| Literature DB >> 28623488 |
Benjamin Chaigne1, Loïc Guillevin2.
Abstract
Vasculitides comprise several diseases affecting vessels of different sizes, mainly arteries, but also capillaries and veins. Antineutrophil cytoplasm antibody-associated vasculitides (AAVs) belong to the systemic necrotizing small-vessel vasculitis group that comprises granulomatosis with polyangiitis, microscopic polyangiitis and eosinophilic granulomatosis with polyangiitis. Internists often see AAV patients, and although their outcomes are usually good, the disease can be responsible for morbidity and mortality. Herein, after reviewing the literature, we concentrate on selected aspects important for the internist, including classification, diagnostic dilemmas, treatment novelties, and follow-up.Entities:
Keywords: ANCA; EGPA; GPA; HRQoL; MPA; Rituximab; Vasculitis
Mesh:
Substances:
Year: 2017 PMID: 28623488 DOI: 10.1007/s11739-017-1683-z
Source DB: PubMed Journal: Intern Emerg Med ISSN: 1828-0447 Impact factor: 3.397