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254 Current Topics in Menopause, 2013, 254-314<br />

CHAPTER 10<br />

New Insights into Pathology of Endometrial Carcinoma at<br />

Menopause<br />

Efthimios Sivridis * and Alexandra Giatromanolaki<br />

Department of Pathology, Democritus University of Thrace Medical School, and<br />

University General Hospital of Alexandroupolis, Greece<br />

Abstract: The risk for endometrial carcinoma is directly related to age, with most cases<br />

occurring after the menopause. At this age group, the synthesis of estrogens continues,<br />

despite the decline of ovarian function. Androgen metabolism, in particular, is<br />

accelerated postmenopausally in all women, with the conversion of androstenedione to<br />

estrone. The reaction increases with increasing body weight. Thus, estrone, while a<br />

weak estrogen, by acting continuously and over a long period of time in its target tissue,<br />

the endometrium, may elicit the same biological response as does a potent estrogen such<br />

as estradiol in premenopausal women. This is evidenced by the fact that the<br />

postmenopausal endometrium, whilst atrophic, not only is potentially capable of giving<br />

genesis to endometrial carcinoma, but it does show a dramatic increase in the incidence<br />

of endometrial cancer during these years. Hence, endometrial carcinomas should no<br />

longer be regarded as “estrogen dependent” (Typed I carcinomas occurring in<br />

premenopausal women) or “estrogen independent” (Typed II carcinomas developing at<br />

menopause), but rather as neoplasms of high and low hormone dependency. Despite a<br />

general belief to the contrary, 55% of endometrial neoplasms occurring during<br />

menopause are G1 endometrioid adenocarcinomas, and almost 20% are G2-G3. A G1<br />

endometrioid adenocarcinoma developing in a postmenopausal woman, however, has<br />

the same favorable prognosis as does an adenocarcinoma of similar type and grade<br />

originating in young pre-menopausal women. On the other hand, Grade 3 endometrioid<br />

adenocarcinomas together with serous papillary and clear cell carcinomas (which by<br />

definition are also Grade 3) are of poor prognosis. Hence, is neither the state of the nonneoplastic<br />

endometrium (atrophic or hyperplastic) nor the menopausal status that<br />

determines the behaviour of an endometrial tumor, but rather is the histological type<br />

(whether endometrioid or non endometrioid) and the degree of tumor differentiation<br />

(whether low or high grade) that matters. On this basis, it is believed that the malignant<br />

potential of endometrial carcinomas can be defined precisely.<br />

Keywords: Adenocarcinoma, endometrium, menopause, pathogenesis, aetiology,<br />

androgens, histological type, endometrioid, non endometrioid, histological grade,<br />

prognosis, autophagy.<br />

*Address correspondence to Efthimios Sivridis: Department of Pathology, Democritus University of<br />

Thrace Medical School, and University General Hospital of Alexandroupolis, Alexandroupolis 68100,<br />

Greece; Tel: 0030-25510 75119; Fax: 0030-25510 30440; Email: esivrid@med.duth.gr.<br />

Volodymyr Dvornyk (Ed)<br />

All rights reserved-© 2013 <strong>Bentham</strong> <strong>Science</strong> Publishers

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