朗格汉斯细胞组织细胞增多症：组织细胞协会当前建议综述
Langerhans cell histiocytosis: a review of the current recommendations of the Histiocyte Society.
作者信息
Satter Elizabeth K, High Whitney A
机构信息
Department of Dermatology, Naval Medical Center, San Diego, California 92134-2300, USA.
出版信息
Pediatr Dermatol. 2008 May-Jun;25(3):291-5. doi: 10.1111/j.1525-1470.2008.00669.x.
Langerhans cell histiocytosis is a rare proliferative disorder where pathologic Langerhans cells accumulate in a variety of organs. Historically, the nomenclature regarding this entity has been confusing because the disease had been subcategorized simply based upon the different clinical manifestations. In the following article, we summarize the current recommendation of the Histiocyte Society regarding the classification, evaluation, prognosis, and treatment of Langerhans cell histiocytosis.
朗格汉斯细胞组织细胞增多症是一种罕见的增殖性疾病，病理上朗格汉斯细胞在多种器官中积聚。从历史上看，关于这一实体的命名一直很混乱，因为该疾病只是简单地根据不同的临床表现进行了细分。在接下来的文章中，我们总结了组织细胞协会目前关于朗格汉斯细胞组织细胞增多症的分类、评估、预后和治疗的建议。
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