Department of Cardiovascular Medicine, Chiba University Graduate School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Department of Allergy and Clinical Immunology, Chiba University Hospital, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8677, Japan.
Clin Rheumatol. 2023 Sep;42(9):2507-2514. doi: 10.1007/s10067-023-06648-y. Epub 2023 Jun 1.
Myocarditis has been reported as a life-threatening complication of adult-onset Still's disease (AOSD), but fulminant myocarditis with AOSD is very rare. We hereby report a case of a 43-year-old female with fulminant myocarditis with AOSD. She had a refractory AOSD and cardiogenic shock with markedly elevated ferritin level up to 67,370 ng/mL. She was successfully treated with canakinumab and mechanical circulatory support (MCS) such as venoarterial extracorporeal membrane oxygenation and Impella CP. We also reviewed the previous cases of fulminant myocarditis with AOSD published from 1976 to December 2022, and only 8 cases of fulminant myocarditis with AOSD have been reported. The characteristics of these cases showed that the average age at presentation was 37.6 years (range 24-47 years). The time to myocarditis from the onset of AOSD ranged from 2 weeks to 2 years; however, most cases developed myocarditis within 1 year. Initial presenting symptoms included fever, dyspnea, chest pain, myalgia, rash, and sore throat. The median peak ferritin was 13,000 ng/mL. Left ventricular ejection fractions were not greater than 35%. Our case was the first reported case successfully treated with canakinumab and MCS. This review suggests that myocarditis may be an early phase of the complication in patients with AOSD, and the severity of AOSD may correlate with the severity of myocarditis. Canakinumab for AOSD and MCS for fulminant myocarditis may be one of the choices for overcoming the comorbidities.
成人斯蒂尔病(AOSD)可引起致命性心肌炎并发症,但 AOSD 合并暴发性心肌炎非常罕见。我们在此报告一例 AOSD 合并暴发性心肌炎患者。该患者为 43 岁女性,患有难治性 AOSD 和心源性休克,铁蛋白水平显著升高至 67370ng/ml。经卡那单抗和机械循环支持(MCS)如静脉动脉体外膜肺氧合和 Impella CP 治疗后痊愈。我们还回顾了 1976 年至 2022 年 12 月期间发表的 AOSD 合并暴发性心肌炎的既往病例,仅报告了 8 例 AOSD 合并暴发性心肌炎。这些病例的特征表明,发病时的平均年龄为 37.6 岁(范围 24-47 岁)。从 AOSD 发病到心肌炎的时间为 2 周至 2 年,但大多数病例在 1 年内发生心肌炎。首发症状包括发热、呼吸困难、胸痛、肌痛、皮疹和咽痛。中位铁蛋白峰值为 13000ng/ml。左心室射血分数均不大于 35%。我们的病例是首例成功接受卡那单抗和 MCS 治疗的病例。本综述表明,心肌炎可能是 AOSD 患者并发症的早期阶段,AOSD 的严重程度可能与心肌炎的严重程度相关。卡那单抗治疗 AOSD 和 MCS 治疗暴发性心肌炎可能是克服合并症的选择之一。