Dermatomyositis is an autoimmune disease that is considered a subset of idiopathic inflammatory myopathy. It is characterized by a skin rash with progressive muscle weakness. Pneumomediastinum is a rapidly progressive complication of dermatomyositis, which is hypothesized to be a result of ruptured subpleural cysts, pulmonary vasculopathy, and steroid-mediated weakening of alveolar walls. This complication is associated with a high mortality rate of 30%. Hence, it should be rapidly investigated and treated when there is a high clinical suspicion. In this article, we report a rare case of patient with dermatomyositis (DM) who developed pneumomediastinum and discussed a literature review of this occurrence.
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Lee et al. (2021) studied this question.
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