Role of flow cytometry in diagnostics of myelodysplastic syndromes-beyond the WHO 2008 classification

被引:10
|
作者
Porwit, Anna [1 ,2 ]
机构
[1] Univ Hlth Network, Dept Lab Hematol, Toronto, ON M5G 2C4, Canada
[2] Karolinska Univ Hosp, Dept Pathol, Stockholm, Sweden
关键词
Flow cytometry; Myelodysplastic syndromes; Immunophenotyping; HUMAN-BONE-MARROW; ACUTE MYELOID-LEUKEMIA; MINIMAL RESIDUAL DISEASE; WORLD-HEALTH-ORGANIZATION; ACUTE ERYTHROID LEUKEMIA; CD34(+) CELLS; SCORING SYSTEM; PROGENITOR CELLS; FOLLOW-UP; T-CELLS;
D O I
10.1053/j.semdp.2011.06.003
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Multiparameter flow cytometry (FCM) is an excellent method to follow the expression patterns of differentiation antigens using monoclonal antibodies to surface and cytoplasmic proteins. Although several authors described various aberrant immunophenotypic features in the bone marrow of patients with myelodysplastic syndromes (MDS), the World Health Organization 2008 classification recommended that, only if 3 or more phenotypic abnormalities are found involving 1 or more of the myeloid lineages can the aberrant FCM findings be considered suggestive of MDS. In the absence of conclusive morphologic and/or cytogenetic features. FCM abnormalities alone were considered not sufficient to establish MDS diagnosis and further follow-up of the patients was recommended. Review of the literature gives accumulating evidence that FCM has become an important part of the integrated diagnostic work-up of patients with suspected MDS. Several studies have also reported FCM findings significant for prognosis and therapy choice in MDS patients. Technical progress in multicolor FCM and new analysis programs, together with ongoing efforts to standardize the methodology, will make it possible to apply FCM in individual risk assessment and choice of best therapy for MDS patients. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:273 / 282
页数:10
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