1例肉芽肿病合并多血管炎患者的COVID-19:处理策略

E. F. Iskhakova, E. Sukhorukova, M. Y. Badeeva, E. Dyakova, S. Lapshina, T. Beketova, D. Abdulganieva
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引用次数: 0

摘要

在2019冠状病毒病(COVID-19)大流行期间,anca相关性血管炎(AAV)患者会引起极度警觉,这与许多因素有关:呼吸系统(上呼吸道、肺部)和肾脏的初始损伤、免疫抑制治疗、COVID-19预后困难以及AAV恶化的风险。我们报告一例中度COVID-19临床病例,患者肉芽肿病合并多血管炎,长期接受利妥昔单抗(RTX)抗b细胞治疗。冠状病毒肺炎在RTX后一年出现,而b淋巴细胞持续耗竭。为了获得充分的抗病毒免疫反应和预防高发炎症,我们使用抗病毒药物、抗凝剂、恢复期血浆、人正常免疫球蛋白和白细胞介素-6拮抗剂托珠单抗进行治疗。讨论了AAV患者重症COVID-19的可能预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COVID-19 in a patient with granulomatosis with polyangiitis: Management tactics
Patients with ANCA-associated vasculitis (AAV) cause extreme alertness during the coronavirus disease 2019 (COVID-19) pandemic, associated with many factors: the initial damage to the respiratory system (upper respiratory tract, lungs) and kidneys, immunosuppressive treatments, difficult prognosis of COVID-19 with the risk of AAV exacerbation. We present a clinical case of а moderate COVID-19 in a patient with granulomatosis with polyangiitis, who received anti-B cell therapy with rituximab (RTX) for a long time. Coronavirus pneumonia developed one year after RTX, while B-lymphocyte depletion persisted. In order to achieve an adequate antiviral immune response and prevent hyperinflammation, treatment was carried out with antiviral drugs, anticoagulants, convalescent plasma, human normal immunoglobulin, and interleukin-6 antagonist tocilizumab. Possible predictors of severe COVID-19 in patients with AAV are discussed.
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