Rapidly Progressive Interstitial Lung Disease Originating from Clinically Amyopathic Dermatomyositis Associated with Positive Anti-MDA 5 Antibody: a Case Report and Literature Review-Reference-Cited by-同舟云学术

Rapidly Progressive Interstitial Lung Disease Originating from Clinically Amyopathic Dermatomyositis Associated with Positive Anti-MDA 5 Antibody: a Case Report and Literature Review

Published:2019-09-02 Issue:11 Volume:1 Page:915-920
ISSN:2523-8973
Container-title:SN Comprehensive Clinical Medicine
language:en
Short-container-title:SN Compr. Clin. Med.

Author:

Huang Yanhua^ORCID,Mao Minhua

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/content/pdf/10.1007/s42399-019-00127-9.pdf

Reference31 articles.

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2. Mammen AL. Dermatomyositis and polymyositis. Ann N Y Acad Sci. 2010;1184(1):134–53.

3. Cao H, Xia Q, Pan M, Zhao X, Li X, Shi R, et al. Gottron papules and Gottron sign with ulceration: a distinctive cutaneous feature in a subset of patients with classic dermatomyositis and clinically amyopathic dermatomyositis. J Rheumatol. 2016;43(9):1735–42.

4. Mukae H, Ishimoto H, Sakamoto N, Hara S, Kakugawa T, Nakayama S, et al. Clinical differences between interstitial lung disease associated with clinically amyopathic dermatomyositis and classic dermatomyositis. Chest. 2009;136(5):1341–7.

5. González-Moreno J, Raya-Cruz M, Losada-Lopez I, et al. Rapidly progressive interstitial lung disease due to anti-MDA5 antibodies without skin involvement: a case report and literature review. Rheumatol Int. 2018:1–4.

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