伊朗急性淋巴母细胞和髓性白血病患者的数字染色体异常

A. Malekasgar, M. Pedram, Sayyed kamal Eshagh housaini
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引用次数: 1

摘要

大多数ALL病例表现为染色体数目或结构改变的异常核型。儿童急性淋巴细胞白血病的染色体数目异常定义了不同的生物学亚群,对治疗的反应不同。试管用三种不同的方法培养,以便在一种方法失败时节省时间。然后收获培养物,固定细胞,准备染色体扩散。25例患者中,1例为伪二倍体核型,3例为四倍体核型,4例为低次二倍体核型,4例为高超二倍体核型,5例为低超d二倍体核型,8例为正常核型。其他一些因素,如年龄、性别、血亲、血红蛋白、白细胞计数和白血病细胞类型也进行了评估。我们发现有大量的患者具有次二倍体核型,但对治疗方案的反应仍然令人满意。通过4种不同培养方法的比较,我们发现直接培养法对倍性分析更有效。
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Numerical Chromosomal Abnormalities in Patients with Acute Lymphoblastic and Myeloid Leukemia in Iran
The majority of cases of ALL demonstrate an abnormal karyotype, either in chro mosome nu mber or structural changes. Abnormal chro mosome number in childhood acute lymphoblastic leukemia defines distinct biological subgroups with a different response to treatment. The tubes are cultured with three different protocols to save time if one protocol failed. Cultures are then harvested, and cells are fixed and chromosome spreads are prepared. Of 25 patient studied, one patient had psudodiploid karyotype, three patients had tetra-ploid karyotype, four patients had low hypo-diploid karyotype, four patients had high hyper-diploid karyotype, five patients had low hyper-d iploid karyotype and eight patients had normal karyotype. Some other factors like, Age, Sex, Consanguinity, Hemoglob in, W BC count, and Type of the leukemia cell also have been evaluated. We found excess number of patients having hypodiploid karyotype but still response to treatment protocols were satisfactory. By co mparison between 4 different cultures methods, we find d irect method to be more efficient for ploidy analysis.
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