静脉注射免疫球蛋白(IVIG)治疗多发性肌炎相关急性间质性肺疾病的显著疗效

IF 1.8 Q3 RESPIRATORY SYSTEM

European Clinical Respiratory Journal Pub Date : 2020-10-26 DOI:10.1080/20018525.2020.1840706

Soran Peshbahar, Elisabeth Bendstrup

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引用次数: 5

摘要

多发性肌炎(PM)和皮肌炎(DM)是自身免疫性炎症性肌病的亚型。间质性肺疾病(ILD)累及在PM/DM中很常见。在DM/PM-ILD中没有免疫抑制的证据基础，目前的证据是基于病例和专家意见。我们报告一位63岁男性，因PM-ILD而导致严重呼吸衰竭，经静脉注射免疫球蛋白治疗成功，急性期恢复，存活超过4年。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Remarkable benefits of intravenous immunoglobulin (IVIG) in a patient with polymyositis-associated acute interstitial lung disease.

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Remarkable benefits of intravenous immunoglobulin (IVIG) in a patient with polymyositis-associated acute interstitial lung disease.

Polymyositis (PM) and dermatomyositis (DM) are subtypes of autoimmune inflammatory myopathies. Interstitial lung disease (ILD) involvement is common in PM/DM. There is no evidence base for immunosuppression in DM/PM-ILD and current evidence is based on case stories and expert opinions. We present a 63-year-old male with severe respiratory failure due to PM-ILD who was treated successfully with intravenous immunoglobulin, recovered the acute phase and survived more than 4 years.

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来源期刊

European Clinical Respiratory Journal RESPIRATORY SYSTEM-

CiteScore

3.80

自引率

0.00%

发文量

审稿时长

16 weeks