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Published in: Modern Rheumatology 4/2012

01-08-2012 | Case Report

Amyopathic dermatomyositis developing rapidly progressive interstitial lung disease with elevation of anti-CADM-140/MDA5 autoantibodies

Authors: Shinji Sato, Masataka Kuwana, Takashi Fujita, Yasuo Suzuki

Published in: Modern Rheumatology | Issue 4/2012

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Abstract

Anti-clinically amyopathic dermatomyositis (CADM)-140/MDA5 autoantibodies are specifically detected in patients with dermatomyositis and are known to have a strong association with rapidly progressive interstitial lung disease (RP-ILD). Here we report an amyopathic dermatomyositis (ADM) patient who developed RP-ILD characterized by elevated anti-CADM-140/MDA5 titer. Respiratory symptoms gradually improved, and anti-CADM-140/MDA5 titer decreased in parallel to below the cutoff level. It may be useful to quantify CADM-140-specific autoantibodies for monitoring disease activity in patients with ADM and RP-ILD.
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Metadata
Title
Amyopathic dermatomyositis developing rapidly progressive interstitial lung disease with elevation of anti-CADM-140/MDA5 autoantibodies
Authors
Shinji Sato
Masataka Kuwana
Takashi Fujita
Yasuo Suzuki
Publication date
01-08-2012
Publisher
Springer Japan
Published in
Modern Rheumatology / Issue 4/2012
Print ISSN: 1439-7595
Electronic ISSN: 1439-7609
DOI
https://doi.org/10.1007/s10165-011-0558-9

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