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Multi-System Inflammatory Syndrome in Children (MIS-C) Following SARS-CoV-2 Infection: Review of Clinical Presentation Hypothetical Pathogenesis and Proposed Management

机译:儿童多系统炎症综合征(MIS-C)追踪SARS-COV-2感染:临床介绍假设发病机制和建议管理综述

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摘要

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection may result in the multisystem inflammatory syndrome in children (MIS-C). The clinical presentation of MIS-C includes fever, severe illness, and the involvement of two or more organ systems, in combination with laboratory evidence of inflammation and laboratory or epidemiologic evidence of SARS-CoV-2 infection. Some features of MIS-C resemble Kawasaki Disease, toxic shock syndrome, and secondary hemophagocytic lymphohistiocytosis/macrophage activation syndrome. The relationship of MIS-C to SARS-CoV-2 infection suggests that the pathogenesis involves post-infectious immune dysregulation. Patients with MIS-C should ideally be managed in a pediatric intensive care environment since rapid clinical deterioration may occur. Specific immunomodulatory therapy depends on the clinical presentation. The relationship between the immune response to SARS-CoV-2 vaccines in development and MIS-C requires further study.
机译:严重急性呼吸综合征冠状病毒2(SARS-COV-2)感染可能导致儿童多系统炎症综合征(MIS-C)。 MIS-C的临床介绍包括发烧,严重疾病和两个或多个器官系统的参与,与SARS-COV-2感染的炎症和实验室或流行病学证据组合。 MIS-C的一些特征类似于川崎病,毒性休克综合征和次生血液淋巴管症/巨噬细胞活化综合征。 MIS-C对SARS-COV-2感染的关系表明,发病机制涉及发后的免疫失调。由于可能出现快速临床恶化,理想情况下,患有MIS-C的患者应该在儿科重症监护环境中进行管理。特异性免疫调节治疗取决于临床介绍。在开发和MIS-C中对SARS-COV-2疫苗的免疫应答之间的关系需要进一步研究。

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