Slørdahl S H, Smeland E B, Holte H, Grønn M, Lie S O, Seip M
Department of Pediatrics, National Hospital, University of Oslo, Norway.
Med Pediatr Oncol. 1993;21(4):254-8. doi: 10.1002/mpo.2950210404.
Among 16 patients with Down's syndrome (DS) and acute leukemia admitted to our department during a ten year period, 6 were diagnosed as acute megakaryoblastic leukemia (AMkL). The diagnosis was based on clinical and hematologic criteria, confirmed in three patients with the use of monoclonal antibodies (MoAb) specific for megakaryocytic antigens. In these three, and in a fourth patient, the leukemic blasts were positive for other myeloid, lymphoid and erythroid markers in MoAb testing. We suggest that AMkL in DS is a mixed lineage leukemia with blasts presenting a variety of cell surface antigens, indicating origin from an early progenitor cell with the capability of megakaryocytic differentiation. Of the 6 patients with AMkL, 4 treated with standard AML protocols are in complete continuing remission (CCR) with observation periods from 57+ to 148+ months.
在十年期间入住我科的16例唐氏综合征(DS)合并急性白血病患者中,6例被诊断为急性巨核细胞白血病(AMkL)。诊断基于临床和血液学标准,3例患者通过使用针对巨核细胞抗原的单克隆抗体(MoAb)得以确诊。在这3例患者以及第4例患者中,白血病原始细胞在MoAb检测中对其他髓系、淋巴系和红系标志物呈阳性。我们认为,DS中的AMkL是一种混合谱系白血病,其原始细胞呈现多种细胞表面抗原,表明起源于具有巨核细胞分化能力的早期祖细胞。6例AMkL患者中,4例接受标准AML方案治疗,处于持续完全缓解(CCR)状态,观察期从57 +至148 +个月。