Zhang Qian, Yan CunLiang, Xu Lei, Xie Wenyue, Li JinMeng, Zhang Wenli, Xu HaiChan, Zhang HongYu
Department of Hematology, Peking University Shenzhen Hospital, Road Lianhua #1120, Shenzhen, 518036 Guangdong China.
Department of Clinical Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036 Guangdong China.
Indian J Hematol Blood Transfus. 2021 Jan;37(1):90-95. doi: 10.1007/s12288-020-01308-6. Epub 2020 Aug 12.
Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening disease, which is characterized by severe systemic inflammation with cytokine storm as well as histologic evidence of hemophagocytosis. Besides, coagulopathy and hemorrhages are two common severe complications in HLH patients. Recent literatures indicate that Epstein-Barr virus (EBV) infection is one of the important triggers for the disease. In the study, we present three cases of EBV related HLH (EBV-HLH) with coagulopathy in patients with distinct backgrounds. Case 1 is a 45-year-old female diagnosed with EBV associated NK/T cell lymphoproliferative disorder (EBV-T/NK-LPD) and EBV-HLH. Case 2 is a 17-year-old male with a diagnosis of EBV-T-LPD and EBV-HLH. Case 3 is a 51-year-old male and also diagnosed with EBV-T-LPD and EBV-HLH. All cases were given with treatment with HLH-94 protocol, and the symptoms of the three patients improved. Furthermore, during the treatment, protamine, which has not been reported in the literature previously, was given to the three cases with EBV-HLH, and our results showed that after treatment with protamine, the coagulopathy and bleedings in these patients were improved rapidly. Unfortunately, the three patients relapsed soon and died despite intensive treatment. However, these cases suggest that protamine may serve as a potential treatment option for coagulation associated with EBV-HLH. Besides, the study helps us improve the understanding of the EBV-HLH related coagulation disorders, and provide a potential strategy for future treatment of the disease.
噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见且危及生命的疾病,其特征为伴有细胞因子风暴的严重全身炎症以及噬血细胞现象的组织学证据。此外,凝血病和出血是HLH患者常见的两种严重并发症。近期文献表明,爱泼斯坦-巴尔病毒(EBV)感染是该疾病的重要触发因素之一。在本研究中,我们呈现了3例背景各异的伴有凝血病的EBV相关HLH(EBV-HLH)患者。病例1是一名45岁女性,诊断为EBV相关NK/T细胞淋巴增殖性疾病(EBV-T/NK-LPD)和EBV-HLH。病例2是一名17岁男性,诊断为EBV-T-LPD和EBV-HLH。病例3是一名51岁男性,同样诊断为EBV-T-LPD和EBV-HLH。所有病例均采用HLH-94方案进行治疗,3例患者的症状均有改善。此外,在治疗过程中,我们对3例EBV-HLH患者使用了此前文献未报道过的鱼精蛋白,结果显示,使用鱼精蛋白治疗后,这些患者的凝血病和出血情况迅速改善。不幸的是,尽管进行了强化治疗,这3例患者很快复发并死亡。然而,这些病例提示鱼精蛋白可能是治疗与EBV-HLH相关凝血问题的一种潜在选择。此外,本研究有助于我们加深对EBV-HLH相关凝血障碍的理解,并为该疾病未来的治疗提供一种潜在策略。