Cancer genetics and cytogenetics · 2006
Translocation (3;8)(q26;q24): a recurrent chromosomal abnormality in myelodysplastic syndrome and acute myeloid leukemia.
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Lin Pei, Medeiros L Jeffrey, Yin C Cameron, Abruzzo Lynne V
Аннотация
We identified a reciprocal translocation between chromosomes 3 and 8, with breakpoints at bands 3q26 and 8q24, in five patients with myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML). The t(3;8)(q26;q24) was the sole cytogenetic aberration in two patients, was associated with trisomy 13 in one patient, and occurred with monosomy 7 in two patients. In three patients, the AML or MDS developed 36, 52, and 57 months following chemotherapy for soft tissue sarcoma, mantle cell lymphoma, and diffuse large B-cell lymphoma, respectively; in these three patients, the neoplasms were considered to be therapy-related. All five patients displayed marked trilineage dysplasia and variable degrees of cytopenias, with marked thrombocytosis noted in one patient and a normal platelet count in another patient. All patients were treated with combination chemotherapy; at writing, four were still alive and one had died during a follow-up period ranging from 1 to 16 months. We conclude that the t(3;8)(q26;q24) is a recurrent translocation associated with therapy-related MDS/AML or de novo AML, and is frequently associated with monosomy 7.
Предметные рубрики MeSH
Acute DiseaseAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsChromosome AberrationsChromosomes, Human, Pair 3Chromosomes, Human, Pair 8FemaleHumansKaryotypingLeukemia, MyeloidLymphoma, B-CellLymphoma, Large B-Cell, DiffuseLymphoma, Mantle-CellMaleMiddle AgedMyelodysplastic SyndromesNeoplasm Recurrence, LocalSarcomaTranslocation, Genetic