Victorian Cancer Cytogenetics Service, St Vincent's Hospital Melbourne, Fitzroy, VIC 3065, Australia.
Biomed Res Int. 2013;2013:164501. doi: 10.1155/2013/164501. Epub 2013 Mar 28.
The diagnosis of acute promyelocytic leukaemia (APL) is usually confirmed by cytogenetics showing the characteristic t(15;17), but a minority of patients have a masked PML/RARA fusion. We report ten patients with APL and no evidence of the t(15;17), in whom the insertion of RARA into PML could not be demonstrated by initial FISH studies using a standard dual fusion probe but was readily identified using smaller probes. Given the need for rapid diagnosis of APL, it is important to be aware of the false negative rate for large PML/RARA FISH probes in the setting of masked rearrangements.
急性早幼粒细胞白血病(APL)的诊断通常通过细胞遗传学证实存在特征性的 t(15;17),但少数患者存在 PML/RARA 融合的隐匿性改变。我们报告了 10 例 APL 患者,其无 t(15;17)的证据,最初使用标准双融合探针的 FISH 研究未能显示 RARA 插入 PML,但使用较小的探针可轻易识别。鉴于需要快速诊断 APL,重要的是要意识到在隐匿性重排的情况下,大型 PML/RARA FISH 探针的假阴性率。