From September 1, 1989, to November 30, 1991, 175 menopausal breast ca
ncer patients treated with tamoxifen were followed at the authors' ins
titutions. During this period, 16 (9.1%) underwent total abdominal hys
terectomy and bilateral salpingo-oophorectomy, for various indications
, Of these, 10 (62.5%) had either uni- or bilateral ovarian tumors, Th
e analysis of surgical findings showed an incidence of 5.7% (10/175) o
varian tumors among all the patients. In 2 (?OB), the ovarian masses d
isplayed enlargement over a relatively short period while on treatment
, In 5 (50%) patients, the findings were bilateral. All tumors were de
tectable by ultrasonography, except four serous cystadenomas found in
3 women, The mean duration of tamoxifen treatment was 36.6 +/- 24.9 (r
ange 9-86) months. The rate of 5.7% for ovarian tumors, in this select
ed group of patients, is four to five times higher than that reported
for similar pathologic conditions detected by general screenings viith
ultrasonographic scans among nonselected, asymptomatic, and untreated
postmenopausal rt omen. Two possibilities should be considered in the
development of ovarian tumors coinciding with tamoxifen treatment; (1
) women with breast malignancy are prone to develop benign or malignan
t ovarian tumors in relation to genetic factors, regardless of tamoxif
en treatment; and (2) tamoxifen may stimulate enlargement of such tumo
rs and may even cause them. (C) 1996 Academic Press, Inc.