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Eosinophilic Granulomatosis with Polyangiitis
Ratnakar Shukla1, Ashwini Kandikatla2, Nitin J Nadkarni3
1Department of Dermatology, All India Institute of Medical Sciences, Gorakhpur, Uttar Pradesh, India.
This report details a rare case of Eosinophilic Granulomatosis with Polyangiitis (EGPA), also known as Churg-Strauss syndrome, in a 58-year-old male. The patient presented with lower limb swelling and skin lesions, highlighting EGPA
Area of Science:
- Rheumatology
- Immunology
- Dermatology
Background:
- Eosinophilic Granulomatosis with Polyangiitis (EGPA), or Churg-Strauss syndrome, is a rare systemic necrotizing vasculitis affecting small-to-medium-sized vessels.
- EGPA is characterized by asthma, hypereosinophilia, and systemic vasculitis.
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