净现值1
免疫分型
急性早幼粒细胞白血病
CD33
髓系白血病
髓样
CEBPA公司
白血病
医学
癌症研究
基因突变
病理
免疫学
川地34
生物
突变
流式细胞术
核型
基因
遗传学
干细胞
维甲酸
染色体
作者
Manuel J. Arana Rosainz,Nghia D. Nguyen,Amer Wahed,Laura Lelenwa,Fnu Aakash,K Schaefer,Adan Rios,Zeyad Kanaan,Lei Chen
摘要
Our findings provide additional evidence of association between NPM1-mutated AML with TET2 or IDH2 co-mutations and the APL-like immunophenotype. This AML subset was found to exist in both de novo and secondary AML. High WBC count and blasts with low to moderate side scatter and significant expression of CD4 are observed features that could assist in the differential diagnosis with APL. The occurrence of significant elevated D-dimer levels, or even overt DIC observed at diagnosis in these cases could be relevant for this AML subtype.
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