Bainton D F, Friedlander L M, Shohet S B
Blood. 1977 May;49(5):693-704.
Granule formation was investigated in differentiating neutrophils of a patient with acute myelogenous leukemia (AML) by means of the combined techniques of electron microscopy and peroxidase cytochemistry. Two important pathologic features were observed: first, an abnormal concentration and packaging of peroxidase into Auer rods in leukemic promyelocytes, and second, the presence of Auer rods surrounded by single-unit membranes in some mature polymorphonuclear leukocytes (PMN). An additional unexpected finding was the discovery of two distinct populations of PMN circulating concurrently; a minor (less than 5%) normal one that contained both peroxidase-positive azurophilic and peroxidase-negative specific granules and a major abnormal one characterized by the absence of specific granules. None of these abnormalities was observed during the two remissions of this patient's disease. During relapse a "hiatus leukemicus" occurred, which also revealed two populations of cells, a majority population of leukemic blasts, and a minority population of a few normal PMN. These findings documented several developmental abnormalities in the differentiating cells of myelogenous leukemia and also suggested that concurrent normal and abnormal populations of PMN may be a helpful diagnostic feature of a leukemic process.
通过电子显微镜和过氧化物酶细胞化学的联合技术,对一名急性髓性白血病(AML)患者分化中的中性粒细胞的颗粒形成进行了研究。观察到两个重要的病理特征:第一,在白血病早幼粒细胞中,过氧化物酶异常浓缩并包装成Auer小体;第二,在一些成熟的多形核白细胞(PMN)中,Auer小体被单单位膜包围。另一个意外发现是同时发现了两种不同的循环PMN群体;一种少量(少于5%)的正常群体,含有过氧化物酶阳性的嗜天青颗粒和过氧化物酶阴性的特异性颗粒,另一种主要的异常群体,其特征是缺乏特异性颗粒。在该患者疾病的两次缓解期均未观察到这些异常。在复发期间出现了“白血病裂孔”,这也显示出两种细胞群体,大多数是白血病原始细胞群体,少数是一些正常的PMN。这些发现记录了髓性白血病分化细胞中的几种发育异常,也表明PMN的正常和异常群体同时存在可能是白血病过程的一个有用的诊断特征。