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Acute megakaryoblastic leukaemia with extreme thrombocytosis and p190bcr/ablrearrangement

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Abstract

Acute megakaryoblastic leukaemia (AML-M7) is an uncommon disease, composing 0.5–1.2% of newly diagnosed adult acute myeloid leukaemias (AML). It is characterised by higher incidence and complexity of cytogenetic abnormalities. We report a rare case of Philadelphia (Ph) chromosome-positive AML-M7, presenting with extreme thrombocytosis and having a poor outcome. The diagnosis was established on the basis of morphological and flow cytometry data for megakaryoblastic proliferation in the bone marrow. Cytogenetics revealed 47,XX,+8,t(9;22)(q34;q11), and p190BCR-ABL-rearrangement was detected. MDR1-gene overexpression was not demonstrated; however, the patient was resistant to therapy and died in 6 months. The reported case contributes to the overt heterogeneity of Ph-positive AMLs, which warrants further investigation and understanding.

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Acknowledgements

All authors contributed equally to this work. We thank Dr. Angel Stoimenov, Krassimira Boikova and Antonia Georgieva for their excellent assistance. The study was supported by a grant from the Ministry of Education and Science, Bulgaria.

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Correspondence to M. Guenova.

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Balatzenko, G., Guenova, M., Zechev, J. et al. Acute megakaryoblastic leukaemia with extreme thrombocytosis and p190bcr/ablrearrangement. Ann Hematol 83, 381–385 (2004). https://doi.org/10.1007/s00277-003-0783-1

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  • DOI: https://doi.org/10.1007/s00277-003-0783-1

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