Benedict W F, Lange M, Greene J, Derencsenyi A, Alfi O S
Blood. 1979 Oct;54(4):818-23.
The chromosomal complement of 28 children with the diagnosis of acute nonlymphocytic leukemia (ANLL) were examined. An abnormal cytogenetic pattern was found in 50% of these patients, which is similar to the results in adults with ANLL. Unlike the reports in adult patients, however, no specific chromosomal changes were found. This observation may imply that the etiology and mechanisms by which abnormal clones develop in ANLL could differ significantly between children and adults. Those patients with chromosomal abnormalities in their initial bone marrow sample had a median survival of 7.1 mo, whereas those with a normal diploid pattern in their bone marrow had a median survival of 20.5 mo (1-sided, p = 0.04). If all metaphases were abnormal, the median survival was only 3 mo.
对28例诊断为急性非淋巴细胞白血病(ANLL)的儿童的染色体组进行了检查。在这些患者中,50%发现了异常的细胞遗传学模式,这与成人ANLL的结果相似。然而,与成人患者的报告不同,未发现特定的染色体变化。这一观察结果可能意味着,儿童和成人ANLL中异常克隆形成的病因和机制可能存在显著差异。初始骨髓样本中染色体异常的患者中位生存期为7.1个月,而骨髓中具有正常二倍体模式的患者中位生存期为20.5个月(单侧,p = 0.04)。如果所有中期细胞均异常,中位生存期仅为3个月。