Kimura Disease With Eosinophilic Granulomatosis With Polyangiitis Successfully Treated by Mepolizumab

木村病伴嗜酸性肉芽肿性血管炎经美泊利单抗成功治疗

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Abstract

Diagnosis of Kimura's disease should be considered if a middle-aged Asian male patient presents with painless enlargement of cervical lymph nodes, eosinophilia, and elevated serum total IgE level. Patients with Kimura's disease can have concurrent EGPA or presentations consistent with EGPA. IL-5 antibody treatment can be considered for these patients.

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