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隐匿性t(15;17)急性早幼粒细胞白血病伴PML-RARα融合基因插入4q21。

Masked t(15;17) APL with the insertion of PML-RARalpha fusion gene in 4q21.

作者信息

Haraguchi Kouichi, Ohno Nobuhito, Tokunaga Masahito, Tokunaga Mayumi, Itoyama Takahiro, Gotoh Minako, Taniwaki Masafumi, Tubouchi Hirohito

机构信息

Department of Digestive and Life-style Related Diseases, Human Environmental Sciences, Health Research Studies, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8520, Japan.

出版信息

Leuk Res. 2009 Nov;33(11):1552-5. doi: 10.1016/j.leukres.2009.04.033. Epub 2009 May 27.

Abstract

Most cases of acute promyelocytic leukemia (APL) are characterized by the reciprocal translocation t(15;17); however, several complex variant translocations have also been reported. Here we report complex cytogenetic abnormalities without t(15;17) assayed by the G-banding method in a 62-year-old woman with the typical morphology and clinical features of APL. Based on spectral karyotyping and FISH analyses, we confirm the insertion of a cryptic chromosomal segment containing the PML/RARalpha fusion gene. The patient achieved complete remission after treatment with all-trans retinoic acid (ATRA) alone. Although the mechanism of this cryptic variant insertion is not known, we conclude that the insertion of PML-RARalpha fusion into 4q21 seems not to alter the effectiveness of treatment with ATRA.

摘要

大多数急性早幼粒细胞白血病(APL)病例的特征是相互易位t(15;17);然而,也有一些复杂的变异易位报道。在此,我们报告1例62岁具有典型APL形态学和临床特征的女性患者,经G显带法检测,存在无t(15;17)的复杂细胞遗传学异常。基于光谱核型分析和荧光原位杂交(FISH)分析,我们证实了一个含有PML/RARα融合基因的隐匿性染色体片段的插入。该患者单独使用全反式维甲酸(ATRA)治疗后获得完全缓解。虽然这种隐匿性变异插入的机制尚不清楚,但我们得出结论,PML-RARα融合插入到4q21似乎并不改变ATRA治疗的有效性。

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