一种罕见的近四倍体核型的t细胞成人急性淋巴细胞白血病

IF 0.1 Q4 HEMATOLOGY
Vrushali Raut, H. Khurana, Barun K. Chakrabarty, B. Asthana
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引用次数: 0

摘要

母细胞倍体是一种与急性淋巴细胞白血病(ALL)患者预后相关的独特细胞基因组特征。近四倍体(NT)(81 ~ 103条染色体)是ALL中非常罕见的倍体异常。在大约1%的儿童b细胞前体ALL (BCP-ALL)中观察到它。在T-ALL中,尤其是成人T-ALL,更是罕见的疾病。在现有文献中仅发现少数病例报告。与BCP-ALL相比,T-ALL缺乏具有独立预后价值的复发性遗传异常。虽然b细胞ALL合并NT与标准的细胞基因组风险相关,但NT在t细胞ALL中的预后结果尚未确定。这种实体的常规核型难以执行和解释。因此,建议核型结果应辅以荧光原位杂交。在此,我们提出一个成人T-ALL病例检测到NT核型,重点是预后意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A T-cell adult acute lymphoblastic leukemia harboring a rare near-tetraploid karyotype
Blast ploidy is a distinctive cytogenomic feature related to the prognostic outcome of acute lymphoblastic leukemia (ALL) patients. Near tetraploidy (NT) (81–103 chromosomes) is a very rare ploidy anomaly in (ALL). It is observed in approximately 1% of childhood B-cell precursor ALL (BCP-ALL). In T-ALL specifically in adult T-ALL, it is furthermore rare entity. Only few case reports are found in the existing literature. Compared to BCP-ALL, T-ALL lacks recurrent genetic anomalies with independent prognostic value. Although B-cell ALL associated with NT is related to a standard cytogenomic risk, the prognostic outcome of NT in T-cell ALL is yet to be determined. Conventional karyotyping of this entity is difficult to perform and interpret. Thus, it is recommended that karyotype results should be supplemented by fluorescence in situ hybridization. Herewith, we present an adult T-ALL case detected with NT karyotype with emphasis on prognostic significance.
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