Abstract
We report here the case of a woman with acute myeloid leukemia with some blast cells exhibiting acute promyelocytic leukemia (APL)-like hypergranular cytoplasm. The cytologic and cytochemical aspects as well as the mature myeloid phenotype and hemostasis disorders were consistent with the diagnosis of APL. However, no t(15;17), or RARalpha gene, MLL gene or PML gene rearrangement was observed, or any other cytogenetic clonal abnormality. Coexpression on blast cells of CD33 and CD56 without CD34, CD16 or HLA-DR, suggested a myeloid/natural killer cell acute leukemia.
MeSH terms
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Blast Crisis / pathology*
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Bone Marrow Cells / pathology*
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Cytoplasm / pathology
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Cytoplasmic Granules / pathology*
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DNA-Binding Proteins / genetics
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Diagnosis, Differential
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Female
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Histone-Lysine N-Methyltransferase
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Humans
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Leukemia, Promyelocytic, Acute / diagnosis*
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Leukemia, Promyelocytic, Acute / genetics
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Leukemia, Promyelocytic, Acute / pathology
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Middle Aged
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Myeloid-Lymphoid Leukemia Protein
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Neoplasm Proteins / genetics
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Nuclear Proteins*
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Peroxidase / analysis
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Promyelocytic Leukemia Protein
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Proto-Oncogenes*
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Receptors, Retinoic Acid / genetics
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Retinoic Acid Receptor alpha
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Transcription Factors / genetics
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Tumor Suppressor Proteins
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Zinc Fingers
Substances
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DNA-Binding Proteins
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KMT2A protein, human
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Neoplasm Proteins
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Nuclear Proteins
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Promyelocytic Leukemia Protein
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RARA protein, human
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Receptors, Retinoic Acid
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Retinoic Acid Receptor alpha
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Transcription Factors
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Tumor Suppressor Proteins
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PML protein, human
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Myeloid-Lymphoid Leukemia Protein
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Peroxidase
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Histone-Lysine N-Methyltransferase