van Buchem M A, Hogendoorn P C, Levelt C N, van Hengel P, Colly L P, Kluin P M, Willemze R
Department of Hematology, University of Leiden, The Netherlands.
Leukemia. 1992 Feb;6(2):142-9.
The pathogenesis of pulmonary leukostasis in leukemia was studied in a rat model by investigating the course of its development. Leukemia was induced by inoculating rats with leukemic cells. The earliest stage of leukostasis was found from day 14 onward, when leukemic cells appeared in the peripheral blood, and was characterized by accumulation of leukemic cells at the capillary level. Simultaneous with the increase of leukemic cell concentrations in the peripheral blood, accumulation in capillaries increased gradually over a period of several days. This was accompanied by increasing severity of tachypnea. Shortly before death, aggregates consisting almost solely of leukemic cells were found in medium-sized blood vessels. This stage was rapidly followed by the end-stage, characterized by complete obstruction of the lung vasculature--including the largest arteries and veins--by leukemic cell aggregates, giving rise to extensive hemorrhages and edema. The end-stage was considered to be the cause of death, which occurred 18-26 days after the inoculation. The histological and ultrastructural findings in this study suggest that besides the size and stiffness of individual leukemic cells, interactions not only between leukemic cells, but also between leukemic cells and the endothelium play a role in the pathogenesis of pulmonary leukostasis.
通过研究肺白细胞淤滞症在大鼠模型中的发展过程,对白血病中肺白细胞淤滞症的发病机制进行了研究。通过给大鼠接种白血病细胞来诱发白血病。白细胞淤滞症的最早阶段从第14天开始出现,此时外周血中出现白血病细胞,其特征是白血病细胞在毛细血管水平积聚。随着外周血中白血病细胞浓度的增加,毛细血管中的积聚在几天内逐渐增加。这伴随着呼吸急促的严重程度增加。在死亡前不久,在中等大小的血管中发现了几乎完全由白血病细胞组成的聚集体。这个阶段之后迅速进入终末期,其特征是白血病细胞聚集体完全阻塞肺血管系统,包括最大的动脉和静脉,导致广泛的出血和水肿。终末期被认为是死亡原因,死亡发生在接种后18 - 26天。本研究中的组织学和超微结构结果表明,除了单个白血病细胞的大小和硬度外,白血病细胞之间以及白血病细胞与内皮细胞之间的相互作用在肺白细胞淤滞症的发病机制中起作用。