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Hyperferritinemia in the critically ill child with secondary hemophagocytic lymphohistiocytosis/sepsis/multiple organ dysfunction syndrome/macrophage activation syndrome: what is the treatment?

机译:重症儿童继发性吞噬性淋巴细胞组织细胞增生/败血症/多器官功能障碍综合征/巨噬细胞活化综合征的高铁蛋白血症:治疗方法是什么?

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摘要

IntroductionHyperferritinemia is associated with increased mortality in pediatric sepsis, multiple organ dysfunction syndrome (MODS), and critical illness. The International Histiocyte Society has recommended that children with hyperferritinemia and secondary hemophagocytic lymphohistiocytosis (HLH) or macrophage activation syndrome (MAS) should be treated with the same immunosuppressant/cytotoxic therapies used to treat primary HLH. We hypothesized that patients with hyperferritinemia associated secondary HLH/sepsis/MODS/MAS can be successfully treated with a less immunosuppressant approach than is recommended for primary HLH.
机译:简介高铁蛋白血症与小儿败血症,多器官功能障碍综合征(MODS)和重症疾病的死亡率增加有关。国际组织细胞协会建议,患有高铁蛋白血症和继发性吞噬性淋巴细胞组织细胞增生症(HLH)或巨噬细胞活化综合征(MAS)的儿童应采用与治疗原发性HLH相同的免疫抑制剂/细胞毒性疗法进行治疗。我们假设与高铁蛋白血症相关的继发性HLH /败血症/ MODS / MAS患者可以用比原发性HLH少的免疫抑制剂方法成功治疗。

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