从儿童多系统炎症综合征到继发性嗜血细胞淋巴组织细胞增多症的一系列不幸事件:病例报告和文献综述。

Zahraa Mansoor, Ahmed Nugud, Walid Abuhammour, Lemis Yavuz, Ernestina Belt, Elsadeg Sharif
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引用次数: 0

摘要

儿童多系统炎症综合征(MIS-C)是最近描述的 COVID-19 大流行后的儿科疾病。嗜血细胞淋巴组织细胞增多症(HLH)是一种由巨噬细胞和 T 淋巴细胞不规则增殖引起的临床综合征。这两种疾病可以被认为是重叠的,尽管在文献中可以找到各自不同的标准。在此,我们报告了一名因输血感染恶性疟原虫疟疾而继发 HLH 的 MIS-C 后 COVID-19 患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From multisystem inflammatory syndrome in children to secondary hemophagocytic lymphohistiocytosis a series of misfortunate events: case report and review of literature.

Multisystem inflammatory syndrome of childhood (MIS-C) is a recently described entity in pediatrics post-COVID-19 pandemic. Hemophagocytic lymphohistiocytosis (HLH) is a clinical syndrome caused by an unregulated proliferation of macrophages as well as T lymphocytes. Both entities can be considered overlapping, although distinct criteria for each can be found in the literature. Herein, we report a patient with MIS-C post-COVID-19 infection, complicated with HLH secondary to Plasmodium falciparum malaria from a blood transfusion.

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