[PDF][PDF] Epidemiological study of primary systemic vasculitides among adults in southern Spain and review of the main epidemiological studies

C Romero-Gómez, JA Aguilar-García… - Clin Exp …, 2015 - clinexprheumatol.org
Objective. To study the incidence and prevalence of primary systemic vasculitides (PSV) in
the Costa del Sol region (southern Spain) and to compare the major epidemiological studies …

[HTML][HTML] Pathophysiology and therapy of systemic vasculitides

M Ralli, F Campo, D Angeletti, A Minni, M Artico… - EXCLI …, 2020 - ncbi.nlm.nih.gov
Systemic vasculitides represent uncommon conditions characterized by the inflammation of
blood vessels that can lead to different complex disorders limited to one organ or potentially …

Granulomatosis with polyangiitis: study of 795 patients from the French Vasculitis Study Group registry

M Iudici, C Pagnoux, DS Courvoisier, P Cohen… - Seminars in Arthritis and …, 2021 - Elsevier
Objective To describe the characteristics and long-term outcomes of patients with
granulomatosis with polyangiitis (GPA) from the French Vasculitis Study Group database …

A review of anti-IL-5 therapies for eosinophilic granulomatosis with polyangiitis

H Koike, R Nishi, S Yagi, S Furukawa, Y Fukami… - Advances in …, 2023 - Springer
Eosinophilic granulomatosis with polyangiitis (EGPA), previously known as Churg–Strauss
syndrome, is a systemic disorder characterized by asthma, eosinophilia, and vasculitis …

ANCA associated vasculitis

F Salvador - European Journal of Internal Medicine, 2020 - Elsevier
Vasculitis is characterized by inflammation of the vascular wall. It reaches vessels of different
sizes and locations, conditioning multisystem and complex manifestations that require a …

Diagnosing and treating ANCA-associated vasculitis: an updated review for clinical practice

B Chevet, D Cornec, M Casal Moura… - …, 2023 - academic.oup.com
ANCA-associated vasculitides (AAV) are a group of rare, primary, systemic necrotizing small-
vessel vasculitides. Granulomatosis with polyangiitis and microscopic polyangiitis account …

Granulomatosis with polyangiitis (Wegener's granulomatosis): evolving concepts in treatment

JP Lynch III, A Derhovanessian… - … in respiratory and …, 2018 - thieme-connect.com
Granulomatosis with polyangiitis (GPA), formerly termed Wegener's granulomatosis, is the
most common of the pulmonary vasculitides. GPA typically involves the upper respiratory …

The epidemiology of Wegener's granulomatosis and microscopic polyangiitis in a Southern Hemisphere region

A Gibson, LK Stamp, PT Chapman… - Rheumatology, 2006 - academic.oup.com
Objective. To determine the prevalence of Wegener's granulomatosis (WG) and microscopic
polyangiitis (MPA) in the province of Canterbury, New Zealand. Method. Three hospital …

Polyarteritis nodosa

L Forbess, S Bannykh - Rheumatic Disease Clinics, 2015 - rheumatic.theclinics.com
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis, which typically affects
medium-sized muscular arteries, particularly affecting the visceral, renal, and soft tissue …

Renal granulomatoses: a retrospective study of 40 cases and review of the literature

N Javaud, X Belenfant, J Stirnemann, J Laederich… - Medicine, 2007 - journals.lww.com
Abstract Renal granulomatoses represent 0.5%-0.9% of nephropathies examined by renal
biopsies. Granulomas can be isolated to the kidney or associated with other tissue …