Abstract
Acute promyelocytic leukemia (APL) is a distinct subtype of acute myeloid leukemia (AML), which is characterized by the reciprocal t (15;17) (q24; q21) translocation, resulting in PML-RARA gene fusion. Therapy-related AML (t-AML) is a serious complication after cytotoxic and/or radiation therapy in many malignant diseases. In this report, MLL/KMT2A-MON2, with balanced chromosomal translocation t (11;12) (q23; q14), was identified as a novel fusion in a child transformed to t-AML after successful treatment of APL. This study emphasized that clinical monitoring with an integrated laboratory approach is essential for the diagnosis and treatment of t-AML.
Keywords:
MLL/KMT2A; MON2; acute promyelocytic leukemia; therapy-related acute myeloid leukemia.
© 2021 Wiley Periodicals LLC.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents / adverse effects*
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Antineoplastic Agents / therapeutic use
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Child, Preschool
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Chromosomes, Human, Pair 11 / genetics
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Chromosomes, Human, Pair 12 / genetics
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Histone-Lysine N-Methyltransferase / genetics*
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Humans
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Leukemia, Myeloid, Acute / chemically induced
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Leukemia, Myeloid, Acute / genetics*
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Leukemia, Promyelocytic, Acute / drug therapy*
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Leukemia, Promyelocytic, Acute / genetics
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Male
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Myeloid-Lymphoid Leukemia Protein / genetics*
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Oncogene Proteins, Fusion / genetics
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Proton-Translocating ATPases / genetics*
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Translocation, Genetic
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Whole Genome Sequencing
Substances
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Antineoplastic Agents
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KMT2A protein, human
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MON2 protein, human
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Oncogene Proteins, Fusion
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Myeloid-Lymphoid Leukemia Protein
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Histone-Lysine N-Methyltransferase
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Proton-Translocating ATPases