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Anti-glycyl tRNA synthetase antibody associated interstitial lung disease without symptoms of polymyositis/dermatomyositis

机译:抗甘氨酰tRNa合成酶抗体相关的间质性肺病没有多发性肌炎/皮肌炎的症状

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摘要

Anti-Glycyl tRNA synthetase (EJ) autoantibody is a form of eight anti-aminoacyl tRNA synthetase (ARS) antibodies which frequently associate with polymyositis (PM) and dermatomyositis (DM). Interstitial lung disease (ILD) rarely is an only disease among those patients in which patients with anti-EJ antibody are fairly common, however, their pathological features have never been described. Here, we report a case of anti-EJ antibody associated ILD without symptoms of PM/DM. A 56 year-old woman presented rapidly progressing dyspnea. Her radiograph showed ILD and wedge lung biopsy was taken for pathological diagnosis. The biopsy showed cellular and fibrotic ILD best fitting to non-specific interstitial pneumonia along with the features of acute lung injury. The patient was treated with high dose methylprednisolone followed by combination of prednisolone and cyclosporine, which showed good response.
机译:抗糖基tRNA合成酶(EJ)自身抗体是八种抗氨酰基tRNA合成酶(ARS)抗体的一种形式,通常与多发性肌炎(PM)和皮肌炎(DM)相关。间质性肺疾病(ILD)很少是那些抗EJ抗体相当普遍的患者中的唯一疾病,但是,其病理特征从未被描述过。在这里,我们报告一例与EJ抗体相关的ILD抗体,无PM / DM症状。一名56岁的妇女表现出快速发展的呼吸困难。她的X光片显示ILD和楔形肺活检用于病理诊断。活检显示,细胞和纤维化ILD最适合非特异性间质性肺炎,并具有急性肺损伤的特征。患者接受高剂量甲基强的松龙治疗,然后联合泼尼松龙和环孢霉素治疗,均显示良好的反应。

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