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朗格罕斯细胞组织细胞增生症的造血干细胞移植治疗 被引量：4

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摘要 朗格罕斯细胞组织细胞增生症（Langerhans cell histiocytosis,LCH）是一种发病机制尚未完全明了的组织细胞病。正是因为发病机制未完全阐明,长期以来对LCH的治疗均基于经验的积累。尽管治疗的根本措施改进甚少,但由于支持治疗的进步,最初6周诱导未获得良好治疗反应的患者均重复进行诱导治疗。
作者 吴南海
机构地区 海军总医院儿科
出处 《中国小儿血液与肿瘤杂志》 CAS 2014年第5期230-232,共3页 Journal of China Pediatric Blood and Cancer
关键词 造血干细胞移植 HISTIOCYTOSIS LANGERHANS 细胞病 脐血移植 发病机制 混合嵌合状态 髓细胞 骨髓分析 造血前体细胞
分类号 R725.9 [医药卫生—儿科]
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参考文献17

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同被引文献21

  • 1高巧娣,陆凤娟,吴长根,马伴吟,吴玥.小儿郎格罕细胞组织细胞增生症32例临床分析[J].临床儿科杂志,2005,23(2):94-97. 被引量：8
  • 2盛光耀.朗格汉斯细胞组织细胞增生症[M].//王卫平.儿科学.8版.北京:人民卫生出版社,2013:384-387.
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  • 4Lee S K, Jung T Y, Jung S, et al. Solitary Langerhans cell histocytosis of skull and spine in pediatric and adult patients [J ]. Childs Nerv Syst,2014,30(2) :271-275.
  • 5Garg A, Kumar P. Multisystem Langerhans cell histioeytosis in adult [ J]. Indian J Dermato1,2012,57 (1) :58-60.
  • 6Yashoda-Devi B, Rakesh N, Agarwal M. Langerhans cell histiocytosis with oral manifestations: a rare and unusual case report [J]. J Clin Exp Dent,2012,4 (4) :e252-e255.
  • 7Lajolo C, Campisi G, Deli G, et al. Langerhans' s cell bistiocytosis in old subjects: Two rare case reports and review of the literature[J]. Gerodontology,2012,29(2) :e1207-e1214.
  • 8Funk R K, Ferraro D J, Perrin R J, et al. Recurrent adult-onset hypophyseal Langerhans cell histiocytosis after radiotherapy: a case report[J]. J Med Case Rep,2012,6:341.
  • 9Herwig M C, Wojno T, Zhang Q, et al. Langerhans cell histiocytosis of the orbit: five clinicopathologic cases and review of the literature[J]. Surv Ophthalmol,2013,58(4) :330-340.
  • 10Atalay F, Koc E A, Yildiz S. A rare presentation of langerhans cell histiocytosis tonsil infiltration: review of the literature: atypical presentation of langerhans cell histiocytosis [ J ]. Indian J Hernatol Blood Transfus ,2014,30 ( Suppl 1 ) :437-439.

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中国小儿血液与肿瘤杂志
2014年 第5期

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