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肉芽肿性多血管炎误诊为肺曲霉病1例
http://www.100md.com 2019年9月9日 中国医药导报 2019年第18期
     付晓桐 姜春阳 李玲

    [摘要] 肉芽肿性多血管炎是一种自身免疫性疾病,其临床表现多种多样,容易与侵袭性肺曲霉病相混淆。本文报道了1例44岁中年男性肉芽肿性多血管炎误诊为侵袭性肺曲霉病的病例,通過讨论对两者的鉴别诊断,提高了临床医生对肉芽肿性多血管炎的诊断及鉴别诊断的能力。

    [关键词] 肉芽肿性多血管炎;自身免疫性疾病;侵袭性肺曲霉病;误诊;鉴别诊断

    [中图分类号] R563 ? ? ? ? ?[文献标识码] A ? ? ? ? ?[文章编号] 1673-7210(2019)06(c)-0144-04

    A case of granulomatosis with polyangiitis misdiagnosed as invasive pulmonary asperillosis

    FU Xiaotong ? JIANG Chunyang ? LI Ling

    Graduate School, Tianjin University of Traditional Chinese Medicine, Tianjin ? 300193, China

    [Abstract] Granulomatosis with polyangiitis (GPA) is an autoimmune disease with a variety of clinical manifestations that are easily confused with invasive pulmonary asperillosis (IPA). This article reports a case of a 44-year-old man with GPA misdiagnosed as IPA. Through the discussion of the differential diagnosis of the two diseases, the ability of clinician′s diagnosis and differential diagnosis in GPA was improved.

    [Key words] Granulomatosis with polyangiitis; Autoimmune diseases; Invasive pulmonary asperillosis; Misdiagnose; Differential diagnosis ......

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