Xue Y, Li J, Xia X
Jiangsu Institute of Hematology, First Affiliated Hospital, Suzhou Medical College.
Zhonghua Nei Ke Za Zhi. 1997 Mar;36(3):190-2.
To determine the chromosomal abnormalities and their clinical significance in adult acute lymphoblastic leukemia, karyotypic analyses with R- and/or G-banding were performed in 101 newly diagnosed ALL patients. The results showed that 69 (68.32%) cases had clonal chromosomal abnormalities and specific abnormalities including Philadelphia chromosome (32.67%), t(4;11) (2.97%), t(11;14) (3.96%), abnormalities of 8q24 (2.97%), 6q- (4.96%). Patients with Ph chromosome showed higher leukocyte counts and more frequent hepatosplenomegaly and most of them were L2 and B lineage subtypes. They had lower complete remission (CR) rate, needed longer time to achieve CR and relapsed earlier as compared with patients without Ph chromosome. These suggested that chromosomal abnormalities are very frequent and some specific abnormalities had specific clinical features.
为确定成人急性淋巴细胞白血病的染色体异常及其临床意义,对101例新诊断的急性淋巴细胞白血病患者进行了R显带和/或G显带核型分析。结果显示,69例(68.32%)患者存在克隆性染色体异常,包括费城染色体(32.67%)、t(4;11)(2.97%)、t(11;14)(3.96%)、8q24异常(2.97%)、6q-(4.96%)等特异性异常。有费城染色体的患者白细胞计数较高,肝脾肿大更为常见,且大多为L2和B系亚型。与无费城染色体的患者相比,他们的完全缓解(CR)率较低,达到CR所需时间更长,且复发更早。这些表明染色体异常非常常见,一些特异性异常具有特定的临床特征。