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Eosinophilic granulomatosis with polyangiitis (EGPA), formerly Churg–Strauss syndrome, is a rare autoimmune disease characterized by asthma, high eosinophil levels, and systemic vasculitis affecting small- to medium-sized blood vessels. The disease progresses through three phases: allergic, eosinophilic, and vasculitic, with treatment options including corticosteroids, immunosuppressants, and targeted therapy. Early diagnosis is crucial for preventing organ damage and improving prognosis, particularly in ca

Author

nickgwards

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EN