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Eosinophilic Granulomatosis With Polyangiitis: A Case Report.
Ciji Robinson1, Jasdeep S Minhas2, Abraham Kisule3
1Internal Medicine, Henry Ford Health System, Jackson, USA.
Cureus
|May 14, 2024
Summary
Eosinophilic granulomatosis with polyangiitis (EGPA), a rare vasculitis, can present with neurological symptoms. This case highlights the diagnostic challenges and successful steroid treatment for EGPA in an adult male with asthma.
Area of Science:
- Medicine
- Rheumatology
- Neurology
Background:
- Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis.
- EGPA is characterized by asthma, eosinophilia, and ANCA positivity.
- Diagnosis can be challenging due to varied presentations.

