Department of Pediatrics, National Taiwan University Children's Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Division of Infectious Diseases, Department of Internal Medicine, China Medical University Hospital, China Medical University, Taichung, Taiwan; Department of Laboratory Medicine, China Medical University Hospital, China Medical University, Taichung, Taiwan; Ph.D Program for Aging, School of Medicine, China Medical University, Taichung, Taiwan; Departments of Laboratory Medicine and Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.
J Microbiol Immunol Infect. 2023 Apr;56(2):236-245. doi: 10.1016/j.jmii.2023.01.001. Epub 2023 Jan 16.
Multisystem inflammatory syndrome in children (MIS-C) is a dysregulated autoimmune-mediated illness in genetically susceptible patients following COVID-19 with an interval of 2-6 weeks. The median age of patients with MIS-C is 6-11 years. Most common manifestations are involvement of gastrointestinal tract, cardiovascular system, hematological system, and mucocutaneous system. Respiratory tract, neurological system, musculoskeletal system, and kidney are less frequently affected. Mucocutaneous manifestations and coronary artery abnormalities characteristic for Kawasaki disease (KD) may be observed in a significant proportion of MIS-C patients that may make the differential diagnosis be difficult for some patients, especially in the post-pandemic era. The mortality rate is 1-3%. Management and prognosis of MIS-C are similar to that of KD. MIS-C and KD may share a common pathogenic process. Based on the observation of MIS-C-like illness in uninfected neonates, i.e. multisystem inflammatory syndrome in neonates, both MIS-C and KD may be a consequence of dysregulated, over-exaggerated humoral immune responses triggered by a specific infectious agent.
儿童多系统炎症综合征(MIS-C)是一种在 COVID-19 后 2-6 周内具有遗传易感性的患者出现的失调性自身免疫介导疾病。MIS-C 患者的中位年龄为 6-11 岁。最常见的表现是胃肠道、心血管系统、血液系统和黏膜皮肤系统受累。呼吸道、神经系统、肌肉骨骼系统和肾脏较少受影响。MIS-C 患者中可观察到类似于川崎病(KD)的特征性黏膜皮肤表现和冠状动脉异常,这可能使某些患者的鉴别诊断变得困难,尤其是在后疫情时代。死亡率为 1-3%。MIS-C 的治疗和预后与 KD 相似。MIS-C 和 KD 可能具有共同的发病机制。基于对未感染新生儿即新生儿多系统炎症综合征的观察,MIS-C 和 KD 可能都是由特定感染因子触发的失调、过度夸大的体液免疫反应的结果。