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原发性骨髓增生异常综合征患者染色体核型与IPSS 危度分组:FAB与WHO分型比较
引用本文:于明华,刘世和,邵英起,郝玉书,肖志坚. 原发性骨髓增生异常综合征患者染色体核型与IPSS 危度分组:FAB与WHO分型比较[J]. 中华血液学杂志, 2004, 25(8): 482-485
作者姓名:于明华  刘世和  邵英起  郝玉书  肖志坚
作者单位:300020,天津,中国医学科学院、中国协和医科大学血液学研究所、血液病医院实验血液学国家重点实验室
基金项目:国家自然科学基金资助项目 ( 3 0 2 70 5 73 )
摘    要:
目的 比较原发性骨髓增生异常综合征 (pMDS)患者WHO(2 0 0 1)分型和FAB分型的亚型与细胞遗传学异常及预后的相关性。方法 按FAB标准确诊并进行了染色体核型分析的 2 37例pMDS患者 ,重新进行血片和骨髓片分类计数并按WHO标准进行分型 ,对两种分型结果的染色体核型异常和国际预后积分系统 (IPSS)危度分组与各亚型的关系进行比较。结果 按FAB标准分型各亚型的染色体异常检出率及染色体异常危度分组无显著性差异 ,按WHO标准分型的难治性血细胞减少伴多系发育异常 (RCMD)患者与RA患者染色体核型异常检出率有显著性差异 (分别为 74 .4 %和 4 2 .5 % ,P <0 .0 0 1) ,IPSS预后好的染色体核型比例RA组 (6 5 .0 % )明显高于RCMD组 (2 4 .4 % )(P <0 .0 0 1) ,中等及差的染色体核型比例RCMD组 (分别为 4 8.9% ,2 6 .7% )明显高于RA组 (分别为 2 7.5 % ,7.5 % ) (P <0 .0 5 )。WHO分型与FAB分型一样 ,各亚型与IPSS危度分组有较好的相关性 ,WHO分型的RCMD低危组比例 (1.1% )较RA(10 .0 % )明显减低 (P <0 .0 5 ) ,RAEB Ⅱ高危组比例 (30 .5 % )较RAEB Ⅰ (0 )明显增高 (P <0 .0 0 1)。结论 pMDS的WHO分型较FAB分型与遗传学异常及预后的相关性更好

关 键 词:骨髓增生异常综合征  FAB分型  WHO分型  细胞遗传学  国际预后积分系统
修稿时间:2003-09-04

Karyotypic and IPSS grouping of primary myelodysplastic syndromes patients:a comparison between FAB-and WHO-classification
Ming-hua Yu,Shi-he Liu,Ying-qi Shao,Yu-shu Hao,Zhi-jian Xiao. Karyotypic and IPSS grouping of primary myelodysplastic syndromes patients:a comparison between FAB-and WHO-classification[J]. Chinese Journal of Hematology, 2004, 25(8): 482-485
Authors:Ming-hua Yu  Shi-he Liu  Ying-qi Shao  Yu-shu Hao  Zhi-jian Xiao
Affiliation:Institute of Hematology, CAMS & PUMC, Tianjin 300020, China.
Abstract:
OBJECTIVE: To compare the results of cytogenetic and IPSS grouping of primary myelodysplastic syndromes (pMDS) patients classified by FAB- or WHO classification. METHODS: Two hundred and thirty seven cases of pMDS who were previously classified according to FAB criteria were reclassified with WHO classification. A comparison was made between the results of the two classifications. RESULTS: For the detection rates of cytogenetic abnormality and its risks group, there was no difference among the FAB subgroups but the detection rate was different between the WHO refractory cytopenia with multilineage dysplasia (RCMD) and RA subgroups (74.4% and 42.5%, respectively) (P < 0.001). The percentage of good karyotype abnormalities in RA (65.0%) was higher than that in RCMD (24.4%) (P < 0.001), and the percentages of intermediate and poor karyotype abnormalities in RCMD (48.9% and 26.7%, respectively) were higher than that in RA (27.5% and 7.5%, respectively) (P < 0.05). There was a good correlation between the subgroups and IPSS risk groups for both the WHO classification and the FAB classification, but the WHO classification further reflected the differences between RCMD and RA and RAEB-I and RAEB-II subgroups. The percentage of low-risk group in RCMD (1.1%) was lower than that in RA (10.0%) (P < 0.05), and the percentage of high-risk group in RAEB-II (30.5%) was higher than that in RAEB-I(0) (P < 0.001). CONCLUSION: For the correlation between subgroups and cytogenetic abnormalities and IPSS risk groups, the WHO-classification is better than the FAB-classification.
Keywords:Myelodysplastic syndromes  FAB classification  WHO classification  Cyto-
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