Molecular characterization of der(15)t(11;15) as a secondary cytogenetic abnormality in acute promyelocytic leukemia with cryptic PML-RARα fusion on 17q

A case of acute promyelocytic leukemia (APL) with cryptic PML-RAR alpha fusion on 17q and add(15p) as a secondary abnormality rr as characterized using molecular cytogenetic techniques. Spectral karyotyping (SKY) short ed that chromosome 11 material was added to 15p, forming a der(15) t(11;15), which was refined to der(15)t(11;15)(q13.2:p13) with information obtained by comparative genomic hybridization (CGH). Interstitial insertion of chromosome 15 material into chromosome 17q was found by fluorescence in situ hybridization (FISH) with whole chromosome painting (WCP) probes. This study illustrates the necessity of a combination of molecular cytogenetics to decipher complex karyotypic abnormalities and cryptic translocations in leukemia. (C) 2000 Elsevier Science Inc. All rights reserved.