Kass L
CRC Crit Rev Clin Lab Sci. 1979;10(4):329-96. doi: 10.3109/10408367909147138.
Preleukemic disorders are a controversial group of panmyelopathic disturbances that often precede the emergence of acute myeloblastic or myelomonocytic leukemia. In most instances, these preleukemic disorders are characterized by slowly developing myeloblastosis of the bone marrow. They include preleukemia, primary acquired panmyelopathy with myeloblastosis or smouldering acute leukemia, erythroleukemia, and subacute myelomonocytic leukemia. Sometimes, transitions between these various preleukemic disorders may be observed in a single individual. Abnormalities in cellular differentiation are expressed in cytochemical aberrations and in elaboration of colony forming units by marrow cells of patients with preleukemic disorders. Cytogenic and cellular kinetic abnormalities link preleukemic disorders closely to acute myeloblastic or myelomonocytic leukemia, although in many patients with preleukemic disorders, conversion to acute leukemia is not observed or perhaps not recognized. Understanding pathogenetic and pathophysiological aspects of preleukemic disorders may shed light on aspects of cellular proliferation and cellular differentiation in the acute leukemias.
白血病前期疾病是一组有争议的全骨髓病性紊乱,常先于急性髓细胞性白血病或粒单核细胞白血病出现。在大多数情况下,这些白血病前期疾病的特征是骨髓成髓细胞增多缓慢发展。它们包括白血病前期、伴有成髓细胞增多的原发性获得性全骨髓病或隐匿性急性白血病、红白血病和亚急性粒单核细胞白血病。有时,在同一个体中可观察到这些不同白血病前期疾病之间的转变。细胞分化异常表现为细胞化学异常以及白血病前期疾病患者骨髓细胞集落形成单位的生成。细胞遗传学和细胞动力学异常将白血病前期疾病与急性髓细胞性白血病或粒单核细胞白血病紧密联系起来,尽管在许多白血病前期疾病患者中,未观察到或可能未认识到其转化为急性白血病。了解白血病前期疾病的发病机制和病理生理学方面可能有助于阐明急性白血病中细胞增殖和细胞分化的相关方面。