Department of Medical Sciences, Uppsala University, Sweden.
Ups J Med Sci. 2013 Mar;118(1):42-5. doi: 10.3109/03009734.2012.744122.
Hemophagocytic lymphohistiocytosis (HLH) is an aggressive inflammatory syndrome that results from inappropriate activation of the immune system. HLH has a high mortality if not treated. We describe a case of a fulminant HLH, associated with a reactivation of an EBV infection. The patient responded well to steroid treatment.
噬血细胞性淋巴组织细胞增生症(HLH)是一种由免疫系统异常激活引起的侵袭性炎症综合征。如果不治疗,HLH 的死亡率很高。我们描述了一例暴发性 HLH,与 EBV 感染再激活相关。该患者对类固醇治疗反应良好。