Xiao Li, Xian Ying, Dai Bi-tao, Su Yong-chun, Xiao Jian-wen, Zheng Qi-cheng, Zhao Xiao-dong, Yu Jie
Department of Hemooncology, Chongqing Medical University, Chongqing, China.
Zhonghua Xue Ye Xue Za Zhi. 2011 Oct;32(10):668-72.
To investigate the clinical features of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis (EBV-HLH), to analysis the outcome of HLH-2004 protocol, and to explore the prognostic factors in EBV-HLH patients.
The clinical features at onset and outcome of HLH-2004 protocol from 83 pediatric patients with EBV-HLH enrolled from January 2006 to December 2009 in our hospital were analyzed retrospectively. Univariate and multivariate COX regression analysis were used to identify statistically significant prognostic factors.
(1) Among the 83 patients, 45 were males and 38 were females. The age of onset ranged from 6 months to 14 years 4 months. 44 patients were treated with HLH-2004, and 3-year overall survival (OS) was (55.8 ± 7.9)%. (2) The most common clinical features of EBV-HLH included high fever, cytopenia, hepatosplenomegaly, and coagulopathy; The respiratory symptoms, angina phlogistic, skin rashes, neurologic abnormality were rare. 97.3% of patients showed an elevation of serum ferritin, liver dysfunction and lipid metabolism disorders was found in most of EBV-HLH patients. 89.0% of patient had hemophagocytosis in bone marrow at diagnosis of EBV-HLH. (3) COX regression analysis revealed that anemia degree, serum albumin < 30 g/L, CD4:CD8 abnormity, NK cell < 3%, treatment protocol were related with the prognosis significantly (P < 0.05).
EBV-HLH in pediatric patients has severe clinical feature and poor prognosis. HLH-2004 protocol is an effective treatment for patients with EBV-HLH. Symptomatic treatment can't rescue the patients of EBV-HLH.
探讨爱泼斯坦-巴尔病毒相关噬血细胞性淋巴组织细胞增生症(EBV-HLH)的临床特征,分析HLH-2004方案的治疗效果,并探索EBV-HLH患者的预后因素。
回顾性分析2006年1月至2009年12月我院收治的83例小儿EBV-HLH患者采用HLH-2004方案治疗的起病时临床特征及治疗效果。采用单因素和多因素COX回归分析确定具有统计学意义的预后因素。
(1)83例患者中,男45例,女38例。发病年龄为6个月至14岁4个月。44例患者采用HLH-2004方案治疗,3年总生存率为(55.8±7.9)%。(2)EBV-HLH最常见的临床特征包括高热、血细胞减少、肝脾肿大和凝血功能障碍;呼吸道症状、咽峡炎、皮疹、神经异常少见。97.3%的患者血清铁蛋白升高,大多数EBV-HLH患者存在肝功能障碍和脂质代谢紊乱。89.0%的患者在EBV-HLH诊断时骨髓中有噬血细胞现象。(3)COX回归分析显示,贫血程度、血清白蛋白<30 g/L、CD4:CD8异常、NK细胞<3%、治疗方案与预后显著相关(P<0.05)。
小儿EBV-HLH临床特征严重,预后差。HLH-2004方案是治疗EBV-HLH患者的有效方法。对症治疗不能挽救EBV-HLH患者。