Bain Barbara
St Mary's Hospital Campus of Imperial College, St Mary's Hospital, London, W2 1NY, Great Britain.
Exp Oncol. 2004 Sep;26(3):166-9.
For more than two decades the French-American-British (FAB) classification has provided a framework for the diagnosis and classification of the myelodysplastic syndromes. However, with widespread use of this classification, it became clear that prognostic differences existed within single categories. The FAB classification has therefore been modified by a World Health Organization (WHO) expert group to take account of these prognostic differences. In addition, therapy-related myelodysplasia and the 5q- syndrome have been recognized as distinct types of disorder and the existence of mixed myelodysplastic/myeloproliferative disorders has been recognized; chronic myelomonocytic leukaemia, previously regarded as one of the myelodysplastic syndromes, was re-assigned to this latter group of disorders.
二十多年来,法美英(FAB)分类为骨髓增生异常综合征的诊断和分类提供了一个框架。然而,随着该分类的广泛应用,很明显在单一类别中存在预后差异。因此,世界卫生组织(WHO)的一个专家组对FAB分类进行了修改,以考虑这些预后差异。此外,治疗相关的骨髓增生异常和5q-综合征已被确认为不同类型的疾病,并且混合性骨髓增生异常/骨髓增殖性疾病的存在也已得到认可;慢性粒单核细胞白血病,以前被视为骨髓增生异常综合征之一,被重新归类到后一组疾病中。