Leukemická transformácia polycytemia vera po liecbe s hydroxyureou s abnormalitami chromozómu c. 17
[Leukemic transformation of polycythemia vera after treatment with hydroxyurea and chromosome 17 abnormalities]
Language Slovak Country Czech Republic Media print
Document type Case Reports, English Abstract, Journal Article
PubMed
11045151
- MeSH
- Leukemia, Myeloid, Acute etiology genetics MeSH
- Chromosome Deletion * MeSH
- Hydroxyurea adverse effects therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Chromosomes, Human, Pair 17 genetics MeSH
- Polycythemia Vera complications drug therapy MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Female MeSH
- Publication type
- English Abstract MeSH
- Journal Article MeSH
- Case Reports MeSH
- Names of Substances
- Hydroxyurea MeSH
The authors present two patients with polycythemia vera where they recorded after several years' treatment with hydroxyurea development of acute myeloblastic leukaemia. In both instances they found, associated with leukaemia, abnormalities of chromosome no.17, in one case meeting criteria of the so-called 17p-syndrome. Progression of polycythemia vera into acute leukaemia is explained by the possible association with the long-term use of the drug and loss of chromosomal material (short arm of chromosome 17), the part where genes important in the process of leukaemogenesis are located. The authors draw attention to contemplated long-term administration of hydroxyurea to young patients with polycythemia vera. As cytogenetic analysis is a suitable method for evidence of progressing polycythemia vera into acute leukaemia, dynamic follow up of chromosomal changes is necessary, in particular in patients where long-term treatment with hydroxyurea is assumed.