Abstract
A child with a known diagnosis of an autosomal dominant macrothrombocytopenia, Fechtner Syndrome, developed acute myeloid leukemia (AML). Recently the disease gene for the inherited macrothrombocytopenias has been identified as MYH9, encoding for non-muscle myosin heavy chain-A. MYH9 has never been associated with the development of acute leukemia, but MYH11 is disrupted in the M4 eosinophilia sub-type of AML (inv16). The patients leukemic blasts did carry the common t(8;21) which yields an AML1-ETO fusion protein that inhibits AML-1. Despite his thrombocytopenia, the patient successfully completed intensive bone marrow cytoreduction without significant bleeding complications and is now in remission for over 3 years.
(c) 2006 Wiley-Liss, Inc.
MeSH terms
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Antineoplastic Combined Chemotherapy Protocols / administration & dosage
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Blood Coagulation Disorders, Inherited / diagnosis
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Blood Coagulation Disorders, Inherited / drug therapy
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Blood Coagulation Disorders, Inherited / genetics*
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Blood Coagulation Disorders, Inherited / pathology
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Child, Preschool
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Chromosome Disorders / diagnosis
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Chromosome Disorders / drug therapy
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Chromosome Disorders / genetics*
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Chromosome Disorders / pathology
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Chromosomes, Human, Pair 21 / genetics
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Chromosomes, Human, Pair 8 / genetics
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Core Binding Factor Alpha 2 Subunit / genetics
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Humans
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Leukemia, Myeloid, Acute / diagnosis
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Leukemia, Myeloid, Acute / drug therapy
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Leukemia, Myeloid, Acute / genetics*
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Leukemia, Myeloid, Acute / pathology
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Male
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Molecular Motor Proteins / genetics
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Myosin Heavy Chains / genetics
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Oncogene Proteins, Fusion / genetics
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RUNX1 Translocation Partner 1 Protein
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Remission Induction
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Thrombocytopenia / diagnosis
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Thrombocytopenia / drug therapy
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Thrombocytopenia / genetics*
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Thrombocytopenia / pathology
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Translocation, Genetic
Substances
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AML1-ETO fusion protein, human
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Core Binding Factor Alpha 2 Subunit
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MYH9 protein, human
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Molecular Motor Proteins
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Oncogene Proteins, Fusion
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RUNX1 Translocation Partner 1 Protein
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Myosin Heavy Chains