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一名17个月大的混合谱系白血病患儿中的“跳跃易位”

"Jumping translocation" in a 17-month-old child with mixed-lineage leukemia.

作者信息

Ben-Neriah S, Abramov A, Lerer I, Polliack A, Leizerowitz R, Rabinowitz R, Abeliovich D

机构信息

Department of Human Genetics, Hadassah University Hospital, Jerusalem, Israel.

出版信息

Cancer Genet Cytogenet. 1991 Oct 15;56(2):223-9. doi: 10.1016/0165-4608(91)90174-s.

Abstract

A 17-month-old child with acute biphenotypic (pre B-ALL/myelomonocytic) leukemia is reported. Extensive cytogenetic analysis performed at various stages of the disease revealed a clonal evolution at the time of initial diagnosis with two types of abnormal clones, one with trisomy 22 and two other related clones with trisomy 22 plus partial trisomy of the long arm of chromosome 1 associated with the telomeric segment of either chromosome 20q or 21p. At the time of relapse the only abnormal clone involved trisomy 22 and partial trisomy of 1q, but this time in association with the telomeric segment of 14p. The unique feature of these translocations is discussed and the possibility of the correlation between the different chromosomal abnormalities and the expression of biphenotypic markers is raised.

摘要

报告了一名17个月大患有急性双表型(前体B淋巴细胞白血病/骨髓单核细胞白血病)白血病的儿童。在疾病的各个阶段进行的广泛细胞遗传学分析显示,初始诊断时存在克隆进化,有两种异常克隆类型,一种是22号染色体三体,另外两种相关克隆是22号染色体三体加上1号染色体长臂的部分三体,与20号染色体长臂或21号染色体短臂的端粒片段相关。复发时唯一的异常克隆涉及22号染色体三体和1号染色体长臂部分三体,但这次与14号染色体短臂的端粒片段相关。讨论了这些易位的独特特征,并提出了不同染色体异常与双表型标志物表达之间相关性的可能性。

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