朗格罕斯细胞组织细胞增多症发病机制及治疗  

Langerhans cell histiocytosis:pathology and treatment

作　　者：刘子勤[1] 王天有[1] 

机构地区：[1]首都儿科研究所,北京100020

出　　处：《临床儿科杂志》2009年第8期709-713,共5页Journal of Clinical Pediatrics

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.

关 键 词：朗格罕斯细胞组织细胞增多症 发病机制 治疗 

分 类 号：R725.5[医药卫生—儿科]