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急性呼吸窘迫综合征在10个月后复发，最初表现为多发性肌炎。

Acute respiratory distress syndrome relapsing in 10 months with an initial manifestation of polymyositis.

作者信息

Takeda Yukihisa, Ono Mariko, Kinoshita Hayato, Nagatomo Yoko, Miyauchi Hiroki, Tsukamoto Hiroshi, Nakamura Hiroyuki, Aoshiba Kazutetsu

机构信息

Department of Respiratory Medicine Tokyo Medical University Ibaraki Medical Center Ibaraki Japan.

Department of Respiratory Medicine Tokyo Medical University Tokyo Japan.

出版信息

Clin Case Rep. 2021 Dec 6;9(12):e05147. doi: 10.1002/ccr3.5147. eCollection 2021 Dec.

DOI:10.1002/ccr3.5147
PMID:34925833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8647200/
Abstract

Autoimmune disorders are an important cause of acute respiratory distress syndrome (ARDS). We report a case of a patient with steroid-responsive ARDS that relapsed in 10 months with an initial manifestation of seronegative polymyositis. ARDS associated with polymyositis may develop earlier than myopathy and may relapse later.

摘要

自身免疫性疾病是急性呼吸窘迫综合征（ARDS）的一个重要病因。我们报告一例对类固醇有反应的ARDS患者，该患者在10个月后复发，最初表现为血清阴性多发性肌炎。与多发性肌炎相关的ARDS可能比肌病更早出现，且可能在后期复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a796/8647200/adefdab9ccbe/CCR3-9-e05147-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a796/8647200/4bb947671e6c/CCR3-9-e05147-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a796/8647200/adefdab9ccbe/CCR3-9-e05147-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a796/8647200/4bb947671e6c/CCR3-9-e05147-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a796/8647200/adefdab9ccbe/CCR3-9-e05147-g003.jpg

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Interstitial Lung Disease in Polymyositis and Dermatomyositis.多发性肌炎和皮肌炎中的间质性肺疾病。
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