期刊文献+

获得性噬血细胞综合征研究进展 被引量:15

原文传递
导出
摘要 噬血细胞综合征(HPS)又称噬血细胞性淋巴组织细胞增多症(HLH),是由淋巴细胞和组织细胞非恶性增生,分泌大量炎性因子所引起的严重甚至致命的炎症状态,它分为两大类:原发性噬血细胞综合征和获得性噬血细胞综合征。原发性HPS发病年龄多〈2岁,大多伴有常染色体或性染色体隐性遗传。获得性HPS可出现于任何年龄阶段,以〉8岁多见,目前尚没有找到明确存在的免疫缺陷。
作者 王晓琳 王昭
出处 《中华医学杂志》 CAS CSCD 北大核心 2010年第14期1004-1006,共3页 National Medical Journal of China
  • 相关文献

参考文献17

  • 1Janka G.Familial and acquired hemophagocytic lymphohistiocytosis.Eur J Pediatr,2007,166:95-109.
  • 2Janka G.Hemophagocytic syndromes.Blood Rev,2007,21:245-253.
  • 3Fisman DN.Hemophagocytic syndromes and infection.Emerg Infect Dis,2000,6:601-608.
  • 4王旖旎,王昭,吴林,岑溪南,李渤涛,宁丰,段学章,李娟.多中心72例噬血细胞综合征诊疗分析[J].中华血液学杂志,2009,30(12):793-798. 被引量:98
  • 5Lee SW,Wang CY,Lee BJ,et al.Hemophagocytic syndrome in Miliary tuberculosis presenting with noncaseating granulomas in bone marrow and liver.J Formos Med Assoc,2008,107:495-499.
  • 6王学文.噬血细胞综合征的研究进展[J].临床肿瘤学杂志,2008,13(11):1042-1046. 被引量:25
  • 7Larroche C,Mouthon L.Pathogenesis of hemophagocytic syndrome (HPS).Autoimmunity Reviews,2004,3:69-75.
  • 8Filipovich AH.Hemophagocytic lymphohistiocytosis (HLH) and related disorders.Hematology Am Soc Hematol Educ Program,2009:127-131.
  • 9Okamoto M,Yamaguchi H,Isobe Y,et al.Analysis of triglyceride value in the diagnosis and treatment response of secondary hemophagocytic syndrome.Inter Med,2009,48:775-781.
  • 10Henter JI,Home AC,Egeler RM,et al.HLH-2004:Diagnostic and therapeutic guidelines for Hemophagocytic lymphohistiocytosis.Pediatr Blood Cancer,2007,48:124-131.

二级参考文献46

  • 1Henter JI, Home AC, Arico M, et al. HLH-2004 : diagnostic and therapeutic guidelines for hemophagoeytie lymphohistioeytosis [J]. Pediatr Blood Cancer, 2007, 48(1) : 124 -131.
  • 2Janka GE. Familial and acquired hemophagocytic lymphohistiocytosis[J]. Eur J Pediatr, 2007, 166( 1 ) : 95 - 109.
  • 3Imashuku S. Differential diagnosis of hemophagocytie syndrome: underlysing disorders and selection of the most effective treatment [J]. Int J Hematol, 1997, 66(1) : 135 -151.
  • 4Schneider EM, Lorenz I, MuUer-Rosenberger M, et al. Hemophagocytic lymphohistiocytosis is associated with deficiencies of cellular cytolysis but normal expression of transcripts relevant to killer-cell-induced apoptosis[ J]. Blood, 2002, 100 ( 11 ) : 2891 - 2898.
  • 5Takada H, Ohga S, Mizuno Y, et al. Oversecretion of IL-18 in haemophagocytie lymphohistioeytosis: a novel marker of disease activity[J]. BrJ Haematol, 1999, 106(1): 182-189.
  • 6de Saint Basile G, Fischer A. Defective cytotaxic granule-mediated cell death pathway impairs T lym-phocyte homeostasis [ J ]. Curr Opin Rheumatol, 2003, 15(4) : 436 -445.
  • 7Allen M, De Fusco C, Legrand F, et al. Familial hemophagocytic lymphohistiocytosis: how late can the onset be? [J]. Haematologica, 2001, 86(5) : 499 -503.
  • 8Stepp SE, Dufourcq-Lagelouse R, Le Deist F, et al. Perforin gene defects in familial hemophagocytic Lymphohistiocytosis [ J ]. Science, 1999, 286(5546) : 1957 - 1959.
  • 9Zur S U, Beutel K, Kolberg S, et al. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNCI3D, STXI1, and RAB27A[ J]. Hum Mutat, 2006, 27 ( 1 ) : 62 - 68.
  • 10Ueda I, Morimoto A, Inaba T, et al. Characteristic perforin gene mutations of haemophagocytie lymphohistiocytosis patients in Japan[J]. BrJ Haematol, 2003, 121(3) : 503 -510.

共引文献133

同被引文献95

引证文献15

二级引证文献41

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部