Peripheral blood neutrophil morphology reflects bone marrow dysplasia in myelodysplastic syndromes |
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Authors: | S. Widell,E. Hellstr m-Lindberg,Y. Kock,M. Lindberg, .
st,R. Hast |
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Affiliation: | S. Widell,E. Hellström-Lindberg,Y. Kock,M. Lindberg,Å. Öst,R. Hast |
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Abstract: | ![]() Dysplastic features of cells in peripheral blood and bone marrow were studied in 51 patients with myelodysplastic syndromes (MDS) to evaluate the significance of the degree of neutrophil granulation (G-score) and the percentage of pelgeroid polymorphs (ppp) in the peripheral blood, as indices of dysplastic changes in the bone marrow. There was a good correlation between peripheral blood and bone marrow findings, both for G-score figures (r = 0.92, P < 0.01) and ppp (r = 0.82, P < 0.01). Significantly lower G-score figures were found among patients with an increased percentage of bone marrow blasts (P < 0.05), while high ppp correlated with the presence of ring sideroblasts, the degree of bone marrow fibrosis, and findings of complex chromosomal abnormalities. Patients with a high degree of bone marrow dysplasia had significantly lower G-score (P < 0.01) and significantly higher ppp (P < 0.05) figures, than those with less pronounced myelodysplasia. In addition, extreme hypogranulation (G-score <150) or very high ppp (≥20%) was generally a sign of bi- and tri-lineage dysplasia in the bone marrow. The results thus show that quantitative estimation of peripheral blood polymorph dysplasia by G-score figures and ppp seems to reflect the total degree of bone marrow dysplasia in MDS and may serve as a complement to bone marrow evaluation when the diagnosis of MDS is difficult. © 1995 Wiley-Liss, Inc. |
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Keywords: | myelodysplastic syndromes granulocytes pseudo-Pelger hypogranulation bone marrow |
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