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首页> 外文期刊>International journal of dermatology >Two case report studies of Langerhans cell histiocytosis with an analysis of 918 patients of Langerhans cell histiocytosis in literatures published in China.
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Two case report studies of Langerhans cell histiocytosis with an analysis of 918 patients of Langerhans cell histiocytosis in literatures published in China.

机译：在中国发表的两篇有关朗格汉斯细胞组织细胞增生症的病例报告研究中，对918名朗格汉斯细胞组织细胞增生症患者进行了分析。

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摘要

Langerhans Cell Histiocytosis (LCH), which was previously designated histiocytosis X, is a group of diseases characterized as hyperplasia and dissemination of Langerhans cells. LCH may involve one or many body systems or tissues, such as skin, lymph nodes, bone, bone marrow, liver, spleen, lung, thymus, gastrointestine, endocrine gland, mouth, ears, and central nervous system. The clinical manifestation of this group of diseases varies from single organ to multiple organs, from newborn to the old, and is especially highly prevalent among children1. LCH has been recognized as a rare disease in the past, whereas the incidence has significantly increased in recent years with the progress in diagnostic techniques. To summarize the feature of skin lesions in LCH, we present a retrospective clinical analysis of two patients with LCH diagnosed in our hospital and another 916 cases reported in China over the past 10 years.
机译：朗格汉斯细胞组织细胞增生症（LCH），以前称为组织细胞增生症X，是一组以朗格汉斯细胞增生和扩散为特征的疾病。 LCH可能涉及一个或多个身体系统或组织，例如皮肤，淋巴结，骨骼，骨髓，肝脏，脾脏，肺，胸腺，胃肠道，内分泌腺，口腔，耳朵和中枢神经系统。这组疾病的临床表现从单个器官到多个器官，从新生儿到老年人都有，在儿童中尤为普遍。过去，LCH被认为是一种罕见疾病，但是随着诊断技术的进步，近几年来LCH的发病率显着增加。为了总结LCH皮肤病变的特征，我们对过去十年来在我院诊断的两名LCH患者和中国报告的916例患者进行了回顾性临床分析。

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