TY - JOUR
T1 - Prognostically favorable 'mitotically active' smooth-muscle tumors of the uterus. A clinicopathologic study of ten cases
AU - Perrone, T.
AU - Dehner, L. P.
PY - 1988/1/1
Y1 - 1988/1/1
N2 - We evaluated the clinicopathologic features of 22 smooth-muscle tumors of the uterine corpus that had at least five mitoses per 10 high-power fields (HPF) in the most active areas. Ten women were alive and well without tumor recurrence 15 months to 11 years after diagnosis (median, 6 years); these patients were referred to as the 'clinically benign' group. The other 12 women had 'clinically malignant' disease: 9 died of recurrent or metastatic tumor 3 months to 4.5 years after diagnosis (median, 16 months), and 3 are alive with disease 4-12 months after diagnosis. Significant clinical and pathologic differences were observed between patients in the 'benign' and 'malignant' groups. We found that mitotic activity in the range of 5 to 15 mitoses per 10 HPF was not a reliable predictor of aggressive behavior in tumors that lacked marked cytologic atypia and that by all other clinical and pathologic criteria were leiomyomas. An unfavorable prognosis among the mitotically active neoplasms could be predicted by a constellation of clinico-pathologic features, including postmenopausal status, a clinical or intraoperative impression of cancer by the surgeon, extension of tumor beyond the uterine corpus, size greater than 10 cm, marked cytologic atypia, invasive borders, necrosis, and mitotic counts exceeding 20 per 10 HPF.
AB - We evaluated the clinicopathologic features of 22 smooth-muscle tumors of the uterine corpus that had at least five mitoses per 10 high-power fields (HPF) in the most active areas. Ten women were alive and well without tumor recurrence 15 months to 11 years after diagnosis (median, 6 years); these patients were referred to as the 'clinically benign' group. The other 12 women had 'clinically malignant' disease: 9 died of recurrent or metastatic tumor 3 months to 4.5 years after diagnosis (median, 16 months), and 3 are alive with disease 4-12 months after diagnosis. Significant clinical and pathologic differences were observed between patients in the 'benign' and 'malignant' groups. We found that mitotic activity in the range of 5 to 15 mitoses per 10 HPF was not a reliable predictor of aggressive behavior in tumors that lacked marked cytologic atypia and that by all other clinical and pathologic criteria were leiomyomas. An unfavorable prognosis among the mitotically active neoplasms could be predicted by a constellation of clinico-pathologic features, including postmenopausal status, a clinical or intraoperative impression of cancer by the surgeon, extension of tumor beyond the uterine corpus, size greater than 10 cm, marked cytologic atypia, invasive borders, necrosis, and mitotic counts exceeding 20 per 10 HPF.
UR - http://www.scopus.com/inward/record.url?scp=0023865375&partnerID=8YFLogxK
U2 - 10.1097/00000478-198801000-00001
DO - 10.1097/00000478-198801000-00001
M3 - Article
C2 - 3337336
AN - SCOPUS:0023865375
SN - 0147-5185
VL - 12
SP - 1
EP - 8
JO - American Journal of Surgical Pathology
JF - American Journal of Surgical Pathology
IS - 1
ER -