Results 31 to 40 of about 8,090 (217)
Linked help from bacterial proteins drives autoantibody production in small vessel vasculitis. [PDF]
, 2018 The small vessel vasculitides granulomatosis with polyangiitis (GPA) and microscopic polyangiitis are associated with autoantibodies to neutrophil cytoplasm antigens (ANCA), principally proteinase-3 (PR3) and myeloperoxidase (MPO).
Oliveira, DBG
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Fulminant Wegener's granulomatosis: A case report [PDF]
, 2013 Introduction. Granulomatosis Wegener is anti-neutrophil cytoplasmic antibodies (ANCAs)-associated systemic vasculitis of unknown etiology. It is manifested as granulomatous necrotizing inflammation of the upper and lower parts of the respiratory tract,
Dinić Miroslav Ž. +3 more
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Wegener's granulomatosis [PDF]
, 2009 This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and therapeutics of Wegener's ...
Grine, Kristen, Jansen, Matthew
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Clinical Medicine Insights: Case Reports, 2009 Wegener's granulomatosis is a granulomatous necrotizing vasculitis characterized by its predilection to affect the upper and lower respiratory tracts and kidneys.
Brian Bowers +3 more
doaj +1 more source
Wegener's Granulomatosis presenting with an abscess in the parotid gland: a case report
Journal of Medical Case Reports, 2009 Introduction Wegener's Granulomatosis is a vasculitis of uncertain aetiology. Affected patients usually present with disease of the respiratory and renal tracts.
Geyer Marcel +2 more
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Association of ANCA associated vasculitis and rheumatoid arthritis: a lesser recognized overlap syndrome [PDF]
, 2015 Background ANCA associated vasculitis (AAV) is an autoimmune disease with significant morbidity and mortality, in which diagnostic delay is associated with worse outcomes. AAV is rarely found in association with other immune mediated diseases.
Draibe, J, Salama, AD
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Journal of Medical Case Reports, 2012 Introduction Wegener’s granulomatosis presenting as diffuse alveolar hemorrhage is uncommon. However, the recognition of multisystem disease involving joints, kidney, eye and lung is critical for diagnosing Wegener's vasculitis.
Cardenas-Garcia Jose +3 more
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An unusual case of granulomatosis with polyangiitis with unilateral parotid gland enlargement
Clinical Case Reports, 2023 Key Clinical Message Here, we report a case of granulomatosis with polyangiitis presenting with unilateral parotid gland enlargement and later developed skin lesions on the lower extremities and abdomen.
Toktam Safari Giv +4 more
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Wegener's granulomatosis [PDF]
British Journal of Ophthalmology, 2003 Wegener's granulomatosis (WG) is a systemic granulomatous inflammatory disease of unknown origin. It occurs at any age, with the peak incidence in the third and fourth decades. The classic diagnostic triad of WG is necrotising granuloma of the upper or lower respiratory tract, vasculitis, and nephritis.
K S, Lim +3 more
openaire +2 more sources
Туберкулез и болезни лёгких, 2023 The article describes a clinical case of Wegener's granulomatosis, which manifested in the post-COVID period in a young man; also it discusses diagnostic difficulties.
B. E. Borodulin +4 more
doaj +1 more source