COVID-19后成人发病Still's病1例报告及文献复习

IF 0.9 Q4 RHEUMATOLOGY
Tsubasa Maeda, Goshi Komine, Ryosuke Noda, Mikiya Komatsu, Mariko Sakai, Yukiko Takeyama, Sachiko Soejima, Akihito Maruyama, Mitsuteru Akahoshi, Syuichi Koarada, Yoshifumi Tada
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引用次数: 0

摘要

一名59岁男子在感染COVID-19后11天出现成人发病斯蒂尔氏病。患者表现为高烧、多发性关节炎、红斑、喉咙痛、c反应蛋白和铁蛋白水平高;糖皮质激素和甲氨蝶呤治疗导致疾病缓解。我们回顾了12例成人发病的COVID-19后Still病的临床特征(文献11例,本病例11例)。8例为女性,中位年龄为54岁(19-59岁),从COVID-19到斯蒂尔病发病的中位时间为12.5天。高热、关节痛、典型皮肤病变、喉咙痛、肝损伤和中性粒细胞计数增加的频率与非冠状病毒相关的成人发病斯蒂尔氏病的病例没有差异。所有病例血清铁蛋白水平均升高(中位数为6354 ng/mL)。并发症很少,有一例巨噬细胞激活综合征。免疫抑制药物和生物制剂分别应用5例和3例,均取得良好疗效。我们的综述表明,成人发病的Still's病在COVID-19后发展早期,临床表现与非COVID-19相关病例相似,严重并发症很少,预后良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adult-onset Still's disease following COVID-19: A case report and literature review.

A 59-year-old man developed adult-onset Still's disease 11 days after contracting COVID-19. He presented with high fever, polyarthritis, erythema, sore throat, and high levels of C-reactive protein and ferritin; treatment with glucocorticoids and methotrexate led to disease remission. We reviewed the clinical characteristics of 12 cases (11 from the literature and the present case) of adult-onset Still's disease following COVID-19. Eight cases involved females, with a median age of 54 years (19-59 years), and the median time from COVID-19 to Still's disease onset was 12.5 days. Frequencies of high fever, arthralgia, typical skin lesion, sore throat, liver damage, and increased neutrophil count did not differ from cases of non-COVID-related adult-onset Still's disease. Serum ferritin levels were increased in all cases (median 6,354 ng/mL). Complications were infrequent, with macrophage activation syndrome reported in one case. Immunosuppressive drugs and biologic agents were used in five and three cases, respectively, and all cases had good outcomes. Our review suggests that adult-onset Still's disease develops early after COVID-19, presenting with clinical findings similar to non-COVID-19-related cases, and has few severe complications and a good prognosis.

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