首页> 美国卫生研究院文献>BMJ Case Reports >Case Report: Polyangiitis overlap syndrome of granulomatosis with polyangiitis (Wegener's granulomatosis) and eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome)
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Case Report: Polyangiitis overlap syndrome of granulomatosis with polyangiitis (Wegener's granulomatosis) and eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome)

机译:病例报告:肉芽肿合并多血管炎(韦格纳肉芽肿)和嗜酸性肉芽肿合并多血管炎(Churg-Strauss综合征)的多血管炎重叠综合征

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摘要

Polyangiitis overlap syndrome is defined as systemic vasculitis that cannot be classified into one of the well-defined vasculitic syndromes. In this report, a female patient who presented with vasculitis-like and asthmatic symptoms was diagnosed as having polyangiitis overlap syndrome of granulomatosis with polyangiitis (GPA; formerly known as Wegener's granulomatosis) and eosinophilic granulomatosis with polyangiitis (EGPA; formerly known as Churg-Strauss syndrome). The patient fulfilled the American College of Rheumatology diagnostic criteria for GPA and EGPA. She was successfully treated with immunosuppressants and steroids and has been in remission for 20 months. It is important to establish a proper diagnosis and introduce an appropriate treatment modality in patients with this rare and serious pathology to prevent irreversible organ damage.
机译:多血管炎重叠综合征定义为系统性血管炎,不能归类为定义明确的血管综合征之一。在该报告中,一名女性患者出现血管样炎和哮喘症状,被诊断为肉芽肿合并多血管炎(GPA;以前称为韦格纳肉芽肿)和嗜酸性肉芽肿合并多血管炎(EGPA;以前称为Churg-Strausss)的多血管炎重叠综合征。综合症)。该患者符合美国风湿病学会对GPA和EGPA的诊断标准。她已成功接受免疫抑制剂和类固醇治疗,已缓解20个月。重要的是要为患有这种罕见和严重病理的患者建立适当的诊断并引入适当的治疗方式,以防止不可逆的器官损害。

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