具有隐匿型PML-RARα融合基因的罕见急性早幼粒细胞白血病一例报告并文献复习
急性早幼粒细胞白血病(APL)是急性髓系白血病的一个特殊亚型,其特异性的细胞遗传学异常为t(15;17)(q22;q12),15号染色体上的PML基因和17号染色体上的维甲酸受体(RARα)基因融合,形成PML-RARα融合基因,其编码PML-RARα的蛋白,可以阻止细胞分化,从而导致骨髓中堆积大量的异常早幼粒细胞。...
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Published in | 中华血液学杂志 Vol. 37; no. 11; pp. 1001 - 1002 |
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Main Author | |
Format | Journal Article |
Language | Chinese |
Published |
100191,北京大学第三医院血液科
2016
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Subjects | |
Online Access | Get full text |
ISSN | 0253-2727 |
DOI | 10.3760/cma.j.issn.0253-2727.2016.11.016 |
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Abstract | 急性早幼粒细胞白血病(APL)是急性髓系白血病的一个特殊亚型,其特异性的细胞遗传学异常为t(15;17)(q22;q12),15号染色体上的PML基因和17号染色体上的维甲酸受体(RARα)基因融合,形成PML-RARα融合基因,其编码PML-RARα的蛋白,可以阻止细胞分化,从而导致骨髓中堆积大量的异常早幼粒细胞。 |
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AbstractList | 急性早幼粒细胞白血病(APL)是急性髓系白血病的一个特殊亚型,其特异性的细胞遗传学异常为t(15;17)(q22;q12),15号染色体上的PML基因和17号染色体上的维甲酸受体(RARα)基因融合,形成PML-RARα融合基因,其编码PML-RARα的蛋白,可以阻止细胞分化,从而导致骨髓中堆积大量的异常早幼粒细胞。 @@ |
Author | 王艳芳 刘佳 董菲 田磊 王晶 郤连永 克晓燕 |
AuthorAffiliation | 北京大学第三医院血液科,100191 |
AuthorAffiliation_xml | – name: 100191,北京大学第三医院血液科 |
Author_FL | Ke Xiaoyan Tian Lei Xi Lianyong Liu Jia Dong Fei Wang Yanfang Wang Jing |
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DocumentTitleAlternate | The study of one ease of APL with rare cryptic PML- RARα fusion gene and the literatures review |
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Notes | Wang Yan- fang, Liu Jia, Dong Fei, Tian Lei, Wang ,ling, Xi Lianyong, Ke Xiaoyan (Department of Hematology, Peking University Third Hospital, Beijing 100191, China.) 12-1090/R |
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Snippet | 急性早幼粒细胞白血病(APL)是急性髓系白血病的一个特殊亚型,其特异性的细胞遗传学异常为t(15;17)(q22;q12),15号染色体上的PML基因和17号染色体上的维甲酸受体(RARα)基因融合,形成PML-RARα融合基因,其编码PML-RARα的蛋白,可以阻止细胞分化,从而导致骨髓中堆积大量的异常早幼粒细胞。 @@ |
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SubjectTerms | 15号染色体 17号染色体 PML-RARα融合基因 急性早幼粒细胞白血病 急性髓系白血病 文献复习 细胞遗传学异常 隐匿型 |
Title | 具有隐匿型PML-RARα融合基因的罕见急性早幼粒细胞白血病一例报告并文献复习 |
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