Abstract
Myelodysplastic syndromes (MDSs) comprise a heterogeneous group of homopoietic disorders sharing some probability of developing into overt leukemia [1]. According to glucose-6-phosphate dehydrogenase [9, 10], restriction fragment length polymorphism [6], and ras point mutation studies [7, 8], there is at least a subgroup of MDSs showing clonal growth of bone marrow cells. Up to now, however, it has been impossible to state that clonal cell growth is equivalent to malignant growth. It is conceivable that the progeny of an altered stem cell possesses some growth advantage over nonaltered cell populations but nevertheless remains subject to the regulation of steady state between growth and maturation. This regulation may be operating at an altered growth-to-maturation level. On the other hand, if preleukemia is a slowly progressing disorder, the very faint exponential character of the initial blast cell expansion may not become recognizable by standard laboratory examinations.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DAG, Gralnick HR, Sultan C (1982) Proposals for the classification of the myelodysplastic syndromes. Br J Haematol 51:189–199
Dörmer P, Hershko C, Voss R, Wilmanns W (1987) Myelodysplastic syndromes:evaluation of overt leukaemia by one or several steps of transformation. Br J Haematol 67:141–146
Dörmer P, Hershko C, Wilmanns W (1987) Mechanisms and prognostic value of cell kinetics in the myelodysplastic syndromes. Br J Haematol 67:147–152
Dörmer P, Schalhorn A, Wilmanns W, Hershko C (1987) Erythroid and myeloid maturation patterns related to progenitor assessment in the myelodysplastic syndromes. Br J Haematol 67:61–66
Fischer M, Mitrou PS, Hübner K (1976) Proliferative activity of undifferentiated cells (blast cells) in preleukaemia. Acta Haematol (Basel) 55:148–152
Janssen JWG, Buschle M, Layton M, Drexler HG, Lyons J, van den Berghe H, Heimpel H, Kubanek B, Kleihauer E, Mufti G, Bartram CR (1989) Clonal analysis of myelodysplastic syndromes:evidence of multipotent stem cell origin. Blood 73:248–254
Janssen JG, Steenvoorden ACM, Lyons J, Anger B, Bohlke JU, Bos JL, Seliger H, Bartram CR (1987) ras gene mutation in acute and chronic myelocytic leukemias, chronic myeloproliferative disorders, and myelodys-plastic syndromes. Proc Natl Acad Sci USA 84:9228–9232
Lyons J, Janssen JWG, Bartram C, Layton M, Mufti GJ (1988) Mutation of Ki-ras and N-ras oncogenes in myelodysplastic syndromes. Blood 71:1707–1712
Prchal JT, Throckmorton DW, Carroll III AJ, Fuson EW, Gams RA, Prchal JF (1978) A common progenitor for human myeloid and lymphoid cells. Nature 274:590–591
Raskind WH, Tirnmali N, Jacobson R, Singer J, Fialkow PJ (1984) Evidence for a multistep pathogenesis of a myelodysplastic syndrome. Blood 63:1318–1323
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1990 Springer-Verlag Berlin Heidelberg
About this paper
Cite this paper
Dörmer, P. (1990). Myelodysplastic Syndromes:Preleukemic or Early Leukemic Conditions?. In: Büchner, T., Schellong, G., Hiddemann, W., Ritter, J. (eds) Acute Leukemias II. Haematology and Blood Transfusion / Hämatologie und Bluttransfusion, vol 33. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-74643-7_1
Download citation
DOI: https://doi.org/10.1007/978-3-642-74643-7_1
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-50984-4
Online ISBN: 978-3-642-74643-7
eBook Packages: Springer Book Archive