Ribeiro R C, Pui C H, Schell M J
Department of Hematology/Oncology, St. Jude Children's Research Hospital, Memphis, TN 38101.
Cancer. 1988 Feb 1;61(3):589-92. doi: 10.1002/1097-0142(19880201)61:3<589::aid-cncr2820610328>3.0.co;2-l.
Twenty-four (1.6%) of 1466 children with acute lymphoblastic leukemia (ALL) treated at St. Jude Children's Research Hospital had vertebral compression fractures at diagnosis. When compared with patients without this complication, they were more likely to have good prognostic features, including a leukocyte count of greater than 25 X 10(9)/l, a leukemic cell DNA index of greater than 1.15, and hyperdiploidy (greater than 50 chromosomes). Complete remission of ALL was induced in all patients, and symptoms of vertebral compression fractures abated following antileukemia therapy. Although the diagnosis of ALL was delayed for some patients because this unusual presenting complication was not recognized as such, their treatment outcome was as good as that for other children with "standard-risk" ALL.
在圣犹大儿童研究医院接受治疗的1466例急性淋巴细胞白血病(ALL)患儿中,有24例(1.6%)在诊断时发生了椎体压缩性骨折。与没有这种并发症的患者相比,他们更有可能具有良好的预后特征,包括白细胞计数大于25×10⁹/L、白血病细胞DNA指数大于1.15以及超二倍体(大于50条染色体)。所有患者的ALL均诱导完全缓解,抗白血病治疗后椎体压缩性骨折症状减轻。尽管由于这种不寻常的首发并发症未被识别,一些患者的ALL诊断有所延迟,但他们的治疗结果与其他“标准风险”ALL患儿的治疗结果一样好。