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机构地区:[1]北京医科大学口腔医学院
出 处:《中华口腔医学杂志》1998年第1期15-17,共3页Chinese Journal of Stomatology
摘 要:目的研究慢性局限性郎格罕细胞组织细胞增生症(Langerhanscelhistiocytosis,LCH)的组织病理学及免疫组织化学特点。方法HE染色及组织学观察,有丝分裂计数和免疫组织化学染色。结果本项研究包括22例LCH。HE染色见郎格罕细胞(LC)核因扭曲而呈现多样性,核分裂并不少见(平均每10个高倍视野7.1个核分裂像)。片状排列的细胞间可见明显不规则的细胞间隙。免疫染色见LCS-100阳性,增殖细胞核抗原(PCNA)阳性率平均为14.5%,病变中还散在CD68及组织蛋白酶D阳性的组织细胞,淋巴细胞以T细胞为主。结论上述结果提示,LC细胞核形态的多样性及细胞排列是诊断本病的基础;该病变的性质是LC增殖而不是LC单纯聚积,可能属于肿瘤性增生;病变中的LC属不成熟的LC前体细胞。Objective To investigate the pathological and immunohistochemical characteristics of chronic localized Langerhans cell histiocytosis (LCH). Methods HE staining and histopathological observation, mitotic counting and immunohistochemical staining. Results 22 cases of LCH were included in this study. The most prominent histologic feature was nuclear polymorphism of Langerhans cells (LC). Nuclear sulcus was often noted. Intercellular spaces were also obvious. Mitotic figures were commonly seen (the mean mitotic index was 7.1 under 10 high magnification fields). The mean PCNA index of LC was 14.5%. Other histiocytes and multinuclear cells were CD68 and cathepsin D positive. Conclusion The nuclear polymorphism of LC is of diagnostic value for LCH; LC in the lesions is hyperplastic and neoplastic in nature rather than simple accumulation and the S 100 positive LC are immature precursors of Langerhans cell.
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