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抗 MDA-5 抗体相关性皮肌炎的治疗性血浆置换治疗作用:病例报告及文献复习

The role of therapeutic plasma exchange in clinically amyopathic dermatomyositis with MDA-5 antibody: A case report and review of the literature.

机构信息

Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, USA.

出版信息

J Clin Apher. 2020 Sep;35(5):483-487. doi: 10.1002/jca.21815. Epub 2020 Jul 18.

Abstract

Clinically amyopathic dermatomyositis (CADM) is a rare, aggressive variant of dermatomyositis associated with interstitial lung disease (ILD) and refractoriness to immunosuppressants. Antibodies against melanoma differentiation-associated gene 5 (MDA-5) are often found in patients with CADM. We report a patient with advanced CADM with ILD and MDA-5 antibodies who failed to improve with immunosuppressants. We performed 2 TPE over 3 days, using 5% albumin as replacement fluid. Although five total TPE were planned, he was transferred for lung transplant evaluation after the second TPE; he died 16 days after transfer without receiving a transplant. A literature review identified four patients with CADM and MDA-5 antibodies treated with TPE; all experienced symptomatic improvement of their ILD. We attribute our patient's outcome to the advanced nature of his disease rather than a failure of TPE. Additional research may indicate a possible reclassification of CADM with MDA-5 antibodies in future ASFA guidelines.

摘要

临床无肌病性皮肌炎(CADM)是一种罕见且侵袭性较强的皮肌炎变异型,与间质性肺病(ILD)和免疫抑制剂抵抗有关。抗黑色素瘤分化相关基因 5(MDA-5)抗体常存在于 CADM 患者中。我们报告了一例患有进展性 CADM 和ILD 以及 MDA-5 抗体的患者,他对免疫抑制剂治疗没有改善。我们在 3 天内进行了 2 次 TPE,使用 5%白蛋白作为替代液。尽管计划进行 5 次 TPE,但在第二次 TPE 后他被转往进行肺移植评估;他在转院后 16 天死亡,没有接受移植。文献回顾发现有 4 例 CADM 合并 MDA-5 抗体的患者接受了 TPE 治疗;所有患者的ILD 症状均有改善。我们认为患者的预后是由于疾病的晚期性质,而不是 TPE 的失败。进一步的研究可能表明在未来的 ASFA 指南中,对 MDA-5 抗体相关的 CADM 进行重新分类。

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