van Wering E R, Kamps W A, Vossen J M, van der List-Nuver C J, Theunissen P M
Br J Haematol. 1985 May;60(1):137-42. doi: 10.1111/j.1365-2141.1985.tb07394.x.
Three children with myelodysplastic syndromes (MDS) are described following the diagnostic criteria proposed by the FAB-cooperative group. Two of the children were of Turkish origin. Two cases fit the criteria for 'refractory anaemia with excess of blasts in transformation'. The other one is most consistent with 'chronic myelomonocytic leukaemia'. The patients received 'ANLL type' induction. One died during induction, two were grafted, of whom one survives.
按照法国-美国-英国（FAB）协作组提出的诊断标准，描述了3例骨髓增生异常综合征（MDS）患儿。其中2名患儿来自土耳其。2例符合“转化型伴原始细胞增多的难治性贫血”标准。另一例最符合“慢性粒-单核细胞白血病”。患者接受了“急性非淋巴细胞白血病（ANLL）型”诱导治疗。1例在诱导治疗期间死亡，2例接受了移植，其中1例存活。
