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Case Report

A case of anti-MDA5-positive rapidly progressive interstitial lung disease in a patient with clinically amyopathic dermatomyositis ameliorated by rituximab, in addition to standard immunosuppressive treatment

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Pages 536-540 | Received 18 Nov 2014, Accepted 29 Jan 2015, Published online: 12 Mar 2015
 

Abstract

Rapidly progressive interstitial lung disease (RP-ILD) in patients with clinically amyopathic dermatomyositis (CADM) associated with antibodies to melanoma differentiation-associated gene5 (MDA5) results in a high mortality rate.

We experienced a case of anti-MDA5-positive RP-ILD of CADM which showed a response to rituximab, although there was no significant effect due to standard immunosuppressive treatment. This case suggests that rituximab has the potential to offer an effective agent for the treatment of anti-MDA5-positive RP-ILD of CADM.

Acknowledgement

We thank Dr. Yoshinao Muro (Department of Dermatology, Nagoya University Graduate School of Medicine) for measuring the anti-MDA5 antibody level.

Conflict of interest

None.

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