
antineutrophil cytoplasmic antibody-associated vasculitis; cryoglobulinaemic vasculitis; eosinophilic granulomatosis with polyangiitis; giant cell arteritis; granulomatosis with polyangiitis; microscopic polyangiitis; systemic vasculitis; Takayasu’s arteritis;
English
4-mag-2022
2022
40
4
673
687
reserved
La Rocca, G., Del Frate, G., Delvino, P., Di Cianni, F., Moretti, M., Italiano, N., et al. (2022). Systemic vasculitis: one year in review 2022. CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 40(4), 673-687 [10.55563/clinexprheumatol/ozhc85].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/467453
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