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
Main Author 王艳芳 刘佳 董菲 田磊 王晶 郤连永 克晓燕
Format Journal Article
LanguageChinese
Published 100191,北京大学第三医院血液科 2016
Subjects
Online AccessGet full text
ISSN0253-2727
DOI10.3760/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。
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。
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Author 王艳芳 刘佳 董菲 田磊 王晶 郤连永 克晓燕
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Tian Lei
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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.)
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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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StartPage 1001
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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