Biemer J J
Ann Clin Lab Sci. 1983 Mar-Apr;13(2):156-62.
While the preleukemic syndrome (PLS) is not a homogeneous entity, its spectrum of clinical and laboratory findings has been sufficiently characterized to allow increasing certainty in its recognition. Approximately 25 percent of these patients can be expected to develop overt acute nonlymphocytic leukemia (ANLL) within an average of two to three years, and another 40 percent will die of non-leukemic complications usually related to their cytopenias within a similar time period. The remaining patients may be stable and survive for prolonged periods. Accumulating evidence indicates that in the PLS, a stem cell neoplastic clonal proliferation has already been established and may frequently be demonstrated by cytogenic analysis or culture of marrow hematopoietic cells.
虽然白血病前期综合征(PLS)并非一个同质的实体,但其临床和实验室检查结果的范围已得到充分描述,从而在识别方面的确定性不断提高。预计这些患者中约25%会在平均两到三年内发展为明显的急性非淋巴细胞白血病(ANLL),另外40%会在类似时间段内死于通常与其血细胞减少相关的非白血病并发症。其余患者可能病情稳定并长期存活。越来越多的证据表明,在PLS中,干细胞肿瘤性克隆增殖已经确立,并且常常可以通过细胞遗传学分析或骨髓造血细胞培养来证实。