Park Sung Hwan, Kum Yoon-Seup, Kim Kyung-Chan, Choe Jung-Yoon, Park Sung-Hoon, Kim Seong-Kyu
Department of General Surgery, Catholic University of Daegu School of Medicine, Daegu, South Korea.
Rheumatol Int. 2009 Aug;29(10):1231-5. doi: 10.1007/s00296-008-0808-0. Epub 2008 Dec 18.
Amyopathic dermatomyositis (ADM) is recognized as a variant phenotype of dermatomyositis and characterized by typical skin manifestations without evidence of muscular inflammation. While interstitial lung disease (ILD) is occasionally found as one of the lung manifestations in ADM patients, the development of a pneumomediastinum and/or subcutaneous emphysema in this disease entity is one of the extremely rare pulmonary complications. These latter complicated pulmonary manifestations have been usually reported in idiopathic ADM with ILD without any other associated medical conditions. We report a case presented with the spontaneous pneumomediastinum and subcutaneous emphysema in both ADM and cryptogenic organizing pneumonia during adjuvant chemotherapy based on cyclophosphamide for breast cancer.
无肌病性皮肌炎(ADM)被认为是皮肌炎的一种变异型,其特征为有典型的皮肤表现但无肌肉炎症证据。虽然间质性肺病(ILD)偶尔在ADM患者中作为肺部表现之一被发现,但在该疾病实体中出现纵隔气肿和/或皮下气肿是极为罕见的肺部并发症之一。这些后者复杂的肺部表现通常在伴有ILD且无任何其他相关内科疾病的特发性ADM中报道。我们报告一例在基于环磷酰胺的辅助化疗治疗乳腺癌期间,同时患有ADM和隐源性机化性肺炎并出现自发性纵隔气肿和皮下气肿的病例。