Wang Huan-You, Ding Jiantao, Vasef Mohammad A, Wilson Kathleen S
Department of Pathology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75390, USA.
Am J Clin Pathol. 2009 Jan;131(1):64-71. doi: 10.1309/AJCPE0L7CIJZBIFR.
Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia. Submicroscopic insertion of RARalpha into PML, resulting in PML-RARalpha from derivative chromosome 15, has been rarely reported. Herein, we describe a functional PML-RARalpha transcript from the long arm of derivative chromosome 17 in a patient with microgranular APL. The conventional karyotype showed normal chromosomes 15 and 17. It is interesting that interphase and metaphase fluorescence in situ hybridizations demonstrated a fusion signal on the long arm of one chromosome 17 homolog, with both PML and RARalpha still present on chromosomes 15 and 17, respectively, although the signal on one chromosome 15 was weaker, indicating partial loss of the PML gene. Reverse transcriptase-polymerase chain reaction revealed a transcript corresponding to a break cluster region 3 (bcr3) short form PML-RARalpha. To the best of our knowledge, this is the first report of an APL with a bcr3/short form PML-RARalpha transcript generated from derivative chromosome 17 due to submicroscopic insertion of the PML gene into the RARalpha locus.
急性早幼粒细胞白血病(APL)是急性髓系白血病的一种亚型。RARα亚显微插入PML,导致衍生染色体15产生PML-RARα,这种情况鲜有报道。在此,我们描述了1例微颗粒型APL患者衍生染色体17长臂上功能性PML-RARα转录本。常规核型显示15号和17号染色体正常。有趣的是,间期和中期荧光原位杂交显示一条17号染色体同源染色体长臂上有融合信号,PML和RARα仍分别存在于15号和17号染色体上,尽管一条15号染色体上的信号较弱,提示PML基因部分缺失。逆转录聚合酶链反应显示有一个与断裂簇区域3(bcr3)短型PML-RARα相对应的转录本。据我们所知,这是首例因PML基因亚显微插入RARα基因座而由衍生染色体17产生bcr3/短型PML-RARα转录本的APL报告。