Author/Authors :
Emberger، نويسنده , , W and Behmel، نويسنده , , A and Tschernigg، نويسنده , , M and Seewann، نويسنده , , H.L and Petek، نويسنده , , Peter M. Kroisel، نويسنده , , P.M and Wagner، نويسنده , , K، نويسنده ,
Abstract :
We report a 59-year-old, male, chronic myeloid leukemia patient with a rare variant Philadelphia (Ph) translocation t(9;10;22)(q34;q22;q11). Fluorescence in situ hybridization with whole chromosome paints was used to confirm the cytogenetic findings. With a BCR/ABL-specific probe, the known rearrangement on the derivative chromosome 22 was found. The prognostic implications as well as the relevance of the additional breakpoint region 10q22 are discussed.