Background. The majority of karyotypes observed in osteosarcomas (OS)
and chondrosarcomas (CS) are complex. Specific chromosomal abnormaliti
es have not yet been characterized in either tumor except for a ring c
hromosome in parosteal OS. The purpose of this study was to determine
recurrent chromosomal abnormalities and establish a possible correlati
on between the cytogenetic changes and the pathologic findings. Method
s. Ten OS and nine CS were cytogenetically analyzed. Tumor samples wer
e obtained from patients having a resection or incisional biopsy. Cyto
genetic study of short term cell cultures included harvesting and G-ba
nding, which were performed by routine methodologies. Results. Clonal
abnormalities were observed in six OS and six CS. Modal chromosome num
bers ranged from near diploid to near tetraploid in both types of tumo
rs. The structural rearrangements observed in OS involved mostly chrom
osomes 1, 2, 6, 12, and 17. Nonreciprocal translocations were the most
frequent event. Two OS had a single clonal abnormality involving 11p1
5 and 14q32, respectively. Double minute chromosomes were observed in
three cases. In CS, the most frequent structural abnormalities were no
nreciprocal translocations and deletions involving numerous chromosome
s. Rearrangements of Ip together with other abnormalities were observe
d in four CS. Conclusions. The karyotypes were usually complex consist
ing of numerical and structural changes, particularly in high grade tu
mors. Rearrangements of 11p15 and 14q32 in OS and possibly Ip in CS we
re found as primary cytogenetic aberrations. Cytogenetic analysis in m
ore cases of OS and CS together with molecular studies are necessary t
o characterize further the consistent genetic changes in these tumors.