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组织细胞增生病—x,主要指勒—雪氏病(Letterer—Siwe 病),韩—薛—柯氏病(Haud—Schüller—chrislian 病),及嗜酸性肉芽肿(eosiuophilic granuloma)。Beare 于1972年将组织细胞增生病—x 分为:(1)慢性进行性:韩—薛—柯氏病(2)急性播散性:勒—雪氏病(3)良性局限性:嗜酸性肉芽肿并将播散性黄色瘤,漫性扁平黄色瘤,幼年黄色肉芽肿,组织细胞瘤,全身发疹性组织细胞瘤,及网状内皮组织细胞瘤均归类于此。这些病十分少见,其症状体征的准确分类常有困难,在临症上多被认为是属于一个疾病的不同表现。少数病例的表现,常超过
Histiocytosis-x, predominantly refers to Letterer-Siwe disease, Haud-Schüller-chrislian disease, and eosiuophilic granuloma. Beare divided histiocytosis-x in 1972 into: (1) Chronic progressive: Hamster-Kirch disease (2) Acute disseminated: Leuchee’s disease (3) Benign limitations: Eosinophilic Granulomas and disseminated disseminated xanthoma, diffuse flat yellow tumor, juvenile yellow granuloma, histiocytoma, systemic erosive histiocytoma, and reticuloendothelial cell tumor are classified here. These diseases are very rare, the exact classification of the symptoms and signs are often difficult, in the clinical symptoms are mostly considered to belong to a different manifestation of a disease. A few cases of performance, often over