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Prevasculitic Eosinophilic Granulomatosis With Polyangiitis
Kathryn M Burtson1, Jonathan Bishop2
1Internal Medicine, Wright Patterson Air Force Base/Wright State University, Dayton, USA.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare vasculitis. This case highlights early identification of EGPA, which typically has a long diagnostic delay after asthma onset.
Area of Science:
- Rheumatology
- Pulmonology
- Immunology
Background:
- Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic necrotizing vasculitis.
- EGPA typically presents with asthma and eosinophilia, often with a significant diagnostic delay.
- Early diagnosis of EGPA is crucial for effective management.
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