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An acquired Robertsonian translocation in prolymphocytic leukemia: a case presentation and review.

作者信息

Morgan R, Sandberg A A, Jarzabek V, Scheerer P, Hecht F

出版信息

Cancer Genet Cytogenet. 1987 Apr;25(2):293-301. doi: 10.1016/0165-4608(87)90190-7.

DOI:10.1016/0165-4608(87)90190-7
PMID:3470118
Abstract

Robertsonian translocations between the acrocentric autosomes are the most common type of constitutional chromosome rearrangement in humans. However, Robertsonian translocations are very rarely acquired in cancer cells. We report a patient with prolymphocytic leukemia and an acquired Robertsonian translocation in the leukemic cells. The translocation was between chromosomes #13 and #15; t(13;15)(q11;p12). Two other cases of malignancy with an acquired Robertsonian translocation have been found, one being of the t(13;15) type, which accounts for only 1% of constitutional Robertsonian translocations. We propose, therefore, that although Robertsonian translocations are occasionally observed in cancer cells, they are very rarely acquired.

摘要

相似文献

1
An acquired Robertsonian translocation in prolymphocytic leukemia: a case presentation and review.
Cancer Genet Cytogenet. 1987 Apr;25(2):293-301. doi: 10.1016/0165-4608(87)90190-7.
2
Acquired Robertsonian translocations in two leukemia patients.两名白血病患者中获得性罗伯逊易位
Cancer Genet Cytogenet. 2001 Dec;131(2):104-8. doi: 10.1016/s0165-4608(01)00478-2.
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Prader-Willi syndrome and Robertsonian translocations involving chromosome 15.
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Acquired Robertsonian translocations are not rare events in acute leukemia and lymphoma.获得性罗伯逊易位在急性白血病和淋巴瘤中并非罕见事件。
Cancer Genet Cytogenet. 2004 May;151(1):14-35. doi: 10.1016/j.cancergencyto.2003.09.019.
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Robertsonian translocation as an acquired karyotypic abnormality in leukaemia.罗伯逊易位作为白血病中一种后天获得的核型异常。
Br J Haematol. 1997 Jul;98(1):213-5. doi: 10.1046/j.1365-2141.1997.1702992.x.
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Characterization of Robertsonian translocations by using fluorescence in situ hybridization.利用荧光原位杂交技术对罗伯逊易位进行特征分析。
Am J Hum Genet. 1992 Jan;50(1):174-81.
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Constitutional Robertsonian T(15;22) in Ph-positive CML.Ph 阳性慢性髓性白血病中的先天性罗伯逊易位 T(15;22)
Hum Genet. 1987 Aug;76(4):399. doi: 10.1007/BF00272453.
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t(9;22)(q34;q11.2) is a recurrent constitutional non-Robertsonian translocation and a rare cytogenetic mimic of chronic myeloid leukemia.t(9;22)(q34;q11.2)是一种常见的遗传性非罗伯逊易位,也是一种罕见的慢性髓性白血病细胞遗传学模拟。
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An acquired Robertsonian 13;15 translocation in acute myelogenous leukemia (M5b).急性髓系白血病(M5b)中一种获得性13;15罗伯逊易位。
Int J Hematol. 1994 Feb;59(2):131-5.
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Molecular cytogenetic evidence to characterize breakpoint regions in Robertsonian translocations.用于表征罗伯逊易位中断点区域的分子细胞遗传学证据。
Cytogenet Cell Genet. 1990;54(3-4):97-102. doi: 10.1159/000132970.

引用本文的文献

1
Case report: CD8 positive T-cell Prolymphocytic Leukemia presenting complex karyotype with a rare chromosomal abnormality der(2)t(1;2)(q21;q37) and additional signals of the genes MYC, IGH, and TP53.病例报告:CD8 阳性 T 细胞原淋巴细胞白血病呈现复杂核型,伴有罕见的染色体异常 der(2)t(1;2)(q21;q37)以及 MYC、IGH 和 TP53 基因的额外信号。
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