Endometrial cancer detection
Results: There were selected, for these immunohistochemistry reactions, 22 cases of simple hyperplasia without atypia, 26 cases of endometrial cancer detection hyperplasia without endometrial cancer detection, 23 cases of endometrial adenocarcinoma of endometrioid type, well differentiated, 22 cases of endometrial adenocarcinoma of endometrioid type, moderately differentiated, and 19 cases of non-endometrioid adenocarcinomas represented by nine clear cells and 10 serous endometrial adenocarcinomas.
Conclusions: Endometrial hyperplasia, especially complex endometrial cancer detection hyperplasia with atypia, increase the risk for endometrial adenocarcinoma, and their early detection becomes mandatory under cancer prevention. Well-differentiated endometrioid endometrial adenocarcinomas GI in the endometrial cancer detection group also showed a higher content of ER and PR compared to the endometrial moderately-differentiated endometrioid endometrial adenocarcinomas GII.
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In non-endometrioid adenocarcinomas, represented by clear-cell endometrial adenocarcinomas, the ER content was reduced and the PR expression was negative. Serous adenocarcinomas failed to show an immunohistochemically expression for ER and PR. Endometrial carcinoma with trophoblastic differentiation: an aggressive form of uterine cancer.
Endometrial cancer detection Navigare în articole
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