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A case of vanishing bile duct syndrome during treatment of microscopic polyangiitis with avacopan.
Rheumatology, 2023Satoshi Yamaguchi +8 more
semanticscholar +1 more source
Propylthiouracil-Induced Microscopic Polyangiitis
JCR: Journal of Clinical Rheumatology, 2001The use of propylthiouracil (PTU) has been associated with various forms of vasculitis. We herein describe the case of a patient with Grave's disease who, after years of PTU therapy, developed a necrotizing vasculitis with anti-serine protease-3 antibodies.
V A, Seligman +3 more
openaire +2 more sources
Microscopic polyangiitis: Clinical presentation
Autoimmunity Reviews, 2010Microscopic polyangiitis (MPA) is a member of the family of ANCA-associated vasculitides. Its characteristic histology shows a necrotizing small vessel vasculitis with little or absent immune deposits (pauci-immune vasculitis). In Western countries MPA shows a lower prevalence than Wegener's disease, it affects more men than women and commences at the ...
Peter M, Villiger, Loïc, Guillevin
openaire +2 more sources
European Cytokine Network, 2019
Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is an autoimmune disorder of unknown etiology with dysregulated cytokines levels.
Joanna Krajewska (Wojciechowska) +3 more
semanticscholar +1 more source
Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is an autoimmune disorder of unknown etiology with dysregulated cytokines levels.
Joanna Krajewska (Wojciechowska) +3 more
semanticscholar +1 more source
La Revue du praticien, 2002
Microscopic polyangiitis is a systemic necrotizing vasculitis affecting small vessels, without granulomata. Patients present with rapidly progressive glomerulonephritis, often associated with cutaneous, musculoskeletal, neurological or gastrointestinal involvement. Antineutrophilcytoplasmic antibodies are frequently found, most often with a perinuclear
D, Lauque, J, Pourrat
openaire +1 more source
Microscopic polyangiitis is a systemic necrotizing vasculitis affecting small vessels, without granulomata. Patients present with rapidly progressive glomerulonephritis, often associated with cutaneous, musculoskeletal, neurological or gastrointestinal involvement. Antineutrophilcytoplasmic antibodies are frequently found, most often with a perinuclear
D, Lauque, J, Pourrat
openaire +1 more source
Epidemiology of granulomatosis with polyangiitis and microscopic polyangiitis in adults in France.
Journal of Autoimmunity, 2022P. Bataille +5 more
semanticscholar +1 more source