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Three cases of polymyositis/dermatomyositis complicated by pneumomediastinum
Keiko Shimamoto1, Yoshio Ozaki, Hideki Amuro
1First Department of Internal Medicine, Kansai Medical University.
Abstract:
Pneumomediastinum is a rare complication of dermatomyositis (DM) and Polymiositis (PM). We report here three cases of PM/DM who developed pneumomediastinum. First case was 61 years old woman with amyopathic dermatomyositis (aDM). Her aDM was complicated with skin ulceration due to vasculopathy, but complicated interstitial pneumonia was not severe. She developed subcutaneous emphysema and pneumomediastinum. Second case was 57 years old woman with DM, who had intractable skin phenomena and mild interstitial pneumonia. The patient became subcutaneous emphysema and pneumomediastinum following severe vasculopathy of skin. The last case was 63 years old man with PM. His PM was complicated with interstitial pneumonia. He had intractable respiratory symptom. Ten years later, he became subcutaneous emphysema and pneumomediastinum following pneumothorax. First and second cases suggest that their pneumomediastinum were due to vasculopathy. On the other hand, pneumomediastinum of the last patient seemed to be associated with interstitial pneumonia and steroid.
Insights
Pneumomediastinum is a rare complication in patients with dermatomyositis (DM) and polymyositis (PM). This study details three cases, highlighting potential links to vasculopathy and interstitial pneumonia in these inflammatory muscle diseases.
Area of Science:
- Rheumatology
- Pulmonology
- Dermatology
Background:
- Dermatomyositis (DM) and Polymyositis (PM) are idiopathic inflammatory myopathies.
- Pneumomediastinum is a rare but serious complication associated with these conditions.
- Understanding the specific mechanisms is crucial for patient management.
Observation:
- Three cases of pneumomediastinum in patients with DM/PM are presented.
- Case 1: A 61-year-old woman with amyopathic dermatomyositis (aDM) and skin vasculopathy developed subcutaneous emphysema and pneumomediastinum.
- Case 2: A 57-year-old woman with DM, skin phenomena, and mild interstitial pneumonia developed pneumomediastinum secondary to severe skin vasculopathy.
- Case 3: A 63-year-old man with PM and interstitial pneumonia developed pneumomediastinum following pneumothorax.
Findings:
- The first two cases suggest a strong association between pneumomediastinum and vasculopathy in DM.
- The third case indicates a potential link between pneumomediastinum, interstitial pneumonia, and corticosteroid treatment in PM.
- These findings underscore the diverse clinical manifestations and potential complications of DM and PM.
Implications:
- Early recognition of pneumomediastinum in DM/PM patients is vital for timely intervention.
- Further research is needed to elucidate the precise pathophysiology linking these conditions.
- This study contributes to the understanding of rare pulmonary complications in inflammatory myopathies.
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