Nowell P, Jensen J, Gardner F, Murphy S, Chaganti R S, German J
Cancer. 1976 Nov;38(5):1873-81. doi: 10.1002/1097-0142(197611)38:5<1873::aid-cncr2820380502>3.0.co;2-i.
Cytogenetic studies were done on 18 patients with myelofibrosis or the closely related syndrome, undifferentiated myeloproliferative disorder (MPD). Clones of cells with chromosome abnormalities were demonstrated in the blood of eight individuals, including two with a history of radiation therapy and two with "acute myelofibrosis". Trisomy 8 was present in the latter two patients, but otherwise, there was no consistent cytogenetic pattern or correlation with specific hematologic findings. Sixteen of these patients have been followed for more than 1 year or until death; none has progressed to leukemia. The results indicate that chromosome abnormalities are relatively common in this disorder, but as with polycythemia vera, and unlike some other "preleukemic" states, the aberrant clones in myelofibrosis do not appear to indicate that clinical leukemia is imminent.
对18例骨髓纤维化患者或与之密切相关的综合征——未分化骨髓增殖性疾病(MPD)患者进行了细胞遗传学研究。在8名个体的血液中发现了具有染色体异常的细胞克隆,其中包括2名有放射治疗史的患者和2名“急性骨髓纤维化”患者。后两名患者存在8号染色体三体,但除此之外,没有一致的细胞遗传学模式,也与特定的血液学发现无关。这些患者中有16例已随访1年以上或直至死亡;无一例进展为白血病。结果表明,染色体异常在这种疾病中相对常见,但与真性红细胞增多症一样,与其他一些“白血病前期”状态不同,骨髓纤维化中的异常克隆似乎并不表明临床白血病即将发生。