Reiffers J, Dachary D, David B, Bernard P, Marit G, Boisseau M, Broustet A
Acta Haematol. 1985;73(4):228-31. doi: 10.1159/000206334.
The progression of primary thrombocythemia (PT) into acute leukemia was diagnosed in a 64-year-old man who was previously treated by hydroxyurea without alkylating agents or radioactive phosphorus. Such an event has only been reported in very rare cases. The blast cells had a lymphocytic morphology but were identified as promegakaryoblasts by the ultrastructural demonstration of platelet peroxidase. These data suggest that a megakaryoblastic transformation could occur in PT as had previously been reported in chronic granulocytic leukemia.
一名64岁男性被诊断为原发性血小板增多症(PT)进展为急性白血病,该患者此前接受过羟基脲治疗,未使用烷化剂或放射性磷。这种情况仅在极少数病例中有报道。原始细胞具有淋巴细胞形态,但通过血小板过氧化物酶的超微结构证明被鉴定为原巨核细胞。这些数据表明,PT可能会发生巨核细胞转化,正如先前在慢性粒细胞白血病中所报道的那样。