Spontaneous pneumomediastinum: An extra muscular manifestation of anti-MDA5 dermatomyositis. Report of 2 cases

Pablo Arango Guerra , Santiago Monsalve Yepes , Andrés Chavarriaga Restrepo , Carlos Jaime Velasquez Franco
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Abstract

The use of specific antibodies in inflammatory myopathies has improved the characterization of this disease, identifying different clinical phenotypes. Patients with dermatomyositis (DM) and anti-MDA5 antibodies display typical skin symptoms, lesser muscular involvement, and a prevalence of interstitial lung disease (ILD) of up to 91%. Beyond ILD, spontaneous pneumomediastinum (SN) has been identified as a rare but potentially fatal pulmonary manifestation. Two cases of this complication in patients with anti-MDA5 DM are reported.

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自发性气胸:抗MDA5皮肌炎的一种肌肉外表现。两个病例的报告
在炎症性肌病中使用特异性抗体改善了这种疾病的特征描述,确定了不同的临床表型。皮肌炎(DM)和抗MDA5抗体患者表现出典型的皮肤症状,肌肉受累较轻,间质性肺病(ILD)发病率高达91%。除间质性肺病外,自发性气胸(SN)也是一种罕见但可能致命的肺部表现。抗 MDA5 DM 患者中出现这种并发症的病例有两例。
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