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A novel t(2;17) in transformation of essential thrombocythemia to acute myelocytic leukemia.

Lazarevic, Vladimir Lj (author)
Umeå universitet,Medicin
Tomin, Dragica (author)
Jankovic, Gradimir M (author)
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Antic, Darko (author)
Dencic, Marija (author)
Gotic, Mirjana (author)
Boskovic, Darinka (author)
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 (creator_code:org_t)
2004
2004
English.
In: Cancer Genetics and Cytogenetics. - 0165-4608 .- 1873-4456. ; 148:1, s. 77-9
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A transformation of essential thrombocythemia to acute myelocytic leukemia (AML), myelodysplastic syndrome, or agnogenic myelocytic metaplasia is a relatively rare event. It occurs in 1%-4.5% of all patients with either treated or untreated essential thrombocythemia. Cytogenetic changes in the transformation to AML are common. We report the case of a patient treated for essential thrombocythemia with hydroxyurea for 49 months. He developed AML with a t(2;17), which to our knowledge has not been described in the literature.

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