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本病是一组病因不明,以组织细胞过度增生为主要病理特征的疾病。“X”表示病因不明。临床上可分为三种疾病或综合征,即勒-雪氏病(Letterer—Siwe’s disease),又称婴儿型组织细胞增生症;韩-雪-柯氏病(Hand-Schuller-christian’s disease),又称黄脂瘤或儿童型组织细胞增生症及嗜酸性肉芽肿(Eosinophilic granuloma)。对其总的命名及三种综合征之间的关系至今尚有分歧。此病最早是Hand氏在1893年报告的,国内胡用霖
The disease is a group of unknown etiology, to organize cell hyperplasia as the main pathological features of the disease. \"X\" indicates the cause is unknown. Clinically, there are three types of diseases or syndromes, namely, Letterer-Siwe\'s disease, also known as infantile histiocytosis; Hand-Schuller-christian\'s disease, Also known as yellow lipoma or childhood histiocytosis and eosinophilic granuloma. The overall naming and the relationship between the three syndromes are still divisive. The earliest disease is Hand\'s report in 1893, the domestic Hu Lin