Clonal karyotypic alterations of chromosome 6 in three uterine smooth
muscle tumors are reported. In all cases an apparently identical break
point on the short arm of chromosome 6 was found. Two cases displayed
the histologic features of cell-rich myomas with severe nuclear atypia
but no clear evidence for malignancy. The remaining case was a primar
y uterine leiomyosarcoma of an 80-year-old patient showing an apparent
ly balanced reciprocal chromosomal translocation, t(1;6)(p32-33;p21.3)
, as the sole karyotypic abnormality. This type of aberration has not
been reported before in leiomyosarcomas. Because of the nuclear atypia
in the other myomas with a breakpoint involving the short arm of chro
mosome 6 we feel that this cytogenetically recognizable but rare subgr
oup of uterine smooth muscle tumors warrants a careful clinical follow
-up.