Eosinophilic Granulomatosis With Polyangiitis Presenting With Rare Neurological Manifestations. (PubMed, Case Rep Neurol Med) - Sep 17, 2026 - "The patient was treated with high-dose corticosteroids and rituximab, resulting in significant clinical and biochemical improvement at 3 months. This case illustrates the coexistence of atypical neurological manifestations of EGPA, including prominent myopathy, length-dependent polyneuropathy, and retrospectively suspected central nervous system vasculitic involvement, emphasizing the importance of early recognition and multidisciplinary management."
Journal • ANCA Vasculitis • Asthma • Eosinophilia • Eosinophilic Granulomatosis With Polyangiitis • Immunology • Inflammation • Langerhans Cell Histiocytosis • Musculoskeletal Pain • Myositis • Pain • Pulmonary Disease • Rare Diseases • Respiratory Diseases • Rheumatology • Vasculitis
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Anne-Marie Lavigne; Valérie Gagnon Bruneau
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