Eline M P Cremers, Theresia M Westers, Canan Alhan, Claudia Cali, Mariëlle J Wondergem, Pino J Poddighe, Gert J Ossenkoppele, Arjan A van de Loosdrecht
European journal of cancer (Oxford, England : 1990) 2016 FebMandatory for the diagnosis of myelodysplastic syndromes (MDS) is the presence of dysplasia in >10% of cells within one or more cell lineages or presence of >15% ring sideroblasts or presence of MDS-associated cytogenetic (CG) abnormalities. Discrimination between neo-plastic and non-neoplastic causes of cytopenias can be challenging when dysplastic features by cytomorphology (CM) are minimal and CG abnormalities are absent or non-discriminating from other myeloid neoplastic disorders. This study evaluated a standard diagnostic approach in 379 patients with unexplained cytopenias and highlights the additional value of flow cytometry (FC) in patients with indeterminate CM and CG. CM reached no clear-cut diagnosis in 44% of the patients. Here, CG was able to identify two additional patients with MDS; other CG results did not reveal abnormalities or were not contributory. Based on the FC results, patients without a diagnosis by CM and CG were categorized 'no MDS-related features' (65%), 'limited number of MDS-related changes' (24%), and 'consistent with MDS' (11%). Patients were followed over time in an attempt to establish or confirm a diagnosis (median follow-up 391 d, range 20-1764). The specificity (true negative) of MDS-FC analysis calculated after follow-up was 95%. FC can aid as a valuable tool to exclude MDS when CM and additional CG are not conclusive in patients with cytopenia. Copyright © 2015 Elsevier Ltd. All rights reserved.
Eline M P Cremers, Theresia M Westers, Canan Alhan, Claudia Cali, Mariëlle J Wondergem, Pino J Poddighe, Gert J Ossenkoppele, Arjan A van de Loosdrecht. Multiparameter flow cytometry is instrumental to distinguish myelodysplastic syndromes from non-neoplastic cytopenias. European journal of cancer (Oxford, England : 1990). 2016 Feb;54:49-56
PMID: 26720403
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