ProExC is a novel marker for distinguishing between primary endometrial and endocervical adenocarcinomas.
Autor: | Esheba GE; Department of Pathology, Faculty of Medicine, Tanta University, 3111 El Geesh Street, Tanta, Egypt. ghadaesheba@yahoo.com |
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Jazyk: | angličtina |
Zdroj: | Journal of the Egyptian National Cancer Institute [J Egypt Natl Canc Inst] 2013 Jun; Vol. 25 (2), pp. 87-93. Date of Electronic Publication: 2013 Feb 14. |
DOI: | 10.1016/j.jnci.2013.01.005 |
Abstrakt: | Background: Distinguishing endocervical adenocarcinoma (ECA) from endometrial adenocarcinoma (EMA) is clinically significant and cannot always be made on the basis of morphology alone or clinical findings. The aim of this study was to study the potential utility of ProExC as a new marker for cervical adenocarcinoma, and to evaluate a panel of monoclonal antibodies composed of p16, ER, PR, and vimentin, and assess their diagnostic value in distinguishing between ECA and EMA. Methods: Immunohistochemistry using monoclonal antibodies to ProExC, p16, estrogen receptor (ER), progesterone receptor (PR), and vimentin, was performed to examine 30 cases, including 10 ECAs and 20 EMAs. Results: Eight out of 10 cases (80%) of ECA were positive for ProExC, whereas only 2 cases of EMA (10%) were positive. The difference of ProExC expression in the two groups of malignancy was statistically significant (p=0.003). P16 was positive in 8 cases (80%) of ECAs and in 4 cases (20%) of EMAs. Estrogen receptor was negative in all cases of ECA, while it was positive in 95% of EMA. Progesterone receptor was positive in 2 cases (20%) of ECA and in 16 cases (80%) of EMA. Vimentin was positive in only one case (10%) of ECA, and in 16 cases (80%) of EMA. Conclusion: ProExC is a novel immunohistochemical marker for differentiating ECA from EMA and its inclusion in a panel of immunohistochemical markers including p16, ER, PR, and vimentin is recommended when there is morphological and clinical doubt as to the primary site of endocervical or endometrial origin. (Copyright © 2013. Production and hosting by Elsevier B.V.) |
Databáze: | MEDLINE |
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