We examined 10 malignant fibrous histiocytomas (MFHs) using metaphase
preparations. Six tumors showed clonal structural and/or numerical chr
omosomal aberrations, and four tumors had normal karyotypes. For the m
ost part, chromosomes 1, 3, 6, 9, 12, 16, 18, and 20 were involved in
structural aberrations. The breakpoint regions most frequently were in
1p32, 3p25, and the centromeric region of chromosomes 1 and 16. There
was a conspicuous loss in chromosome 18. We detected ring chromosomes
in two tumors. One tumor showed a high percentage of near-haploid cel
ls. Our results show many parallels to data which have already been pu
blished. MFHs include a broad spectrum of tumors of widely different h
istology and clinical course. So it is not surprising to find a cytoge
netic diversity of chromosomal aberrations in this study. (C) Elsevier
Science Inc., 1998.