期刊文献+

感染相关性噬血细胞综合征最新研究进展 被引量:5

原文传递
导出
摘要 近年来,随着对噬血细胞综合征研究的深入,对原发性噬血细胞综合征的发病机制有了较为全面的认识,但继发性噬血细胞综合征,尤其是感染相关性噬血细胞综合征的发病机制尚不明确。其发病机制可能与相关基因单核苷酸多态性及亚基因突变有关。感染相关噬血细胞综合征在临床中较其他类型噬血细胞综合征更为常见,且病情凶险,进展迅速,病死率高,早期诊断与鉴别诊断,及时及个体化治疗是成功治疗的关键。
出处 《中国实用医刊》 2015年第8期125-126,共2页 Chinese Journal of Practical Medicine
  • 相关文献

参考文献18

  • 1汤永民,徐晓军.噬血细胞性淋巴组织细胞增生症诊疗建议[J].中华儿科杂志,2012,50(11):821-825. 被引量:61
  • 2Ishii E, Ohga S, Imashuku S, et al ic lymphohistiecytosis in Japan[J]. Nationwide survey of hemophagocyt- Int J Hematol 2(107, 86(1) : 58-65.
  • 3Janka G, Imashuku S, Elinder G, et al. Infection-and malignancy-asso- ciated hemophagocytic syndromes: secondary hemophagecytic lymphohis- tiocytosis[J]. Hematol Oncol Clin North Am. 1998, 12(2) : 435-444.
  • 4徐晓军,汤永民.噬血细胞综合征诊治研究进展[J].中华儿科杂志,2011,49(9):712-716. 被引量:24
  • 5Castillo L, Carcillo J. Secondary hemophagocytic lymphohistiocytosis and severe sepsis/systemic inflammatory response syndrome/muhior- gan dysfunction syndrome/macrophage activation syndrome share com- mon intermediate phenotypes on a spectrum of inflammation[ J]. Pedi- atr Crit Care Med. 2009,10(3) :387-392.
  • 6Kejian Z, Michael B. Jordan, et al. Hypomorphic mutations in- PRF1, MUNC13-4 and STXBP2 are associated with adult-onset fa- milialHLH[J]. Blood, 2011,118(22): 5794-5798.
  • 7Kogawa K, Lee SM, Villanueva J, et al. Perforin expression in cyto- toxic lymphocytes from patients with hemophagocytic lymphohistiocyto- sis and their family members [ J]. Blood, 2002, 99 (1) : 61-66.
  • 8Henter JI, Horme A, Arico M, et al. HIH-2004 : diagnostic and thera- peutic guidelines for hemophagocytiI lymphohlstiocytosis [ J ]. Pediatr Blood Cancer,2007, 48 ( 2 ) : 124-131.
  • 9Henter JI, Home A, Arieo M, et al. HLH-2004 : Diagnostic and thera- peutic guidelines for hemophagoeytic lymphohistiocytosis [ J ]. Pediatr Blood Cancer,2007,48(2 ) : 124-131.
  • 10Bleesing J, Prada A, Siegel DM, et al. The diagnostic significance of soluble CD163 and soluble interleukin-2 receptor alpha-chain in mac- rophage activation syndrome and untreated new-onset systemic juvenile idiopathic arthritis[ J]. Arthritis Rheum, 2007, 56 (3) : 965-971.

二级参考文献60

  • 1郭霞,李强,周晨燕.儿童噬血细胞综合征41例临床分析[J].中华血液学杂志,2007,28(7):449-453. 被引量:26
  • 2Janka GE. Familial and acquired hemophagocytic lymphohistiocytosis. Eur J Pediatr, 2007 ; 166 : 95 - 109
  • 3Fautrel B, Le Moel G, Saint Marcoux B, et al. Diagnostic value of ferritin and glyeosylated fenitin in adult onset Still′s disease. J Rheumatol, 2001,28:322-329
  • 4Henter JI, Home AC, Arico M, et al. HLH-2004: diagnostic and Therapeutic Guidelines for Hemophagocytic Lymphohistioeytosis. Pediatr Blood Cancer, 2007 ; 48 : 124 - 131
  • 5Vignes S, Le-Moel G, Fautrel B, et al. Percentage of glycosylated serum ferritin remains low throughout the course of adult onset Stills disease. Ann Rheum Dis, 2000 ; 59 : 347 - 350
  • 6Allen CE, Yu X, Kozinetz CA, et al. Highly elevated ferritin levels and the diagnosis of hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer, 2008; 50:1227 -1235
  • 7Yamashita N, Oba K, Nakano H, et al. Age-related changes in concentrations of ferritin, glyeosylated ferritin, and non-glycosylated ferritin. Nippon Ronen Igakkai Zasshi, 1996; 33:754 -760
  • 8Henter JI, Elinder G, Soder O, et al. Hypercytokinemia in familial hemophagocytic lymphohistiocytosis. Blood, 1991,78 : 2918-2922.
  • 9Osugi Y, Hara J, Tagawa S, et al. Cytokine production regulating Thl and Th2 cytokines in hemophagocytic lymphohistiocytosis. Blood, 1997,89:4100-4103.
  • 10Tang Y, Xu X, Song H, et al. Early diagnostic and prognostic significance of a specific Thl/Th2 cytokine pattern in children with haemophagocytic syndrome. Br J Haematol, 2008,143:84-91.

共引文献118

同被引文献38

引证文献5

二级引证文献2

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