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Öğe A Case of ANCA-Positive Vasculitis Without Lung Involvement: Eosinophilic Granulomatous Polyangiitis (EGPA)(Akdeniz Üniversitesi, 2025) Özdemir, Latif Emre; Göktürk, Laleş Yanık; Ayyıldız, OrhanABSTRACT Eosinophilic Granulomatous Polyangiitis (EGPA) is a vasculitic disease with multiple organ involvement, allergic rhinitis and asthma components. A 60-year-old male patient was admitted to our clinic with constitutional symptoms such as weakness and fatigue, persistent asthma and acute renal injury (ARI). He stated that he had widespread myalgia, night sweats, and occasional rashes on the body at the time of admission. A diagnosis of Eosinophilic Granulomatous Polyangiitis was made based on clinical and laboratory evaluations of the patient, who received multi-stage therapy for asthma and allergic rhinitis. We present this patient, who is quite rare, affects small and medium-sized vessels, and is among ANCA positive vasculitides such as Granulomatosis with Polyangiitis (GPA) and microscopic polyangiitis, to discuss with the literature.
