Déjà vu. (PubMed, BMJ Case Rep) - Sep 17, 2026 - "Treatment with corticosteroids, rituximab and anticoagulation resulted in sustained remission over 36 months. This case highlights the diagnostic continuum between HES and EGPA and the need for long-term follow-up with reassessment of diagnosis. Early recognition of evolving vasculitis is essential to guide appropriate immunosuppressive therapy."
Journal • Cardiovascular • Eosinophilia • Eosinophilic Granulomatosis With Polyangiitis • Hematological Disorders • Hepatology • Hypereosinophilic Syndrome • Immunology • Langerhans Cell Histiocytosis • Liver Failure • Pain • Rare Diseases • Rheumatology • Thrombosis • Vasculitis
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Aashish Omprakash Agrawal; Aditi Sanjiv Patankar; Rohini Samant
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