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新冠病毒引发血栓性微血管病:病例报告。

Thrombotic Microangiopathy Triggered by COVID-19: Case Reports.

机构信息

Nephrology Sechenov First Moscow State Medical University, Moscow, Russian Federation.

Morphology Department, Evdokimov Moscow State University of Medicine and Dentistry, Moscow, Russian Federation.

出版信息

Nephron. 2022;146(2):197-202. doi: 10.1159/000520144. Epub 2021 Nov 22.

DOI:10.1159/000520144
PMID:34808629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8678244/
Abstract

SARS-CoV-2 causes thrombotic microangiopathy (TMA) through the activation of an alternative and lectin complement pathway. TMA is one of the main reasons for acute kidney injury development in patients with COVID-19. In this study, we present 3 TMA cases with severe kidney injury triggered by SARS-CoV-2. In the absence of other TMA causes, we diagnosed the atypical hemolytic uremic syndrome, triggered by SARS-CoV-2 due to abnormal complement activation. Because of both coagulation factors activation, and the high level of D-dimer in patients with COVID-19, it is crucial to differentiate disseminated intravascular coagulation from TMA. The use of anticomplement therapies such as eculizumab should be considered in refractory cases of progressive COVID-19. Controlled clinical trials are required before a definitive statement can be made.

摘要

SARS-CoV-2 通过激活替代途径和凝集素补体途径引起血栓性微血管病(TMA)。TMA 是 COVID-19 患者急性肾损伤发展的主要原因之一。在本研究中,我们介绍了 3 例由 SARS-CoV-2 引发的严重肾损伤的 TMA 病例。在没有其他 TMA 病因的情况下,由于补体异常激活,我们诊断为 SARS-CoV-2 引发的非典型溶血性尿毒症综合征。由于 COVID-19 患者的凝血因子激活和 D-二聚体水平升高,区分弥散性血管内凝血和 TMA 至关重要。对于进行性 COVID-19 的难治性病例,应考虑使用抗补体疗法,如依库珠单抗。在做出明确声明之前,需要进行对照临床试验。