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非皮肤外周T细胞淋巴瘤中的细胞遗传学异常

Cytogenetic abnormalities in noncutaneous peripheral T-cell lymphoma.

作者信息

Sanger W G, Weisenburger D D, Armitage J O, Purtilo D T

出版信息

Cancer Genet Cytogenet. 1986 Sep;23(1):53-9. doi: 10.1016/0165-4608(86)90149-4.

Abstract

Cytogenetic studies were performed on lymph nodes from eight patients with noncutaneous peripheral T-cell lymphoma. At least one chromosomally abnormal clone was identified in each patient. Chromosomes having structural abnormalities in two or more patients included chromosome #1 (four), chromosome #2 (three), chromosome #4 (two), chromosome #8 (two), chromosome #14 (two), and chromosome #17 (two). The abnormal clones from seven patients had structural abnormalities involving either chromosomes #1 or #2, and the eighth patient had an abnormal clone that was trisomic for chromosome #1. We did not observe structural rearrangements in chromosome #14 at bands q11 or q12 in any of our cases, in contrast to previous suggestions that this chromosomal region may play a critical role in the development of T-cell lymphomas. Our findings suggest that other nonrandom chromosome abnormalities are common and may be important in the development of noncutaneous peripheral T-cell lymphomas.

摘要

对8例非皮肤外周T细胞淋巴瘤患者的淋巴结进行了细胞遗传学研究。每位患者至少鉴定出一个染色体异常克隆。在两名或更多患者中存在结构异常的染色体包括1号染色体(4例)、2号染色体(3例)、4号染色体(2例)、8号染色体(2例)、14号染色体(2例)和17号染色体(2例)。7例患者的异常克隆具有涉及1号或2号染色体的结构异常,第8例患者有一个异常克隆,该克隆为1号染色体三体。与之前认为该染色体区域可能在T细胞淋巴瘤发生中起关键作用的观点相反,我们的任何病例中均未观察到14号染色体q11或q12带的结构重排。我们的研究结果表明,其他非随机染色体异常很常见,可能在非皮肤外周T细胞淋巴瘤的发生中起重要作用。

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