An autopsy case of anti-melanoma differentiation-associated gene-5 antibody-positive clinical amyopathic dermatomyositis complicated by rapidly progressive interstitial lung disease

8Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

Abstract

A 62-year-old man presented with heliotrope rash, Gottron’s sign, and mild muscle weakness. Both of his lung fields showed interstitial changes that worsened rapidly. He was diagnosed with clinical amyopathic dermatomyositis with rapidly progressive interstitial lung disease. The patient died of respiratory failure, despite the administration of immunosuppressive therapy. Autopsy revealed diffuse alveolar damage. An antibody analysis, which was performed postmortem, detected the presence of anti-melanoma differentiation-associated gene (MDA)-5 antibodies. Clinicians should note the clinical, radiologic, and serologic findings to predict anti-MDA-5 antibody-associated rapidly progressive interstitial lung disease.

Cite

CITATION STYLE

APA

Yoshida, N., Kaieda, S., Tomozoe, K., Tajiri, M., Wakasugi, D., Okamoto, M., … Hoshino, T. (2016). An autopsy case of anti-melanoma differentiation-associated gene-5 antibody-positive clinical amyopathic dermatomyositis complicated by rapidly progressive interstitial lung disease. Internal Medicine, 55(12), 1653–1659. https://doi.org/10.2169/internalmedicine.55.6055

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free