Chromosome studies of lipomas have revealed an extensive cytogenetic h
eterogeneity. To investigate the frequencies of previously recognized
cytogenetic subgroups and to find out if more recurrent rearrangements
can be identified, we have analyzed cytogenetically short-term tissue
cultures of 237 samples from 188 adipose tissue tumors obtained from
142 patients. Only one of 58 tumors from 18 patients with multiple lip
omas (more than two tumors) had karyotypic changes. Among the sporadic
lipomas, 20 tumors had supernumerary ring chromosomes of unknown orig
in, 55 had different aberrations involving chromosome segment 12q13-15
, 11 had changes of 6p or chromosome 13, but no rings or 12q13-15 chan
ges, and-14 had various other aberrations. Ring chromosomes were found
in all cytogenetically abnormal lipomas histologically classified as
atypical and in nine tumors classified as typical lipoma or spindle ce
ll lipoma. Recombinations between 12q13-15 and a few other bands or se
gments were seen more than once: 3q27-28 (15 tumors), 2p22-24 and 2q35
(four tumors), 1p32-34 and 13q12-14 (three tumors), and 5q33 (two tum
ors). Recombinations of 12q13-15 with 2q35 and 13q12-14 have not been
described before. Of eight tumors with chromosome 13 aberrations, five
had loss of 13q material. Aberrations of 12q13-15, 6p, and/or chromos
ome 13 were found simultaneously in nine tumors. Two to four samples f
rom the same tumor were investigated in 29 tumors with clonal aberrati
ons. Thirteen of these tumors displayed clonal evolution; also noted i
n another 17 tumors in which only one sample had been investigated. Th
us clonal evolution occurred in 30% of the tumors and was particularly
frequent in atypical lipomas. (C) 1994 Wiley-Liss, Inc.