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作 者:陈文文 夏育民[1] CHEN Wenwen;XIA Yumin(Department of Dermatology,the Second Affiliated Hospital,Xi'an Jiaotong University,Xi'an 710004,China)
机构地区:[1]西安交通大学第二附属医院皮肤科,陕西西安710004
出 处:《中国皮肤性病学杂志》2021年第1期83-86,共4页The Chinese Journal of Dermatovenereology
摘 要:患者女,31岁,多发肌肉疼痛4个月,咳嗽、气短2个月,发热3 d。肌电图提示肌炎活动期;特发性炎性肌炎谱示:抗MDA5抗体IgG(3+),抗Ro-52抗体IgG(3+);胸部CT提示两肺间质性改变及感染。诊断:皮肌炎,肺间质病变,Ⅰ型呼吸衰竭,肺部感染。A 31-year-old female presented multiple muscle pain for four months,cough and shortness of breath for two months,and fever for three days.Electromyogram indicated the active phase of myositis.Idiopathic inflammatory myositis spectrum:anti-MDA5 antibody IgG(3+),anti-Ro-52 antibody IgG(3+).CT scan of the lung revealed pulmonary interstitial change and infection.The diagnosis was dermatomyositis,interstitial lung disease,typeⅠrespiratory failure,pulmonary infection.
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