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Eosinophilic granulomatosis with polyangiitis treatment

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare autoimmune disorder characterized by inflammation of blood vessels, often affecting the lungs, skin, and nerves. It involves an elevated number of eosinophils, a type of white blood cell, which can lead to tissue damage. Causes are not fully understood but may involve a combination of genetic and environmental factors. Treatment typically includes corticosteroids and immunosuppressive drugs to control inflammation and prevent organ damage. The response to treatment can vary, with improvements often seen within a few months. Dr. Sajal Ajmani provides expert management for EGPA, focusing on individualized treatment plans to control symptoms, prevent complications, and improve the patient's quality of life. Effective treatment can lead to significant symptom relief and improved overall health.

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