首页> 外文期刊>Journal Of Cutaneous Immunology and Allergy >A case of anti‐OJ antibody‐positive polymyositis with marked muscle involvement and interstitial lung disease
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A case of anti‐OJ antibody‐positive polymyositis with marked muscle involvement and interstitial lung disease

机译:一种抗OJ抗体阳性多发性肌炎,具有标记的肌肉受累和间质性肺病

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An 83‐year‐old man with muscle involvement and interstitial lung disease (ILD) was diagnosed with anti‐OJ antibody (Ab)‐positive polymyositis (PM). He did not have Raynaud's phenomenon, heliotrope rash, Gottron's sign, fever, arthralgia, or mechanic's hand. A literature review of 21 anti‐OJ Ab‐positive patients described that the diagnoses were as follows: 10 with PM, five with dermatomyositis, five with ILD, and 1 with overlap syndrome of PM and rheumatoid arthritis. Myositis was observed in 16, ILD in 19, and skin rash in 5. Physicians need to be aware of the existence of patients with anti‐OJ Ab who have myositis and ILD.
机译:患有抗OJ抗体(AB) - 阳性多发性肌炎(PM)诊断出一个83岁的男性患有肌肉参与和间质肺病(ILD)。 他没有Raynaud的现象,Heliotrope皮疹,Gottron的标志,发烧,关节痛或机械师的手。 对21例抗OJ AB阳性患者的文献综述描述了诊断如下:10含有PM,5例,带有皮肤病,五种,具有ILD的5个,1μm和下颌综合征和类风湿性关节炎。 肌炎在19岁,ILD IND中观察到,并且皮疹5.医生需要意识到患有肌炎和ILD的抗OJ AB患者的存在。

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