Langerhans cell histiocytosis

Dingbao Chen
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Abstract

Tumours derived from Langerhans cells (LCs) are divided into two main subgroups, according to the degree of cytological atypia and clinical aggressiveness: LC histiocytosis (LCH) and LC sarcoma. Both subgroups maintain the phenotypic profile and ultrastructural features of LCs. LCH is a clonal neoplastic proliferation of Langerhans-type cells that express CD1a, langerin, and S100 protein, showing Birbeck granules by ultrastructural examination. Here the clinicopathological of LCH will be discussed.
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朗格汉斯组织细胞增多症
根据细胞学非典型性和临床侵袭性的程度,源自朗格汉斯细胞(LCs)的肿瘤分为两个主要亚群:LC组织细胞增生症(LCH)和LC肉瘤。这两个亚群都保持了LCs的表型特征和超微结构特征。LCH是表达CD1a、langerin和S100蛋白的langerhans型细胞的克隆性肿瘤增生,超微结构检查显示Birbeck颗粒。本文将讨论LCH的临床病理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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