Linman J W, Bagby G C
Cancer. 1978 Aug;42(2 Suppl):854-64. doi: 10.1002/1097-0142(197808)42:2+<854::aid-cncr2820420707>3.0.co;2-w.
Retrospective analysis of patients with acute myelomonoblastic (or nonlymphocytic) leukemia has helped to clarify the early stages of the evolution of this disease, and a clinical picture has emerged that is sufficiently discriminating to permit prospective observations. The clinical and laboratory features of the hematologic disorder preceding overt, blast-cell leukemia (i.e., the "preleukemic syndrome" or "hemopoietic dysplasia") are described, and diagnostic criteria and approaches to management are considered. This hematologic syndrome appears to be a stage in a multiphasic panmyelopathy that involves all products of the marrow stem cell. Available data indicate that most of these patients develop acute leukemia within 24 months of the onset of the hematologic abnormalities, but longer courses are not uncommon. Prospective documentation in a large group of patients is needed before the natural course can be accurately defined; such studies are now being planned.
对急性粒单核细胞(或非淋巴细胞)白血病患者的回顾性分析有助于阐明该疾病演变的早期阶段,并且已经出现了一种具有足够鉴别力的临床表现,从而能够进行前瞻性观察。本文描述了明显的原始细胞白血病之前血液系统疾病的临床和实验室特征(即“白血病前期综合征”或“造血发育异常”),并考虑了诊断标准和治疗方法。这种血液系统综合征似乎是一种多相性全骨髓病的一个阶段,涉及骨髓干细胞的所有产物。现有数据表明,这些患者中的大多数在血液学异常出现后的24个月内会发展为急性白血病,但病程较长的情况也并不罕见。在能够准确界定其自然病程之前,需要在一大群患者中进行前瞻性记录;此类研究目前正在规划中。