灾难性抗磷脂综合征:发病机制、诊断和治疗的现状

A. Klimenko, A. Gaffarova, N. Demidova
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引用次数: 0

摘要

灾难性抗磷脂综合征(CAPS)是一种危及生命的疾病,与微血管血栓性闭塞的发展有关,死亡率约为50%。CAPS的发病机制是基于细胞活化、补体系统诱导、细胞因子刺激、抗凝因子抑制和纤维蛋白溶解,从而导致进行性血栓性微血管病变、弥散性血管内凝血(DIC)和全身炎症反应综合征。CAPS的分类标准包括:微血栓性累及≥3个器官(最常见的是肺、肾脏和中枢神经系统)≤1周,且抗磷脂抗体滴度高。鉴别诊断为DIC、肝素性血小板减少症、溶血性尿毒症综合征、HELLP综合征、败血症。急性期CAPS的治疗包括抗凝和免疫抑制治疗(糖皮质激素、血浆置换、静脉免疫球蛋白、利妥昔单抗、eculizumab)。及时诊断和适当选择治疗可将死亡率从50%降低到30%。为了改善患者的预后和延长患者的预期寿命,需要对CAPS进行进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Catastrophic antiphospholipid syndrome: current aspects of pathogenesis, diagnosis and treatment
Catastrophic antiphospholipid syndrome (CAPS) is a life-threatening condition associated with the development of thrombotic occlusion of microvasculature vessels, with a mortality rate of about 50%.The pathogenesis of CAPS is based on cellular activation, complement system induction, cytokine stimulation, inhibition of anticoagulant factors and fibrinolysis, which leads to progressive thrombotic microangiopathy, disseminated intravascular coagulation (DIC), and systemic inflammatory response syndrome. Classification criteria for CAPS include microthrombotic involvement of ≥3 organs (most commonly lungs, kidneys, and central nervous system) for ≤1 week with high titers of antiphospholipid antibodies.Differential diagnosis is carried out with DIC, heparin-induced thrombocytopenia, hemolytic uremic syndrome, HELLP syndrome, sepsis. Treatment of CAPS in the acute phase involves anticoagulant and immunosuppressive therapy (glucocorticoids, plasmapheresis, IV immunoglobulin, rituximab, eculizumab). Timely diagnosis and adequately selected treatment of CAPS can reduce mortality from 50 to 30%.Further study of CAPS is needed to improve the prognosis and increase the life expectancy of patients.
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