Wolf B C, Banks P M, Mann R B, Neiman R S
Department of Pathology, New England Deaconess Hospital, Boston, Massachusetts.
Am J Clin Pathol. 1988 Jan;89(1):69-75. doi: 10.1093/ajcp/89.1.69.
Spleens from 42 patients with polycythemia vera were studied with immunohistologic technics to assess the degree of hematopoietic cellularity in an attempt to clarify the pathogenesis of the splenomegaly characteristic of this disorder. The 22 spleens obtained in the erythrocytotic phase showed striking congestion with mature erythrocytes but no significant extramedullary hematopoiesis. However, the 20 spleens obtained in the spent phase showed prominent trilinear extramedullary hematopoiesis. Increasing splenomegaly with extramedullary hematopoiesis correlated with the development of increased medullary reticulin and peripheral blood leukoerythroblastosis. Splenic myeloid metaplasia is not a feature of uncomplicated polycythemia vera, and its presence indicates progression to the spent phase, or postpolycythemic myeloid metaplasia. The authors' findings indicate that the presence of hematopoietic precursors in the spleen in the spent phase of polycythemia vera and in agnogenic myeloid metaplasia is a result of their filtration from the peripheral blood.
对42例真性红细胞增多症患者的脾脏进行了免疫组织学技术研究,以评估造血细胞的程度,试图阐明该疾病特征性脾肿大的发病机制。在红细胞增多期获得的22个脾脏显示成熟红细胞明显充血,但无明显的髓外造血。然而,在终末期获得的20个脾脏显示出显著的三系髓外造血。脾肿大伴髓外造血增加与骨髓网硬蛋白增加和外周血幼稚粒-幼红细胞增多的发展相关。脾髓样化生不是单纯真性红细胞增多症的特征,其出现表明已进展至终末期或真性红细胞增多症后髓样化生。作者的研究结果表明,真性红细胞增多症终末期和特发性髓样化生患者脾脏中造血前体细胞的存在是它们从外周血滤过的结果。