Oyarzo Mauricio P, Lin Pei, Glassman Armand, Bueso-Ramos Carlos E, Luthra Rajyalakshmi, Medeiros L Jeffrey
Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Am J Clin Pathol. 2004 Sep;122(3):348-58. doi: 10.1309/5DGB-59KQ-A527-PD47.
We report 12 cases of t(6;9)(p23;q34)-positive acute myeloid leukemia (AML), all classified using the criteria of the World Health Organization classification. There were 10 women and 2 men with a median age of 51 years (range, 20-76 years). Dysplasia was present in all cases (9 previously untreated), and basophilia was present in 6 (50%). Immunophenotypic studies showed that the blasts were positive for CD9, CD13, CD33, CD38, CD117, and HLA-DR in all cases assessed. CD34 was positive in 11 (92%) of 12, and terminal deoxynucleotidyl transferase was positive in 7 (64%) of 11 cases. The t(6;9) was the only cytogenetic abnormality detected in 7 cases (58%), and 5 cases had additional chromosomal abnormalities. Of 8 cases assessed, 7 (88%) had flt3 gene mutations. We conclude that t(6;9)-positive AML cases have distinctive morphologic features, an immunophenotype suggesting origin from an early hematopoietic progenitor cell, and a high frequency of flt3 gene mutations.
我们报告了12例t(6;9)(p23;q34)阳性的急性髓系白血病(AML)病例,所有病例均按照世界卫生组织分类标准进行分类。其中有10名女性和2名男性,中位年龄为51岁(范围20 - 76岁)。所有病例均存在发育异常(9例为初治患者),6例(50%)存在嗜碱性粒细胞增多。免疫表型研究显示,在所有评估病例中,原始细胞CD9、CD13、CD33、CD38、CD117和HLA - DR均呈阳性。12例中有11例(92%)CD34呈阳性,11例中有7例(64%)末端脱氧核苷酸转移酶呈阳性。7例(58%)仅检测到t(6;9)这一种细胞遗传学异常,5例存在其他染色体异常。在8例评估病例中,7例(88%)存在flt3基因突变。我们得出结论,t(6;9)阳性的AML病例具有独特的形态学特征、提示起源于早期造血祖细胞的免疫表型以及高频率的flt3基因突变。