Fabich D R, Raich P C
Am J Clin Pathol. 1977 Apr;67(4):334-8. doi: 10.1093/ajcp/67.4.334.
This report describes three cases of an atypical variant of agnogenic myeloid metaplasia characterized by pancytopenia, high peripheral blast cell count, lack of significant splenomegaly or tear-drop poikilocytosis, and diffuse marrow fibrosis with an abnormal proliferation of megakaryocytes. It is suggested that these cases represent an acute variant of agnogenic myeloid metaplasia that is distinct from either the terminal blastic transformation of myelofibrosis or acute granulocytic leukemia.
本报告描述了三例原发性骨髓化生的非典型变异型病例,其特征为全血细胞减少、外周血原始细胞计数高、无明显脾肿大或泪滴状异形红细胞增多,以及伴有巨核细胞异常增殖的弥漫性骨髓纤维化。提示这些病例代表原发性骨髓化生的一种急性变异型,有别于骨髓纤维化的终末期原始细胞转化或急性粒细胞白血病。