Hou Ling, Zhao Jinbo, He Ting, Luo Yinhua, Su Ke, Li Yuanhong, Zhu Ruiyang
Central Hospital of Tujia and Miao Autonomous Prefecture, Hubei University of Medicine, Shiyan, People's Republic of China.
Cardiovascular Disease Center, Central Hospital of Tujia and Miao Autonomous Prefecture, Hubei University of Medicine, Enshi, Hubei Province, People's Republic of China.
J Inflamm Res. 2024 Aug 12;17:5285-5291. doi: 10.2147/JIR.S472889. eCollection 2024.
Granulomatosis with polyangiitis (GPA) is a necrotizing granulomatous vasculitis classified as an autoimmune small-vessel vasculitis. Clinically, approximately 80% of affected organs in GPA involve the upper/lower respiratory tract and kidneys, with cardiovascular system involvement being rare. Here, we report a case of a 50-year-old female patient who presented with sudden-onset chest pain lasting for 1 hour. The patient had normal body temperature, and markers of infection such as C-reactive protein and erythrocyte sedimentation rate were within normal limits. Electrocardiography revealed ST-segment elevation in inferior, precordial, and posterior leads. Emergency coronary angiography showed no significant obstructive disease, prompting consideration of vasospastic angina given the patient's recurrent chest pain symptoms and findings on laboratory and imaging studies. The patient underwent treatment including coronary vasospasm antagonists and immunomodulation, resulting in clinical improvement and subsequent discharge. During a 7-month follow-up period, the patient did not experience any further adverse cardiovascular events.
肉芽肿性多血管炎(GPA)是一种坏死性肉芽肿性血管炎,归类为自身免疫性小血管炎。临床上,GPA中约80%的受累器官累及上/下呼吸道和肾脏,心血管系统受累罕见。在此,我们报告一例50岁女性患者,该患者突发胸痛持续1小时。患者体温正常,C反应蛋白和红细胞沉降率等感染指标在正常范围内。心电图显示下壁、胸前导联和后壁导联ST段抬高。急诊冠状动脉造影未显示明显阻塞性病变,鉴于患者反复胸痛症状以及实验室和影像学检查结果,考虑为变异性心绞痛。该患者接受了包括冠状动脉痉挛拮抗剂和免疫调节在内的治疗,临床症状改善并随后出院。在7个月的随访期内,患者未发生任何进一步的不良心血管事件。