Alter B P, Scalise A, McCombs J, Najfeld V
Polly Annenberg Levee Hematology Center, Mount Sinai School of Medicine, New York, N.Y.
Br J Haematol. 1993 Nov;85(3):627-30. doi: 10.1111/j.1365-2141.1993.tb03362.x.
Patients with Fanconi's anaemia (FA) have aplastic anaemia, leukaemia, myelodysplasia and tumours. Since leukaemia has a very poor prognosis, it is desirable to identify high-risk patients. To determine the significance of clonal marrow chromosomal abnormalities we began a prospective study in 17 patients: five were normal, eight aplastic, and four myelodysplastic. Three of 11 with adequate cytogenetics had transient abnormal clones. None had leukaemia at 3-24 months. Changing cytogenetic patterns may not be related to leukaemic evolution in patients with a DNA repair defect.
范科尼贫血(FA)患者会出现再生障碍性贫血、白血病、骨髓发育异常和肿瘤。由于白血病的预后很差,因此识别高危患者很有必要。为了确定克隆性骨髓染色体异常的意义,我们对17例患者开展了一项前瞻性研究:5例正常,8例再生障碍性贫血,4例骨髓发育异常。11例具备充分细胞遗传学资料的患者中有3例出现短暂异常克隆。在3至24个月时均未发生白血病。细胞遗传学模式的改变可能与DNA修复缺陷患者的白血病演变无关。