Aljaber Latifa, Schutz Peter, Ennis Daniel, Jack Kristin, Huang Kun
Internal Medicine, University of British Columbia, Faculty of Medicine, Vancouver, CAN.
Pathology, University of British Columbia, Faculty of Medicine, Vancouver, CAN.
Cureus. 2024 Dec 28;16(12):e76540. doi: 10.7759/cureus.76540. eCollection 2024 Dec.
Idiopathic inflammatory myopathies (IIM), or myositis, are a heterogeneous group of autoimmune disorders that can affect multiple organs, including the muscles, skin, joints, lungs, heart, and gastrointestinal tract. While new-onset myositis has been reported following SARS-CoV-2 infection, cases associated with COVID-19 vaccination remain rare. We describe a unique case of severe progressive edematous facial myositis resembling angioedema in a 22-year-old man, with onset one to two weeks after receiving dual SARS-CoV-2 and influenza vaccinations. This ultimately led to a diagnosis of systemic inflammatory myositis with extensive involvement of proximal muscles in the arms and legs. We outline the clinical course, diagnostic investigations, and treatments, and discuss the potential molecular mechanisms and existing literature on inflammatory myositis induced by SARS-CoV-2 infection or mRNA-based vaccination.
特发性炎性肌病(IIM),即肌炎,是一组异质性自身免疫性疾病,可累及多个器官,包括肌肉、皮肤、关节、肺、心脏和胃肠道。虽然已有报告称新型冠状病毒2(SARS-CoV-2)感染后会新发肌炎,但与新型冠状病毒病(COVID-19)疫苗接种相关的病例仍然罕见。我们描述了一例独特的病例,一名22岁男性出现严重进行性水肿性面部肌炎,类似血管性水肿,在接种SARS-CoV-2和流感疫苗后一至两周发病。这最终导致诊断为全身性炎性肌病,上肢和下肢近端肌肉广泛受累。我们概述了临床过程、诊断检查和治疗方法,并讨论了SARS-CoV-2感染或基于信使核糖核酸(mRNA)的疫苗接种诱发炎性肌病的潜在分子机制及现有文献。