Chou T, Wakabayashi M, Hayashi N, Arakawa M
Department of Medicine (II), Niigata Univ Medical School.
Rinsho Ketsueki. 1992 Sep;33(9):1263-7.
Forty-three-year-old man with schizophrenia, who had been diagnosed as chronic myelogenous leukemia (CML) and had been treated with hydroxyurea for 3 months, developed blastic crisis. The cytochemical study of the blastic cells showed POX (+), SBB (+) and TdT (+). The surface marker analysis revealed that the blastic cells expressed both myeloid (CD13, 33) and lymphoid (CD10, 19) markers. In the chromosomal analysis, additional chromosomal abnormality (11q+) was detected in all cells analysed (20/20) in addition to the standard type Ph1 chromosome. He was diagnosed as bi-phenotypic blastic crisis, and vincristine-prednisolone therapy was started. Initially, he responded to VP therapy well, but gradually became refractory to the therapy after 5 courses of VP. As many myeloblasts containing azurophilic granules were seen in the bone marrow after VP therapy, low dose Ara-C therapy was combined to VP. After 21 days of low dose Ara-C and VP, the percentage of the blast in the BM was significantly decreased and normal myeloid differentiation was observed after transient BM suppression. The chromosomal analysis showed the partial reappearance of standard Ph1 chromosome in 55% of the cells analyzed (11/20). Taken together, our data suggested that the combination of VP and low-dose Ara-C therapy might have some therapeutic benefit for the treatment of the CML with blastic crisis.
一名43岁患有精神分裂症的男性,此前被诊断为慢性粒细胞白血病(CML)并接受羟基脲治疗3个月后,发生了急变期。对原始细胞的细胞化学研究显示POX(+)、SBB(+)和TdT(+)。表面标志物分析表明,原始细胞同时表达髓系(CD13、33)和淋系(CD10、19)标志物。在染色体分析中,除了标准型Ph1染色体外,在所有分析的细胞(20/20)中均检测到额外的染色体异常(11q+)。他被诊断为双表型急变期,开始了长春新碱-泼尼松龙治疗。最初,他对VP治疗反应良好,但在5个疗程的VP治疗后逐渐对该治疗产生耐药。VP治疗后骨髓中可见许多含嗜天青颗粒的原始粒细胞,因此将小剂量阿糖胞苷治疗与VP联合使用。在小剂量阿糖胞苷和VP治疗21天后,骨髓中原始细胞百分比显著下降,在短暂的骨髓抑制后观察到正常的髓系分化。染色体分析显示,在55%的分析细胞(11/20)中标准Ph1染色体部分重现。综上所述,我们的数据表明,VP和小剂量阿糖胞苷联合治疗可能对慢性粒细胞白血病急变期的治疗有一定的治疗益处。