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朗格罕斯细胞组织细胞增多症发病机制及治疗 被引量:5

Langerhans cell histiocytosis:pathology and treatment
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摘要 朗格罕斯细胞组织细胞增多症是一种少见病,大量朗格罕斯细胞组织聚集于多种脏器,导致不同的临床表现,但其发病机制尚未完全阐明。文章将该病发病机制及治疗作一阐述,以提高临床医师对该病的认识。 Langerhans cell histiocytosis (LCH) is a rare proliferative disorder with pathologic Langerhans cells accumulate in a variety of organs and causes various clinical presentations. The pathogenesis of LCH has not been clarified. The current study of pathology and treatment of LCH were summarized in this article.
机构地区 首都儿科研究所
出处 《临床儿科杂志》 CAS CSCD 北大核心 2009年第8期709-713,共5页 Journal of Clinical Pediatrics
关键词 朗格罕斯细胞组织细胞增多症 发病机制 治疗 Langerhans cell histiocytosis pathology treatment
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参考文献32

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同被引文献42

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  • 2马鸣,黄晓磊,陈洁.郎格罕细胞组织细胞增生症继发硬化性胆管炎一例[J].中华儿科杂志,2006,44(4):311-312. 被引量:2
  • 3王宏胜,李军,马伴吟,高怡瑾,陆凤娟,钱晓文.改良DAL-HX83/90方案治疗儿童郎格罕细胞组织细胞增生症24例疗效观察[J].中国小儿血液与肿瘤杂志,2007,12(2):60-63. 被引量:12
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