Lawler S D, O'Malley F, Lobb D S
Scand J Haematol. 1976 Jul;17(1):17-28. doi: 10.1111/j.1600-0609.1976.tb02836.x.
A cytogenetic study of Ph1 positive myeloid leukaemia in both chronic and acute phases had been made by a chromosome banding technique. The translocation (t(9;22)(q34;q11), designated t(Ph1) was present in the myeloid cells of 43 of 44 patients; the exceptional case had normal number 9 chromosomes and a different translocation (t(19;22)(q13;q11)). A translocation additional to that involving the Ph1 was found as a stable abnormality present in all myeloid cells in 4 patients, chromosome 17 being involved in 2. The association of isochromosome number 17 with blast crisis was confirmed. New data were obtained concerning the significance of duplicated or dicentric Ph1 chromosomes and their relationship with the 9q+ anomaly. Monoclonal origin of Ph1 was confirmed in cases with polymorphic number 22 or 9 chromosomes.
运用染色体显带技术对慢性期和急性期Ph1阳性髓系白血病进行了细胞遗传学研究。44例患者中有43例的髓系细胞存在易位(t(9;22)(q34;q11),命名为t(Ph1));例外的那例患者9号染色体数目正常,存在另一种不同的易位(t(19;22)(q13;q11))。在4例患者中发现除涉及Ph1的易位外,还存在一种稳定的额外易位异常,其中2例涉及17号染色体。证实了17号等臂染色体与急变期的关联。获得了关于重复或双着丝粒Ph1染色体的意义及其与9q+异常关系的新数据。在22号或9号染色体数目多态的病例中证实了Ph1的单克隆起源。