Mueller Sandro Manuel, Schaefer Jacques Emanuel, Hortobagyi Tibor, Thurnheer Robert
Internal Medicine, Kantonsspital Münsterlingen, Münsterlingen, TG, Switzerland
Kantonsspital Münsterlingen, Münsterlingen, TG, Switzerland.
BMJ Case Rep. 2025 May 5;18(5):e263689. doi: 10.1136/bcr-2024-263689.
Idiopathic inflammatory myopathies (IIM) represent a diverse group of systemic autoimmune disorders characterised by skeletal muscle weakness with variable clinical manifestations.Dermatomyositis (DM) is a heterogeneous IIM and is associated with progressive muscle weakness, with characteristic skin features, and with an increased risk of malignancy. Here, we report a previously healthy man in his early 40s who presented to the emergency department with a 14-day history of symmetric progressive proximal muscle weakness. Both upper arms were painful and swollen, and they displayed marked weakness in arm elevation. Climbing stairs was no longer possible due to muscle weakness and pain. A facial and truncal rash as well as periungual erythema were noted. Laboratory analysis revealed highly elevated creatine kinase. Based on these findings, the diagnosis of DM was confirmed. A comprehensive search for malignancy revealed a non-palpable pure seminoma. While DM as a paraneoplastic phenomenon of seminoma is extremely rare, our case underlines the importance of a thorough tumour search.
特发性炎性肌病(IIM)是一组多样的系统性自身免疫性疾病,其特征为骨骼肌无力,临床表现各异。皮肌炎(DM)是一种异质性IIM,与进行性肌无力、特征性皮肤表现以及恶性肿瘤风险增加有关。在此,我们报告一名40岁出头的既往健康男性,他因对称进行性近端肌无力14天就诊于急诊科。双臂疼痛肿胀,抬臂时明显无力。由于肌肉无力和疼痛,已无法爬楼梯。发现有面部和躯干皮疹以及甲周红斑。实验室分析显示肌酸激酶高度升高。基于这些发现,确诊为DM。全面的恶性肿瘤筛查发现了一个触诊不到的纯精原细胞瘤。虽然DM作为精原细胞瘤的副肿瘤现象极为罕见,但我们的病例强调了彻底肿瘤筛查的重要性。