Cancer genetics and cytogenetics · 2003
A unique clone involving multiple structural chromosome rearrangements in a myelodysplastic syndrome case.
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Yan Ju, Whittom Renaud, Delage Robert, Drouin Régen
Аннотация
In a young female patient presenting with a myelodysplastic syndrome (MDS), a unique clone involving six structural chromosome rearrangements was identified using G-banding and molecular cytogenetic techniques. Fifty GTG-banded metaphases from bone marrow were initially analyzed and all metaphases contained all of the six structural chromosome rearrangements. To further define the GTG-banded karyotype, a series of fluorescence in situ hybridization and primed in situ labeling experiments were performed and the karyotype was then characterized as: 46,XX,r(5)(p13q13),der(20)t(5;20),dup(11)(p11.2p15), r(11)(p15q25),del(13)(q14),idic(22)(p11). The patient quickly progressed to acute nonlymphocytic leukemia three months after the diagnosis and died of a hemorrhage in the brain parenchyma two months later. In this case, the multiple structural chromosome rearrangements conferred an obvious cellular proliferative advantage and indicated a very poor prognosis. Considering that multiple chromosome abnormalities associated with MDS transformation are often polyclonal, this unique clone involving six structural chromosome rearrangements make our case highly unusual.
Предметные рубрики MeSH
AdultAnemia, RefractoryBlast CrisisBone MarrowChromosome AberrationsChromosomes, Human, Pair 11Chromosomes, Human, Pair 13Chromosomes, Human, Pair 20Chromosomes, Human, Pair 22Chromosomes, Human, Pair 5Clone CellsDisease ProgressionFatal OutcomeFemaleHumansIn Situ Hybridization, FluorescenceKaryotypingLeukemia, Myeloid, AcutePrognosisRing ChromosomesTranslocation, Genetic