One year in review 2018: systemic vasculitis

Clin Exp Rheumatol. 2018 Mar-Apr;36 Suppl 111(2):12-32. Epub 2018 May 18.

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.

Publication types

  • Review

MeSH terms

  • Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis / drug therapy
  • Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis / immunology
  • Antirheumatic Agents / therapeutic use
  • Churg-Strauss Syndrome / drug therapy
  • Churg-Strauss Syndrome / immunology
  • Cryoglobulinemia / complications
  • Cryoglobulinemia / drug therapy
  • Cryoglobulinemia / immunology*
  • Giant Cell Arteritis / drug therapy
  • Giant Cell Arteritis / immunology
  • Granulomatosis with Polyangiitis / drug therapy
  • Granulomatosis with Polyangiitis / immunology
  • Hepatitis C, Chronic / complications
  • Hepatitis C, Chronic / immunology*
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Microscopic Polyangiitis / drug therapy
  • Microscopic Polyangiitis / immunology
  • Systemic Vasculitis / drug therapy
  • Systemic Vasculitis / etiology
  • Systemic Vasculitis / immunology*
  • Takayasu Arteritis / drug therapy
  • Takayasu Arteritis / immunology

Substances

  • Antirheumatic Agents
  • Immunosuppressive Agents