全反式维甲酸治疗急性早幼粒细胞白血病的染色体观察。

Hematologic pathology Pub Date : 1992-01-01
X Wu, W W Wang, Z L Zhou, G C Zhu, Z C Yang, J S Ying, Y Zhu
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引用次数: 0

摘要

8例急性早幼粒细胞白血病患者在全反式维甲酸诱导分化过程中观察到染色体变化。用Giemsa-R带法分析短期培养后患者骨髓标本的核型。分析显示,8例患者均有15 ~ 17号染色体异常易位,但经全反式维甲酸治疗后缓解期,特征性的t(15;17)染色体异常消失。然而,在3例患者中检测到的这种染色体畸变在RA诱导的早期持续存在,尽管患者仍然可以实现完全缓解。然而,发现异常核型的百分比在早期下降。这种现象可能是临床缓解的重要指标。1例复发时,t(15;17)再次出现。因此,t染色体(15;17)不仅有助于诊断,而且有助于观察急性早幼粒细胞白血病的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chromosome observations of acute promyelocytic leukemia treated with all-trans retinoic acid.

Chromosome changes were observed in 8 patients with acute promyelocytic leukemia during the all-trans retinoic acid-induced differentiation course. Karyotype of patient bone marrow specimens after short-term incubation were analyzed using Giemsa-R banding. Analyses showed all 8 patients had the abnormal translocation between chromosomes 15 and 17, but when those patients were treated with all-trans retinoic acid and were in remission, the characteristic t(15;17) chromosomal abnormality disappeared. However, this aberration of chromosomes detected in 3 patients persisted during the early period of RA induction, although the patients could still achieve complete remission. However, it was found that the percentage of abnormal karyotypes declined during this early period. This phenomenon may be an important indicator for clinical remission. When one case relapsed, the t(15;17) reappeared. Thus the chromosome t(15;17) was not only useful in diagnosis, but also helpful in observing prognosis in acute promyelocytic leukemia.

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