Nezelof C, Basset F
Department of Pathology, Faculté de Médecine de Paris, France.
Hematol Oncol Clin North Am. 1998 Apr;12(2):385-406. doi: 10.1016/s0889-8588(05)70518-9.
This article reviews the various investigative events that led to the endorsement of the term Langerhans cell histiocytosis for the various clinicopathologic conditions previously called Hand-Schüller-Christian disease, Abt-Letterer-Siwe disease, eosinophilic granuloma of bone, and histiocytosis X. The different denominations reflect the changing conceptual approaches to the so-called reticuloendothelial system and the successive acquisition of new ultrastructural and immunocytochemical data.
本文回顾了一系列研究事件，这些事件促使“朗格汉斯细胞组织细胞增多症”这一术语被用于指代先前被称为汉-许-克病、勒-雪病、骨嗜酸性肉芽肿和组织细胞增多症X的各种临床病理状况。不同的命名反映了对所谓网状内皮系统概念的不断变化，以及新的超微结构和免疫细胞化学数据的相继获得。
