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系统性毛细血管渗漏综合征2例的治疗体会 被引量:4

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摘要 系统性毛细血管渗漏综合征(systemic capillary leak syndrome,SCLS)为临床罕见病例,主要表现为反复发作的全身性水肿、严重的低血容量性低血压、休克、低蛋白血症等症状,且伴随着毛细血管的严重高渗状态。最早由Clarkson等-([1])于1960年报道,关于其发病机制不详,认为主要与补体、白细胞介素-2、白三烯等细胞因子有关。我们在近年工作中遇到2例,且均治疗成功,报道如下。
出处 《内科急危重症杂志》 2017年第1期72-73,79,共3页 Journal of Critical Care In Internal Medicine
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