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11. An unusual case of dermatomyositis with anti-small ubiquitin-like modifier activating enzyme (SAE) antibodies present

机译:11.皮肌平滑肌炎的罕见病例出现了抗小泛素样修饰物激活酶(SAE)抗体

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摘要

IntroductionIdiopathic inflammatory myopathies (IIM) have long been diagnosed using a defined number of clinical criteria (Bohan and Peter). The emergence of new myositis specific antibodies (MSAs) and their relation to specific disease phenotypes may be useful in establishing a new clinical-serological diagnostic criteria for different disease presentations and thus help to determine management and prognosis. We present a case of dermatomyositis (DM) where limb subcutaneous oedema; a rare manifestation of the disease, and severe dysphagia were prominent clinical features in addition with the presence of anti-small ubiquitin-like modifier activating enzyme (SAE) antibodies.
机译:简介长期以来,已使用一定数量的临床标准(Bohan和Peter)诊断出特发性炎症性肌病(IIM)。新的肌炎特异性抗体(MSA)的出现及其与特定疾病表型的关系可能有助于建立针对不同疾病表现的新临床血清学诊断标准,从而有助于确定治疗和预后。我们提出了一例皮肌炎(DM),其中肢体皮下有水肿。罕见的疾病表现,严重的吞咽困难是除抗小泛素样修饰物激活酶(SAE)抗体外的重要临床特征。

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