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外周T细胞淋巴瘤的分类:细胞遗传学研究结果支持更新后的基尔分类法。

Classification of peripheral T-cell lymphomas: cytogenetic findings support the updated Kiel classification.

作者信息

Schlegelberger B, Feller A C

机构信息

Department of Human Genetics, University of Kiel, Germany.

出版信息

Leuk Lymphoma. 1996 Feb;20(5-6):411-6. doi: 10.3109/10428199609052422.

Abstract

The cytogenetic findings in peripheral T-cell lymphomas enabled us to distinguish not only between low and high grade peripheral T-cell lymphomas (PTL) but also between different morphologically defined subtypes. High grade lymphomas exhibited a higher frequency of aberrant clones, polyploid chromosome numbers, a higher complexity of aberrant clones and a lower proportion of normal metaphases than low grade PTL. Moreover, deletions in 6q, trisomies of 7q and monosomy 13 or changes of 13q14 were significantly more frequent in high grade than in low grade PTL. Translocation t(2;5)(p23;q35) was only seen in large cell anaplastic lymphoma. T-CLL/T-PLL was associated with the simultaneous presence of inversion inv(14)(q11q32.l) and trisomy 8q, mostly due to i(8q)(q10). Trisomy 3 was a characteristic chromosome aberration of lymphoepithelioid lymphoma, AILD-type T-cell lymphoma and T-zone lymphoma. In contrast to the other low grade PTL, AILD-type T-ceIl lymphoma and cutaneous T-cell lymphoma showed a high frequency of unrelated clones. In summary, the cytogenetic findings paralleled the histopathologic classification according to the updated Kiel classification and support the value of the distinction of the different morphologically defined entities.

摘要

外周T细胞淋巴瘤的细胞遗传学研究结果使我们不仅能够区分低级别和高级别外周T细胞淋巴瘤(PTL),还能区分不同形态学定义的亚型。与低级别PTL相比,高级别淋巴瘤异常克隆的频率更高、多倍体染色体数目更多、异常克隆的复杂性更高且正常中期相的比例更低。此外,6q缺失、7q三体和13号染色体单体或13q14改变在高级别PTL中显著比低级别PTL更常见。易位t(2;5)(p23;q35)仅见于间变性大细胞淋巴瘤。T细胞慢性淋巴细胞白血病/ T细胞幼淋巴细胞白血病与inv(14)(q11q32.1)倒位和8q三体同时存在相关,主要是由于i(8q)(q10)。3号染色体三体是淋巴上皮样淋巴瘤、AILD型T细胞淋巴瘤和T区淋巴瘤的特征性染色体畸变。与其他低级别PTL不同,AILD型T细胞淋巴瘤和皮肤T细胞淋巴瘤显示出高频的不相关克隆。总之,细胞遗传学研究结果与根据更新的基尔分类法进行的组织病理学分类相一致,并支持区分不同形态学定义实体的价值。

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