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Successful rituximab treatment for severe rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive juvenile dermatomyositis: a case report and literature review.

Kentaro NishiMasao OguraNaotaka TamaiMasafumi GimaKentaro IdeGoro KoinumaKoichi KameiShuichi Ito
Published in: Pediatric rheumatology online journal (2022)
Our literature review suggest that JDM with RP-ILD has a high mortality rate. In JDM, rituximab may be a promising treatment option for RP-ILD. In the future, the efficacy of rituximab in the early phases of ILD should be investigated.
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