The behavior of endometrial hyperplasia. A long-term study of “untreated” hyperplasia in 170 patients
- 15 July 1985
- Vol. 56 (2) , 403-412
- https://doi.org/10.1002/1097-0142(19850715)56:2<403::aid-cncr2820560233>3.0.co;2-x
Abstract
Endometrial curettings from 170 patients with all grades of endometrial hyperplasia, who did not undergo a hysterectomy for at least 1 yr, were evaluated in order to correlate the histopathologic features with behavior. Follow-up ranged from 1-26.7 yr (mean 13.4 yr). Cytologic and architectural alterations were analyzed separately in order to assess their respective roles in predicting the likelihood of progression to carcinoma. Classification of proliferative lesions based solely on the presence of cytologic atypia revealed that atypia was a discriminant factor. Proliferations lacking cytologic atypia were designated hyperplasia and those displaying atypia were designated atypical hyperplasia. Only 2 (1.6%) of 122 patients with hyperplasia progressed to carcinoma compared with 11 (23%) of women with atypical hyperplasia (P = 0.001). Subclassification of the 2 forms of hyperplasia (those with cytologic atypia and those without) was performed using the degree of architectural abnormalities. Hyperplasia and atypical hyperplasia displaying marked glandular complexity and crowding producing a back-to-back appearance were designated complex hyperplasia (CH) and complex atypical hyperplasia (CAH), respectively. Hyperplasia and atypical hyperplasia with lesser degrees of glandular complexity and crowding were designated simple hyperplasia (SH) and simple atypical hyperplasia (SAH), respectively. Progression to carcinoma occurred in 1 (1%) of 93 patients with SH, in 1 (3%) of 29 patients with CH, in 1 (8%) of the patients with SAH and in 10 (29%) of the patients with CAH. The differences between the 4 subgroups suggest a trend but are not statistically significant. The findings in this study provide a rationale for classifying noninvasive endometrial proliferations primarily on the basis of cytologic atypia, since this is the most useful criterion in predicting the likelihood of progression to carcinoma. In addition, the presence of concomitant architectural alterations appears to identify a particularly high-risk subgroup.This publication has 12 references indexed in Scilit:
- Stromal invasion in endometrial adenocarcinomaAmerican Journal of Obstetrics and Gynecology, 1984
- Evaluation of criteria for distinguishing atypical endometrial hyperplasia from well-differentiated carcinomaCancer, 1982
- Endometrial Lesions in Uteri Resected for Atypical Endometrial HyperplasiaAmerican Journal of Clinical Pathology, 1978
- Endometrial hyperplasia and carcinoma in-situGynecologic Oncology, 1974
- The teaching hospital experienceAmerican Journal of Obstetrics and Gynecology, 1963
- Precancerous lesions of the endometriumAmerican Journal of Obstetrics and Gynecology, 1963
- PRE‐MENOPAUSAL CYSTIC HYPERPLASIA AND ENDOMETRIAL CARCINOMBJOG: An International Journal of Obstetrics and Gynaecology, 1959
- Genesis of endometrial carcinoma.III. Carcinoma in situCancer, 1949
- Genesis of endometrial carcinoma.I. Study of Prior BiopsiesCancer, 1949
- Precursors of Corpus Carcinoma Estrogens and Adenomatous HyperplasiaAmerican Journal of Obstetrics and Gynecology, 1947