| Literature DB >> 26935241 |
Nicolas Duployez1,2, Olivier Nibourel3,4, Benoît Ducourneau3, Nathalie Grardel3, Thomas Boyer3,4, Claire Bories5, Stéphane Darre6, Valérie Coiteux5, Céline Berthon4,5, Claude Preudhomme3,4, Catherine Roche-Lestienne4,7.
Abstract
We report a case of myeloproliferative neoplasm (MPN) with an atypical t(9;22;15)(p24;q11;q21) translocation, leading to a BCR-JAK2 fusion, associated with a trisomy of chromosome 8 in clonal evolution at karyotype. Patient's evolution was marked by an aggressive clinical course with rapid progression to blast phase within the first year after diagnosis. Examination of matched chronic phase and blast crisis samples by SNP-array karyotyping identified secondary acquired cryptic genetic events at the time of lymphoblastic transformation, including biallelic IKZF1 alteration and EBF1 and CDKN2A/B codeletions. This case is the first report describing acquisition of secondary genetic events leading to acute lymphoblastic progression in a rare MPN with BCR-JAK2 fusion.Entities:
Keywords: BCR-JAK2; IKZF1; SNP-array; acute leukemia; cytogenetics; myeloproliferative neoplasms
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Year: 2016 PMID: 26935241 DOI: 10.1111/ejh.12752
Source DB: PubMed Journal: Eur J Haematol ISSN: 0902-4441 Impact factor: 2.997