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An Autopsy Case of Anti-melanoma Differentiation-associated Gene-5 Antibody-positive Clinical Amyopathic Dermatomyositis Complicated by Rapidly Progressive Interstitial Lung Disease

机译:抗黑素瘤分化相关基因5抗体阳性的肌病性皮肌炎合并快速进展性间质性肺病的尸检病例

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A 62-year-old man presented with heliotrope rash, Gottron's sign, and mild muscle weakness. Both of his lung fields showed interstitial changes that worsened rapidly. He was diagnosed with clinical amyopathic dermatomyositis with rapidly progressive interstitial lung disease. The patient died of respiratory failure, despite the administration of immunosuppressive therapy. Autopsy revealed diffuse alveolar damage. An antibody analysis, which was performed postmortem, detected the presence of anti-melanoma differentiation-associated gene (MDA)-5 antibodies. Clinicians should note the clinical, radiologic, and serologic findings to predict anti-MDA-5 antibody-associated rapidly progressive interstitial lung disease.
机译:一名62岁的男子出现了天芥菜皮疹,Gottron的体征和轻度的肌肉无力。他的两个肺野都显示出组织间变化,并迅速恶化。他被诊断出患有快速进展性间质性肺疾病的临床肌病性皮肌炎。尽管进行了免疫抑制治疗,该患者仍死于呼吸衰竭。尸检显示弥漫性肺泡损伤。死后进行的抗体分析检测到抗黑素瘤分化相关基因(MDA)-5抗体的存在。临床医生应注意临床,放射学和血清学检查结果,以预测抗MDA-5抗体相关的快速进行性间质性肺疾病。

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