Breatnach F, Chessells J M, Greaves M F
Br J Haematol. 1981 Nov;49(3):387-93. doi: 10.1111/j.1365-2141.1981.tb07241.x.
Transient pancytopenia preceded the onset of acute leukaemia in eight of 360 (2%) of children with acute lymphoblastic leukaemia (ALL) but did not occur in 70 cases of acute non-lymphoblastic leukaemia. The patients developed overt leukaemia within 5-38 weeks of first presentation with features of marrow failure. Immunological classification of blast cells was performed in six of the eight patients and all had phenotype of common-ALL (c-ALL). We conclude that the sydnrome of pre-leukaemia aplasia in childhood is a feature of c-ALL.
在360例急性淋巴细胞白血病(ALL)患儿中,有8例(2%)在急性白血病发作前出现短暂全血细胞减少,但70例急性非淋巴细胞白血病患儿未出现这种情况。这些患者在首次出现骨髓衰竭特征后的5 - 38周内发展为明显的白血病。对8例患者中的6例进行了原始细胞的免疫分类,所有患者均具有普通ALL(c-ALL)的表型。我们得出结论,儿童白血病前期再生障碍性贫血综合征是c-ALL的一个特征。