急性髓系白血病患者t(6;20)(q13;q11.2)和额外的衍生染色体1涉及染色体14和1。

Jacob Rocha, Leah Gallagher, Alexandra Chu, Tahmeena Ahmed, Christina Giordano, Paula Fernicola, Htien Lee, Gabriela Evans, Carlos A Tirado
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引用次数: 0

摘要

目的:我们报告一例50岁男性急性髓性白血病(AML)。染色体分析显示异常核型为t(6;20)(q13;q11.2)和复杂重排导致额外的衍生染色体1 [der(1)(14q32->14p13::1p13->1q44],中期FISH证实。FISH分析证实30.5%[61/200]的细胞核中有一个额外的1q25拷贝。重排导致额外的1q拷贝在AML中很常见,但涉及6号和20号染色体的易位很少观察到。这两种情况以前在该患者中都见过,表明该患者的肿瘤持续存在。文献中只有6个病例描述了6号和20号染色体之间的易位。然而,在我们的患者[t(6;20)(q13;q11.2)]中发现的断点似乎是唯一的。需要进行进一步的研究来确定这是否是AML中常见/罕见的异常。此外,1号和14号染色体发生了复杂的重排,其特征是中期FISH,这仍然是临床细胞遗传学实验室检测复杂重排的有力工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Acute Myeloid Leukemia Patient with a t(6;20)(q13;q11.2) and an Extra Derivative Chromosome 1 Involving Chromosomes 14 and 1.

Objectives: We report the case of a 50-year-old male with acute myeloid leukemia (AML). Chromosome analysis revealed an abnormal karyotype with a t(6;20)(q13;q11.2) and a complex rearrangement leading to an extra derivative chromosome 1 [der(1)(14q32->14p13::1p13->1q44] which was confirmed by metaphase FISH. FISH analysis confirmed an extra copy of 1q25 in 30.5% [61/200] of the nuclei examined. Rearrangements leading to an extra copy of 1q are common in AML, but translocations involving chromosomes 6 and 20 are rarely observed. Both were seen previously in this patient, suggesting persistence of this patient's neoplasm. Only six cases in the literature describe translocations between chromosomes 6 and 20. However, the breakpoints found in our patient [t(6;20)(q13;q11.2)] appear to be unique. Further studies need to be conducted to determine if this is a common/rare abnormality in AML. Also, there was a complex rearrangement involving chromosomes 1 and 14, which was characterized by metaphase FISH, which is still a powerful tool for detecting complex rearrangements in the clinical cytogenetics laboratory.

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