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噬血细胞综合征30例临床分析 被引量:8

A clinical analysis of 30 patients with hemophagocytic syndrome
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摘要 目的:探讨噬血细胞综合征(HPS)的临床特点、诊断、治疗以及预后的危险因素。方法:对我院30例HPS患者的病因、临床表现、实验室检查指标、治疗方案及临床转归进行回顾性分析。结果:30例HPS病因以感染最多见(30%),其中EB病毒感染达20%,然而病因不明者也高达56.7%。HPS临床表现为持续高热(100%)、脾肿大(93.3%)、全血细胞减少(83.3%)、乳酸脱氢酶(100%)及血清铁蛋白(100%)升高。肝功能损害(90%)及心肌酶谱(60%)升高也较为常见。30例经治HPS患者30d、100d、1年的生存率分别为36.7%、23.3%、10.0%。其中7例给予包含VP16的化疗方案,30d、100d、1年的生存率分别为85.1%、71.4%、42.9%。结论:HPS可由多种病因所致,EB病毒最为常见,临床表现多样。发热、血清铁蛋白、乳酸脱氢酶升高在诊断中的灵敏度较高。包含VP16的化疗方案是有效的治疗方案。 Objective:To investigate the clinical features,diagnosis and treatment of hemophagocytic syndrome(HPS) and possible factors affecting prognosis.Method:A retrospective study was carried out to analyze the causes,clinical features,laboratory findings,treatment and clinical outcomes of 30 patients with HPS.Result:Infection was the most common underlying disease(30%),in which EB virus-associated HPS was predominant,accounting for 20%.However,the cause of HPS was unknown in 56.7% patients.HPS was clinically characterized by prolonged fever(100%),splenomegaly(93.3%),Cytopenias(83.3%) and other features including elevated Serum ferritin(100%) and lactate dehydrogenase(100%).Liver dysfunction(90%) and elevated cardiac enzyme levels(60%) were also frequently observed.Overall survival at 30 days,100 days and 1 years was 36.7%,23.3%,10% respectively for all the patients,while the rate was 85.1%,71.4%,42.9% for those using chemotherapy regimens containing etoposide.Conclusion:There are various underlying diseases and clinical manifestations for HPS.Prolonged fever,elevated Serum ferritin and lactate dehydrogenase are sensitive diagnostic indicators of HPS.We conclude that early administration of etoposide is effective in treating patients with HPS.
出处 《临床血液学杂志》 CAS 2011年第3期276-278,共3页 Journal of Clinical Hematology
关键词 噬血细胞综合征 治疗 依托泊苷 预后 hemophagocytic syndrome treatment etoposide prognosis
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  • 1HENTER J I, HOME A, AFICO M, et al. HLH-2004 : di- agnostic and therapeutic guidelines for hemophagocytic ly- mohohistiocytosis[J]. Pediatr Blood Cancer, 2007,48 : 124- 131. 被引量:1
  • 2JANKA G E. Familial and acquired hemophagocytic lym- phohistiocytosis[J]. Eur J Pediatr, 2007,166: 95- 109. 被引量:1
  • 3IMASHUKU S, HIBI S,OHARA T,et al. Effective control of Epstein-Barr virus related hemophagocytie lymphohistio- cytosis with imrnunochemotherapy [J]. Blood, 1999, 93: 1869-1874. 被引量:1
  • 4CHEN J S,LIN K H,LIN D T,et al. Longitudinal obser- vation and outcome of non-familial childhood haemophago- cytic syndrome receiving etoposide-containing regimens[J]. Br J Haematol,1998,103:756-762. 被引量:1
  • 5王兆俊,熊光华,管立人.新中国黑热病流行病学与防治成就[J].中华流行病学杂志,2000,21(1):51-54. 被引量:90
  • 6OST A, NILSSON-ARDNOR S, HENTER J I. Autopsy findings in 27 children with haemophagocytic lymphohistio- cytosis[J]. Histopathology, 1998,32 : 310- 316. 被引量:1
  • 7EMMENEGGER U,SCHAER D J,LARROCHE C,et al. Haemophagocytic syndromes in adults: current concepts and challenges ahead[J]. Swiss Med Wkly, 2005,135 : 299 -314. 被引量:1

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  • 1李国茹,段明,蒋朝东,李黎,李彦,张丽珍,兰艳华,张富南.重组抗原(rK39)试纸条诊断黑热病[J].寄生虫病与感染性疾病,2005,3(1):14-15. 被引量:15
  • 2Ishii E, Ohga S, Tanimur AM, et al. Clinical and epidemiologie studies of familial hemophagoeytie lymphohlstioeytosis in Japan. Japan LCH Study Group[J]. Med PedMtr Oneol, 1998,30: 276- 283. 被引量:1
  • 3Henter JI,Home A, Arico M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohlstiocytosis [J]. Pediatr Blood Cancer, 2007, 48(2) :124-131. 被引量:1
  • 4Fisman DN. Hemophagocytie syndrome and infeetion[J].Emerg InfeeDis, 2000, 6(6) :601-608. 被引量:1
  • 5Wong CK, Wong BC, Chan KC, et al. Cytokine profile infatal human immunodeficieney virus-tuberculosis EpsteinBarr Virus-as- sociated hemophagocytic syndrome[J].Arch Intern Med, 2007, 167(17):1901-1903. 被引量:1
  • 6Rouphael NG, Talati NJ, Vaughan C, et al. Infections associat- ed with haemophagocytie syndrome[J]. Lancet Infect Dis, 2007, 7(12) :814-822. 被引量:1
  • 7Song KS, Sung HI. Effect of plasma exchange on the circulating II.-6 levels in a patient with fatal hemophagocytic syndrome associated with bile ductopenia[J]. TherApher Dial, 2006, 10:87-89. 被引量:1
  • 8Janka G, zur Stadt U. Familial and acquired hemophagocytic lympho-histocytosis[ J]. Hematology Am Soc Hematol Educ Program,2005 :82-88. 被引量:1
  • 9Zur Stadt U, Beutel K, Kolberg S,et al. Mutation spectrum in childrenwith primary hemophagocytic lymphohistiocytosis ; molecular and func-tional analyses of PRF1, UNC13D, STX11,and RAB27A[ J]. HumMutat,2006,27(1) :62 -68. 被引量:1
  • 10Imashuku S. Clinical features and treatment strategies of Epstein - Burrvims - associated hemophagocytic lymphohistiocytosis [ J]. Crit Rev On-col Hematol, 2002,44(3) :259 -272. 被引量:1

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