Approaches to Diagnosis and Management of Microscopic Polyangiitis
medscape.com
Approaches to Diagnosis and Management of Microscopic Polyangiitis
Early diagnosis of microscopic polyangiitis is critical to prevent organ damage, and newer therapies that involve complement inhibition can spare patients from glucocorticoid treatment side effects.
6 months ago
Microscopic Polyangiitis Symptoms
Eosinophilic granulomatosis with polyangiitis or EGPA, is a form of vasculitis – a family of rare diseases characterized by inflammation of blood vessels, which can restrict blood flow and damage vital organs and tissues. Anyone can get EGPA, but it’s most common in men and women ages 35-50. To learn more about this serious, yet treatable disease, visit Lung.org/EGPA | American Lung Association
0:16
Eosinophilic granulomatosis with polyangiitis or EGPA, is a form of vasculitis – a family of rare diseases characterized by inflammation of blood vessels, which can restrict blood flow and damage vital organs and tissues. Anyone can get EGPA, but it’s most common in men and women ages 35-50. To learn more about this serious, yet treatable disease, visit Lung.org/EGPA | American Lung Association
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Microscopic Polyangiitis Treatment
Qbankmedicine on Instagram: "Answer with Explanation : ✅ Correct Answer: B. Polyarteritis nodosa Explanation: Polyarteritis nodosa causes necrotizing inflammation of medium-sized arteries, including mesenteric arteries, leading to intestinal ischemia and post-prandial abdominal pain (intestinal angina). Why the other options are incorrect: A. Microscopic polyangiitis → Small-vessel vasculitis, usually causes glomerulonephritis and pulmonary hemorrhage C. Granulomatosis with polyangiitis → ENT +
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Qbankmedicine on Instagram: "Answer with Explanation : ✅ Correct Answer: B. Polyarteritis nodosa Explanation: Polyarteritis nodosa causes necrotizing inflammation of medium-sized arteries, including mesenteric arteries, leading to intestinal ischemia and post-prandial abdominal pain (intestinal angina). Why the other options are incorrect: A. Microscopic polyangiitis → Small-vessel vasculitis, usually causes glomerulonephritis and pulmonary hemorrhage C. Granulomatosis with polyangiitis → ENT +
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Eosinophilic granulomatosis with polyangiitis or EGPA, is a form of vasculitis – a family of rare diseases characterized by inflammation of blood vessels, which can restrict blood flow and damage vital organs and tissues. Anyone can get EGPA, but it’s most common in men and women ages 35-50. To learn more about this serious, yet treatable disease, visit Lung.org/EGPA | American Lung Association
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