髓系白血病
川地34
基因复制
串联外显子复制
血液病理学
生物
白血病
髓样
核型
病理
免疫学
细胞遗传学
医学
基因
干细胞
遗传学
染色体
作者
Steven J. Kussick,Derek L. Stirewalt,Hye-Son Yi,Kayla M. Sheets,Era L. Pogosova‐Agadjanyan,Scott Braswell,Thomas H. Norwood,Jerald P. Radich,Brent L. Wood
出处
期刊:Leukemia
[Springer Nature]
日期:2004-09-02
卷期号:18 (10): 1591-1598
被引量:87
标识
DOI:10.1038/sj.leu.2403458
摘要
In a 5-year survey of nonpromyelocytic/nonmonocytic acute myeloid leukemias (AMLs) diagnosed in the University of Washington Hematopathology Laboratory, we identified 19 cases containing distinctive, cup-like nuclear indentation in 10% or more of the blasts ('AML-cuplike'). Fourteen of these cases (74%) demonstrated near-complete loss of HLA-DR expression, while the other five cases showed partial loss of HLA-DR. A total of 16 of the cases (84%) demonstrated internal tandem duplication (ITD) of the Flt3 gene. When compared to a selected set of AMLs lacking this nuclear morphology, AML-cuplike was significantly more likely to lack HLA-DR and CD34 expression, to express CD123 without CD133, to have a normal karyotype, and to harbor the Flt3 ITD. To characterize AML-cuplike in an unselected series of AMLs, we analyzed 42 consecutive nonpromyelocytic/nonmonocytic AMLs diagnosed in our laboratory during a 6-month period in 2002. Strikingly, in this unselected series, there was a statistically significant coincidence of invaginated nuclear morphology, loss of HLA-DR, and presence of the Flt3 ITD beyond that expected if these three features were unrelated, suggesting that AMLs with these three features may represent a distinct AML subset.
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