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霍奇金病肿瘤细胞的核型畸变与表面标志物分析:1例报告并文献复习

Karyotype aberrations and surface marker analyses of the tumor cells of Hodgkin's disease: a case report and review of literature.

作者信息

Nagai M, Abe T, Seki S, Minato K, Watanabe S, Shimoyama M

出版信息

Jpn J Clin Oncol. 1986 Dec;16(4):397-406.

PMID:2432293
Abstract

Fresh tumor cells from pleural effusion of a patient with Hodgkin's disease were analyzed cytogenetically, immunologically and enzymocytochemically. They were characterized by the presence of alpha-naphthyl butyrate esterase activity, Fc gamma-receptor, HLA-DR antigen and No. 9 antigen which has been shown to be present in Hodgkin's cells and granulocytes, and the absence of definite T-, B- and myeloid cell markers. The karyotype analysis of these tumor cells revealed chromosome instability, but the clonality was confirmed by the many common abnormalities such as -4, -6, -10, -12, -13, -14, +21, del(X) (q22,q26), del(7) (q32q36), and +der(19)t(19;?). In addition, there were more duplicated tetraploid clones than near-diploid clones. The karyotype of the near-diploid clone was interpreted as: 48, X, del(X) (q22q26), -4, -6, -10, -12, -13, -14, +20, +21, +der(4)t(4;?) (p16;?), del(7) (q32q36), +der(19)t(19;?) (p13;?), +mar1, +mar2, +mar3. The karyotype abnormalities characteristic of lymphomas or leukemias were not found. These results indicate that the tumor cells are not of lymphoid or myeloid lineage. Further studies are needed to determine the cellular origin of the tumor cells of Hodgkin's disease.

摘要

对一名霍奇金病患者胸腔积液中的新鲜肿瘤细胞进行了细胞遗传学、免疫学和酶细胞化学分析。这些细胞的特征是存在α-萘丁酸酯酶活性、Fcγ受体、HLA-DR抗原以及已证实在霍奇金细胞和粒细胞中存在的9号抗原,并且缺乏明确的T、B和髓细胞标志物。对这些肿瘤细胞的核型分析显示染色体不稳定,但通过许多常见异常,如-4、-6、-10、-12、-13、-14、+21、del(X)(q22,q26)、del(7)(q32q36)和+der(19)t(19;?)证实了克隆性。此外,四倍体重复克隆比近二倍体克隆更多。近二倍体克隆的核型解释为:48,X,del(X)(q22q26),-4,-6,-10,-12,-13,-14,+20,+21,+der(4)t(4;?)(p16;?),del(7)(q32q36),+der(19)t(19;?)(p13;?),+mar1,+mar2,+mar3。未发现淋巴瘤或白血病特有的核型异常。这些结果表明肿瘤细胞不是淋巴样或髓样谱系。需要进一步研究以确定霍奇金病肿瘤细胞的细胞起源。

相似文献

1
Karyotype aberrations and surface marker analyses of the tumor cells of Hodgkin's disease: a case report and review of literature.霍奇金病肿瘤细胞的核型畸变与表面标志物分析:1例报告并文献复习
Jpn J Clin Oncol. 1986 Dec;16(4):397-406.
2
Chromosomes in Hodgkin's disease.
Cancer Treat Rep. 1982 Apr;66(4):639-43.
3
Hodgkin's disease, lymphocyte predominance type, nodular--a distinct entity? Unique staining profile for L&H variants of Reed-Sternberg cells defined by monoclonal antibodies to leukocyte common antigen, granulocyte-specific antigen, and B-cell-specific antigen.霍奇金病,淋巴细胞为主型,结节性——一种独特的实体?通过针对白细胞共同抗原、粒细胞特异性抗原和B细胞特异性抗原的单克隆抗体确定的里德-斯腾伯格细胞L&H变异型的独特染色特征。
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Chromosomal abnormalities in Hodgkin's disease.霍奇金淋巴瘤中的染色体异常。
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[Conversion of acute leukemia from a T-lymphoid to a myeloid phenotype].[急性白血病从T淋巴细胞表型向髓细胞表型的转化]
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Leu-M1--a marker for Reed-Sternberg cells in Hodgkin's disease. An immunoperoxidase study of paraffin-embedded tissues.Leu-M1——霍奇金病里德-斯腾伯格细胞的一种标志物。石蜡包埋组织的免疫过氧化物酶研究。
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Genomic instability and recurrent breakpoints are main cytogenetic findings in Hodgkin's disease.基因组不稳定和复发性断点是霍奇金淋巴瘤主要的细胞遗传学表现。
Haematologica. 1999 Apr;84(4):298-305.
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Immunopathology of Hodgkin's disease. Characterization of Reed-Sternberg cells with monoclonal antibodies.霍奇金病的免疫病理学。用单克隆抗体对里德-斯腾伯格细胞进行特征描述。
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[A T-cell type non-Hodgkin's lymphoma with a near-triploid karyotype].[一种具有近三倍体核型的T细胞型非霍奇金淋巴瘤]
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