1例哮喘样表现的嗜酸性肉芽肿性多血管炎患者的临床分析

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中图分类号：R593.2 文献标志码：A

Abstract： This study summarized the diagnosis and treatment of a patient with eosinophilic granulomatosis with polyangitis（EGPA），primarily manifesting as allergic asthma，admitted to the People's Hospital of Shaodong in October 2O24.Based on clinical symptomsand diagnostic findings，the patient was definitively diagnosedwith EGPA.Treatment included oral methylprednisolone foranti-inflammatory therapy and subcutaneous mepolizumab injections.After one month of therapy，the patient'sasthma-like symptoms significantly improved.At the two-month follow-up，thepatient remained stable with sustained clinical resolution.

Key words： allergic asthma;eosinophilic granulomatosis with polyangiitis；eosinophil

嗜酸性肉芽肿性多血管炎（eosinophilic granulomatosis with polyangitis，EGPA）是一种罕见的自身免疫性疾病，主要表现为嗜酸性粒细胞（eosinophilic，EOS）增多、浸润及中小血管坏死性肉芽肿性炎症[1-2]。（剩余6211字）