Results 111 to 120 of about 331,732 (145)
Microscopic Polyangiitis in a Pregnant Woman
Southern Medical Journal, 2002 Patients who have vasculitis in pregnancy generally have a grim prognosis. Vasculitis occurring during pregnancy may have a more aggressive course and require more aggressive treatment than vasculitis occurring at other times. A 29-year-old woman who presented in the 16th week of her third intrauterine pregnancy was diagnosed as having active ...
Keles, Muzaffer +6 more
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Microscopic polyangiitis: Advances in diagnostic and therapeutic approaches
Autoimmunity Reviews, 2015 Microscopic polyangiitis (MPA) is an idiopathic autoimmune disease characterized by systemic vasculitis. The disease predominantly affects small-calibre blood vessels and is associated with the presence of antineutrophil cytoplasmic autoantibodies (ANCA).
Andrea Gallo +2 more
exaly +2 more sources
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Presse medicale (Paris, France : 1983), 2007
Microscopic polyangiitis was initially considered a "microscopic" form of polyarteritis nodosa and was not definitively distinguished from it until the Chapel Hill nomenclature (1994). Microscopic polyangiitis is a systemic necrotizing vasculitis of small vessels.
Christian, Pagnoux +2 more
openaire +3 more sources
Microscopic polyangiitis was initially considered a "microscopic" form of polyarteritis nodosa and was not definitively distinguished from it until the Chapel Hill nomenclature (1994). Microscopic polyangiitis is a systemic necrotizing vasculitis of small vessels.
Christian, Pagnoux +2 more
openaire +3 more sources
[Granulomatosis with polyangiitis and microscopic polyangiitis].
Laryngo- rhino- otologieGranulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) are two entities of ANCA-associated vasculitis (AAV). Both diseases are characterised by systemic necrotising small-vessel vasculitis, which can affect any organ. In GPA, extravascular necrotising granulomatous inflammation, usually affecting the respiratory tract, is found in ...
Sebastian, Klapa +2 more
openaire +1 more source
2019
Microscopic polyangiitis (MPA) is a pauci-immune necrotizing small vessel vasculitis in which necrotizing crescentic glomerulonephritis (GN) is very common and pulmonary capillaritis often occurs. It belongs to the group of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis and can be differentiated from granulomatosis with polyangiitis (
SINICO, RENATO ALBERTO +4 more
openaire +2 more sources
Microscopic polyangiitis (MPA) is a pauci-immune necrotizing small vessel vasculitis in which necrotizing crescentic glomerulonephritis (GN) is very common and pulmonary capillaritis often occurs. It belongs to the group of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis and can be differentiated from granulomatosis with polyangiitis (
SINICO, RENATO ALBERTO +4 more
openaire +2 more sources
Annales de medecine interne, 2000
Microscopic polyangiitis is a non-granulomatous necrotizing vasculitis involving small vessels. Clinical manifestations are highly polymorphic, but rapidly progressive glomerulonephritis is one of the most frequent and most severe manifestations of the disease.
J P, Venetz, J, Rossert
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Microscopic polyangiitis is a non-granulomatous necrotizing vasculitis involving small vessels. Clinical manifestations are highly polymorphic, but rapidly progressive glomerulonephritis is one of the most frequent and most severe manifestations of the disease.
J P, Venetz, J, Rossert
openaire +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