Fitzgerald P H, Morris C M, Giles L M
Hum Genet. 1982;60(3):281-3. doi: 10.1007/BF00303020.
The 24-h culture of bone marrow from patients with acute myeloblastic leukemia (AML) and acute promyelocytic leukemia (APL) gave more analyzable metaphase cells and improved chromosome morphology compared with direct preparations. Culture increased the proportion of cytogenetically abnormal cells, and in six bone marrows were the direct preparation failed, a result was obtained from the cultured preparation. The culture of bone marrow from patients with APL led to the detection of clones carrying the t(15;17) that were not found in direct preparations. Such sequestered clones were not found in AML and acute myelomonocytic leukemia (AMMoL). Cultured preparations were no better than direct preparations from AMMoL.
与直接制片相比,急性髓细胞白血病(AML)和急性早幼粒细胞白血病(APL)患者骨髓的24小时培养产生了更多可分析的中期细胞,并改善了染色体形态。培养增加了细胞遗传学异常细胞的比例,在6例直接制片失败的骨髓中,培养制片获得了结果。APL患者骨髓培养导致检测到直接制片中未发现的携带t(15;17)的克隆。AML和急性粒单核细胞白血病(AMMoL)中未发现此类隐匿克隆。AMMoL的培养制片并不比直接制片好。