Akahoshi M, Oshimi K, Mizoguchi H, Okada M, Enomoto Y, Watanabe Y
Department of Medicine, Tokyo Women's Medical College, Japan.
Cancer. 1987 Dec 1;60(11):2654-61. doi: 10.1002/1097-0142(19871201)60:11<2654::aid-cncr2820601114>3.0.co;2-q.
Two cases of myeloproliferative disorders terminating in acute megakaryoblastic leukemia are reported. One case began as primary myelofibrosis and the other as chronic myelogenous leukemia. Blast cells in the acute leukemic phase were identified as megakaryoblasts by the presence of platelet peroxidase. The clinical course is described, and the morphology, immunologic studies, and ultrastructure studies of the blast cells are reported. On cytogenetic analysis both cases had a translocation involving the No. 3 chromosome locus q26.2. The present data suggest that 3q26 may be associated with transformation of the megakaryocytic lineage.
报告了两例以急性巨核细胞白血病告终的骨髓增殖性疾病病例。一例始于原发性骨髓纤维化,另一例始于慢性粒细胞白血病。急性白血病期的原始细胞因存在血小板过氧化物酶而被鉴定为巨核母细胞。描述了临床病程,并报告了原始细胞的形态学、免疫学研究和超微结构研究。细胞遗传学分析显示,两例均有涉及3号染色体位点q26.2的易位。目前的数据表明,3q26可能与巨核细胞系的转化有关。