Ryad Robert, Osman Alsayed, Almusa Ahmad, Gerges Peter, Sumbul-Yuksel Bahar
Internal Medicine, AdventHealth Orlando, Orlando, USA.
Internal Medicine, AdventHealth Orlando, Orlando , USA.
Cureus. 2023 Aug 29;15(8):e44324. doi: 10.7759/cureus.44324. eCollection 2023 Aug.
Dermatomyositis is a rare auto-immune inflammatory myopathy of unknown etiology. Several environmental factors, including vaccines, have been identified as potential triggers in genetically susceptible individuals. Since the beginning of the coronavirus disease 2019 (COVID-19) pandemic, the development of vaccines (mRNA and vector-based) has been the most effective tool in reducing the incidence, hospitalization rates, and mortality of COVID-19. However, among individuals with immune dysregulation and auto-immune conditions, unique challenges may arise with immune stimulation. We present a case of a dermatomyositis flare-up following severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination. A 40-year-old Hispanic female presented to the emergency department with shortness of breath, muscle pain and weakness, and skin rash for two days. She had been recently diagnosed with dermatomyositis six months prior based on clinical presentation, laboratory investigations, and characteristic muscle biopsy findings. She had been on treatment with mycophenolate mofetil, prednisone, and hydroxychloroquine since. She reported receiving the second dose of the BNT162b2 COVID-19 vaccine one day prior to the onset of symptoms. Physical examination revealed erythematous plaques over her cheeks, upper chest, and arms, in addition to Gottron papules on her hands. She had reduced proximal muscle strength and scattered dry crackles bilaterally on lung auscultation. Her laboratory investigations were remarkable for elevated erythrocyte sedimentation rate, C-reactive peptide, creatinine kinase, and troponin T. The SARS- CoV-2 PCR test was negative. CT scan of the chest showed evidence of pneumonitis. A diagnosis of the dermatomyositis flare-up potentially secondary to the SARS-CoV-2 BNT162b2 vaccine was established. The patient was admitted and treated with pulse steroids and intravenous immunoglobulin. She responded well to therapy and was discharged home four days later. There have been several reports of a new onset of dermatomyositis following the SARS-CoV-2 vaccine which highlights the need for further large-scale studies to estimate the prevalence of such adverse effects. The benefits of the SARS-CoV-2 vaccine outweigh the risks even among patients with auto-immune and rheumatologic conditions; however, it is important for clinicians to recognize the possibility of occurrence of such events in order to manage patients appropriately.
皮肌炎是一种病因不明的罕见自身免疫性炎性肌病。包括疫苗在内的多种环境因素已被确定为基因易感性个体的潜在触发因素。自2019冠状病毒病(COVID-19)大流行开始以来,疫苗(信使核糖核酸疫苗和载体疫苗)的研发一直是降低COVID-19发病率、住院率和死亡率的最有效工具。然而,在免疫调节异常和自身免疫性疾病患者中,免疫刺激可能会带来独特的挑战。我们报告一例严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗接种后皮肌炎发作的病例。一名40岁的西班牙裔女性因呼吸急促、肌肉疼痛和无力以及皮疹两天前来急诊科就诊。她六个月前根据临床表现、实验室检查和典型的肌肉活检结果被诊断为皮肌炎。自那以后,她一直在接受霉酚酸酯、泼尼松和羟氯喹治疗。她报告在症状出现前一天接种了第二剂BNT162b2 COVID-19疫苗。体格检查发现她的脸颊、上胸部和手臂有红斑性斑块,手部有Gottron丘疹。她近端肌肉力量减弱,肺部听诊双侧有散在的干性啰音。她的实验室检查结果显示红细胞沉降率、C反应蛋白、肌酸激酶和肌钙蛋白T升高。SARS-CoV-2聚合酶链反应检测呈阴性。胸部CT扫描显示有肺炎迹象。确诊为可能继发于SARS-CoV-2 BNT162b2疫苗的皮肌炎发作。患者入院后接受了脉冲类固醇和静脉注射免疫球蛋白治疗。她对治疗反应良好,四天后出院回家。已有数篇关于SARS-CoV-2疫苗接种后新发皮肌炎的报道,这凸显了进一步进行大规模研究以评估此类不良反应发生率的必要性。即使在患有自身免疫性和风湿性疾病的患者中,SARS-CoV-2疫苗的益处也大于风险;然而,临床医生认识到发生此类事件的可能性以便对患者进行适当管理非常重要。