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Pulmonary function tests, interstitial lung disease and lung function decline in outpatients with classic and clinically amyopathic dermatomyositis.

作者信息

George M D, Shah R, Kreider M, Miller W T, Merkel P A, Werth V P

机构信息

Division of Rheumatology, University of Pennsylvania, Philadelphia, PA, U.S.A.

Division of Pulmonary & Critical Care Medicine, University of Pennsylvania, Philadelphia, PA, U.S.A.

出版信息

Br J Dermatol. 2017 Jan;176(1):262-264. doi: 10.1111/bjd.14771. Epub 2016 Dec 7.

Abstract
摘要

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本文引用的文献

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Prognostic factors for myositis-associated interstitial lung disease.
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Pulmonary manifestations of polymyositis/dermatomyositis.
Semin Respir Crit Care Med. 2014 Apr;35(2):239-48. doi: 10.1055/s-0034-1371528. Epub 2014 Mar 25.
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An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management.
Am J Respir Crit Care Med. 2011 Mar 15;183(6):788-824. doi: 10.1164/rccm.2009-040GL.
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Interstitial lung disease in polymyositis and dermatomyositis.
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Interstitial lung disease in patients with polymyositis, dermatomyositis and amyopathic dermatomyositis.
Rheumatology (Oxford). 2005 Oct;44(10):1282-6. doi: 10.1093/rheumatology/keh723. Epub 2005 Jun 21.
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Dermatomyositis: an overview of recent progress with emphasis on dermatologic aspects.
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