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Ann Clin Lab Sci ; 41(2): 193-6, 2011.
Article in English | MEDLINE | ID: mdl-21844580

ABSTRACT

Gain-of-function mutations of the CKIT gene have been reported to specifically occur in core-binding factor (CBF) acute myeloid leukemia (AML) with a poor prognostic implication. Here we report a case of therapy-related AML with t(9;11)(p22;q23) who had CKIT mutation. A 48-year-old woman with breast cancer received partial mastectomy followed by 6 cycles of adjuvant chemotherapy and radiation therapy. At 28 months from the diagnosis of breast cancer, she was diagnosed as having AML with blasts 81% in bone marrow. Cytogenetic analysis revealed t(9;11)(p22;q23), and FISH showed 96.5% of MLL break-apart signals. RT-PCR study revealed MLL(11q23)/MLLT3(9p22) chimeric transcript. FLT3-ITD and NPM1 mutations were both negative. Unexpectedly, mutation analyses for CKIT identified D816Y mutation. The patient received induction chemotherapy and achieved complete remission at 1 month. To the best of our knowledge, this is the first report on CKIT mutation in therapy-related AML with MLL rearrangement.


Subject(s)
Leukemia, Myeloid, Acute/genetics , Mutation , Myeloid-Lymphoid Leukemia Protein/genetics , Nuclear Proteins/genetics , Proto-Oncogene Proteins c-kit/genetics , Breast Neoplasms/complications , Breast Neoplasms/therapy , Chromosomes, Human, Pair 11 , Chromosomes, Human, Pair 9 , Female , Histone-Lysine N-Methyltransferase , Humans , Leukemia, Myeloid, Acute/etiology , Leukemia, Myeloid, Acute/therapy , Middle Aged , Nucleophosmin , Translocation, Genetic
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