Microscopic polyangiitis case study

Short essay description
Granulomatosis with Polyangiitis is nearly equally distributed between the sexes, with a slight male predominance. Granulomatosis with Polyangiitis typically occurs in middle age, but is found in people of all ages. Pictured below is a chest x—ray showing bilateral lung nodules in a 27 year old Indian man with Granulomatosis with Polyangiitis. Pictured below is a CT scan from the same patient. Granulomatosis with Polyangiitis can affect virtually any site in the body, but it has a predisposition for certain organs.
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Microscopic polyangiitis

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Remission Induction Therapy with Rituximab for Microscopic Polyangiitis: A Feasibility Study

Metrics details. MPA patients with renal involvement may have a worse prognosis. In this study, we aimed to evaluate the prognostic factors associated with all-cause death and renal survival in MPA patients with renal involvement. A retrospective observational cohort study was performed.
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Renal Artery Rupture a Rare Complication of Microscopic Polyangiitis, Case Study Reports

Microscopic polyangiitis MPA is a systemic vasculitis involving small- and medium-sized vessels and is associated with a focal and segmental necrotizing glomerulonephritis. MPA may be characterized as a pulmonary-renal syndrome with rapidly progressive glomerulonephritis and alveolar hemorrhage; however, the manifestations of the disease vary depending on the organ systems involved 1. The incidence and diagnosis rates of vasculitis have recently been rising constantly. The detection of ANCA in the serum has therefore become an important basis for the diagnosis of vasculitis 3. ANCA-negative vasculitis is relatively rare and is thus prone to misdiagnosis.
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Metrics details. The association between a preceding malignancy and the onset of anti-neutrophil cytoplasmic antibody ANCA -associated vasculitis AAV has been reported in several studies. While the co-existence of ANCA and anti-glomerular basement membrane GBM antibodies in an individual patient is not a common occurrence, this double-positive disease currently has no optimal treatment method.
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