Abstract
This report describes a unique case of acute myeloid leukemia with hypergranular cytoplasm and t(X;11)(q24;q23). The breakpoint on 11q23 was identified within the MLL gene. The hypergranular cytoplasm of leukemic cells and the associated coagulopathy resembled a characteristic of acute promyelocytic leukemia, despite the absence of RARalpha gene rearrangement in this case. The Xq24 site possibly played a role in this atypical blast phenotype.
MeSH terms
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Child
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DNA-Binding Proteins / genetics*
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Disseminated Intravascular Coagulation / complications
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Gene Rearrangement
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Histone-Lysine N-Methyltransferase
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Humans
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Karyotyping
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Leukemia, Myeloid / complications
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Leukemia, Myeloid / drug therapy
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Leukemia, Myeloid / genetics*
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Male
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Myeloid-Lymphoid Leukemia Protein
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Proto-Oncogenes*
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Remission Induction
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Transcription Factors*
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Translocation, Genetic*
Substances
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DNA-Binding Proteins
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KMT2A protein, human
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Transcription Factors
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Myeloid-Lymphoid Leukemia Protein
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Histone-Lysine N-Methyltransferase