Abstract
Myelodysplastic syndrome (MDS) is a progressive preleukaemic condition caused by an abnormality of haemopoietic stem cells [1,10] and characterized by both genetic and functional changes [3,4]. Dysmegakaryocyto-poiesis is a common feature in MDS and results in thrombocytopenia in about 50% of cases [4]. Megakaryocyte colony formation was found to be defective in many MDS patients [5,6]. Futhermore, MDS plasma displayed a low ability to support the clonal growth of normal megakaryocytopoietic progenitors [13]. Although the number of marrow megakaryocytes may be decreased, normal or increased, they are often morphologically abnormal with reduced size (micromegakaryocytes) [2,14,19] and small hypo- or nonlobulated nuclei [13,16]. The degree of dysmegakaryocytopoiesis along with the degree of dysgranulocytopoiesis has been introduced as an additional criterion aiming at better prediction of patients’ survival than that based on the French-American-British Group (FAB) classification alone [1,18].
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© 1993 Springer-Verlag Berlin Heidelberg
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Podolak-Dawidziak, M., Geddesa, D., Bowen, D. (1993). Megakaryocytopoiesis in Patients with Myelodysplastic Syndromes. In: Fleischer, J. (eds) Leukemias. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-77083-8_2
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DOI: https://doi.org/10.1007/978-3-642-77083-8_2
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