Author/Authors :
Falzetti، نويسنده , , Daniela and Vermeesch، نويسنده , , Joris R and Matteucci، نويسنده , , Caterina and Ciolli، نويسنده , , Stefania and Martelli، نويسنده , , Massimo F and Marynen، نويسنده , , Peter and Mecucci، نويسنده , , Cristina، نويسنده ,
Abstract :
Complex chromosomal rearrangements in malignant hemopathies frequently remain unclarified because of paucity of material for further fluorescence in situ hybridization analyses and/or lack of suitable probes. Chromosome microdissection (MD) can be an adequate approach to elucidate chromosome aberrations unrecognizable by conventional karyotyping. We applied MD in two patients with acute myeloid leukemia (AML) and unidentified chromosome changes at karyotype. Microdissection of a ring chromosome in an AML-M5 case revealed 21q polysomy. In an AML-M4 case, MD of an add(15p) disclosed a t(8;15) with over-representation of both 8q22 and 8q24 bands. YAC probes were helpful in showing duplication of the ETO gene at 8q22, and amplification of C-MYC, at 8q24.
