Acute myeloid leukemia with a late-appearing Philadelphia chromosome:a case report and literature review
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摘要: 费城染色体由9号和22号染色体易位形成特征性Ph染色体和具有酪氨酸激酶活性的BCR-ABL融合蛋白,是慢性粒细胞白血病的重要细胞遗传学标志。此外,Ph染色体也常见于高危急性淋巴细胞白血病。急性髓系白血病(acute myeloid leukemia,AML)患者出现Ph染色体临床上十分罕见,检出率仅约0.5%~3.0%[1-3]。Ph阳性AML发生率较低,缓解率低,预后差。Ph阴性AML复发为Ph阳性AML极为罕见,国内尚未发现相关报道
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关键词:
- 急性髓系白血病 /
- 费城染色体 /
- BCR-ABL融合基因 /
- 复发
Abstract: To improve the understanding and experience of the rare disease of Philadelphia chromosome appearing during recurrence of Ph-negative acute myeloid leukemia(AML),a case of 66-year-old male AML-M5 patient achieved complete remission after induction by DA regimen,but relapsed after 5 cycles of consolidation chemotherapy was studied.Chromosomal analysis showed the appearance of a Philadelphia chromosome and FISH studies revealed the BCR-ABL rearrangement.Imatinib was given orally,combined with lenalidomide,human recombinant interferon alpha-1 b and interleukin-2.The patient died of pulmonary infection.Late-appearing Philadelphia chromosome was associated with poor prognosis,playing a role in clonal evolution and disease progression.Tyrosine kinase inhibitors could benefit patients as a salvage treatment for AML with a late-appearing Philadelphia chromosome.-
Key words:
- acute myeloid leukemia /
- Philadelphia chromosome /
- BCR-ABL fusion gene /
- relapse
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