Janvier M, Tobelem G, Daniel M T, Bernheim A, Marty M, Boiron M
Scand J Haematol. 1984 Apr;32(4):385-90. doi: 10.1111/j.1600-0609.1984.tb00693.x.
Between 1978 and 1980, 45 cases of acute monoblastic leukaemia have been diagnosed, treated and followed in our institute. Morphological diagnosis was performed according to the French-American-British classification. Tumoral syndrome (particularly extra-medullary) and hyperleucocytosis were the most striking findings at the time of diagnosis. Cytogenetic analysis performed in 31 cases before treatment has showed that abnormality of the long arm of chromosome 11 seemed to be more frequently associated with the poorly differentiated cytological subtype M5 (a). Intensive chemotherapy with zorubicin and cytosine arabinoside led to complete remission in 75% of the cases. Central nervous system prophylaxis appeared definitively useful in preventing meningeal relapse. Despite a prolongation of the median duration of complete remission which now reaches 12 months, the prognostic is still poor.
1978年至1980年间,我院共诊断、治疗并随访了45例急性单核细胞白血病患者。形态学诊断依据法美英分类法进行。肿瘤综合征(尤其是髓外病变)和白细胞增多症是诊断时最显著的表现。对31例患者治疗前进行的细胞遗传学分析显示,11号染色体长臂异常似乎更常与细胞分化差的M5(a)细胞学亚型相关。采用柔红霉素和阿糖胞苷进行强化化疗,使75%的病例达到完全缓解。中枢神经系统预防措施对于预防脑膜复发显然有效。尽管完全缓解的中位持续时间延长至目前的12个月,但预后仍然很差。