HIDDEN MONOSOMY-7 IN ACUTE MYELOID-LEUKEMIA AND MYELODYSPLASTIC SYNDROME DETECTED BY INTERPHASE FLUORESCENCE IN-SITU HYBRIDIZATION
Citation
T. Arif et al., HIDDEN MONOSOMY-7 IN ACUTE MYELOID-LEUKEMIA AND MYELODYSPLASTIC SYNDROME DETECTED BY INTERPHASE FLUORESCENCE IN-SITU HYBRIDIZATION, Leukemia research, 20(9), 1996, pp. 709-716
Categorie Soggetti
Oncology,Hematology
SICI code
0145-2126(1996)20:9<709:HMIAMA>2.0.ZU;2-E
Abstract
Fifty patients [25 acute myeloid leukemia (AML) and 25 myelodysplastic
syndrome (MDS)], without monosomy 7 according to conventional cytogen
etics, were re-examined by fluorescence in situ hybridization (FISH).
Eleven (44.0%) patients with AML and nine (36.0%) with MDS showed hidd
en monosomy 7. Two samples who had both monosomy 7 and iso chromosome
17 were analyzed by dual color FISH to identify their clonal origin, a
nd showed that these two abnormalities can occur together or independe
ntly. Only one of 16 MDS patients without monosomy 7 transformed into
AML whereas four of eight MDS patients with the hidden monosomy 7 tran
sformed into AML, suggesting patients with this abnormality are more l
ikely to undergo transformation to AML. Copyright (C) 1996 Elsevier Sc
ience Ltd.