家族性噬血细胞性淋巴组织细胞增生症伴胸腺发育不良1例

朱雪明, 金美芳, 王兴东, 李莺, 李晓忠

中国当代儿科杂志 ›› 2009, Vol. 11 ›› Issue (12) : 939-940.

PDF(1376 KB)
PDF(1376 KB)
中国当代儿科杂志 ›› 2009, Vol. 11 ›› Issue (12) : 939-940.
病例报告

家族性噬血细胞性淋巴组织细胞增生症伴胸腺发育不良1例

  • 朱雪明,金美芳,王兴东,李莺,李晓忠
作者信息 +

Familial hemophagocytic lymphohistiocytosis complicated by thymic dysplasia: a case report

  • ZHU Xue-Ming, JIN Mei-Fang, WANG Xin-Dong, LI Ying, LI Xiao-Zhong
Author information +
文章历史 +

摘要

Abstract

No abstvact available

引用本文

导出引用
朱雪明, 金美芳, 王兴东, 李莺, 李晓忠. 家族性噬血细胞性淋巴组织细胞增生症伴胸腺发育不良1例[J]. 中国当代儿科杂志. 2009, 11(12): 939-940
ZHU Xue-Ming, JIN Mei-Fang, WANG Xin-Dong, LI Ying, LI Xiao-Zhong. Familial hemophagocytic lymphohistiocytosis complicated by thymic dysplasia: a case report[J]. Chinese Journal of Contemporary Pediatrics. 2009, 11(12): 939-940
中图分类号: R596   

参考文献

[1]Gonzalo DH, Rodriguez G, Marcilla D. Diagnostic difficulties of the hemophagocytic lymphohistiocytosis(HLH) associated with the Epstein-Barr virus[J]. J Pediatr Hematol Oncol, 2007, 29(3):206-207.
[2]Gupta AA, Tyrrell P, Valani R, Benseler S, Abdelhaleem M, Weitzman S. Experience with hemophagocytic lymphohistiocytosis/macrophage activation syndrome at a single institution[J]. J Pediatr Hematol Oncol, 2009, 31(2):81-84.
[3]Henter JI, Horne A, Aricó M, Egeler RM, Filipovich AH, Imashuku S, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis[J]. Pediatr Blood Cancer, 2007, 48(2):124-131.
[4]Steinberg O, Yacobovich J, Dgany O, Kodman Y, Livni G, Rachmel A, et al. Prolonged course of familial hemophagocytic lymphohistiocytosis[J]. J Pediatr Hematol Oncol, 2006, 28(12):831-833.
[5]Filipovich AH. Hemophagocytic lymphohistiocytosis and related disorders[J]. Curr Opin Allergy Clin Immunol, 2006, 6(6):410-415.
[6]Stepp SE, Dufourcq-Lagelouse R, Le Deist F, Bhawan S, Certain S, Mathew PA, et al. Perforin gene defects in familial hemophagocytic lymphohistiocytosis[J]. Science, 1999, 286(5446):1957-1959.
[7]Feldmann J, Callebaut I, Raposo G, Certain S, Bacq D, Dumont C, et al. Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3)[J]. Cell, 2003, 115(4):461-473.
[8]zur Stadt U, Schmidt S, Kasper B, Beutel K, Diler AS, Henter JI, et al. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11[J]. Hum Mol Genet, 2005, 14(6):827-834.
[9]汤永民, 廖婵. 噬血细胞综合征的分子生物学基础及其发病机制[J]. 实用儿科临床杂志, 2006, 21(9):513-516.
[10]Henter JI, Elinder G, Ost A. Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society[J]. Semin Oncol, 1991, 18(1):29-33.


PDF(1376 KB)

Accesses

Citation

Detail

段落导航
相关文章

/