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Prostate-specific antigen and hormone receptor expression in male and female breast carcinoma
BACKGROUND: Prostate carcinoma is among the most common solid tumors to secondarily involve the male breast. Prostate specific antigen (PSA) and prostate-specific acid phosphatase (PSAP) are expressed in benign and malignant prostatic tissue, and immunohistochemical staining for these markers is oft...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954973/ https://www.ncbi.nlm.nih.gov/pubmed/20863373 http://dx.doi.org/10.1186/1746-1596-5-63 |
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author | Kraus, Teresa S Cohen, Cynthia Siddiqui, Momin T |
author_facet | Kraus, Teresa S Cohen, Cynthia Siddiqui, Momin T |
author_sort | Kraus, Teresa S |
collection | PubMed |
description | BACKGROUND: Prostate carcinoma is among the most common solid tumors to secondarily involve the male breast. Prostate specific antigen (PSA) and prostate-specific acid phosphatase (PSAP) are expressed in benign and malignant prostatic tissue, and immunohistochemical staining for these markers is often used to confirm the prostatic origin of metastatic carcinoma. PSA expression has been reported in male and female breast carcinoma and in gynecomastia, raising concerns about the utility of PSA for differentiating prostate carcinoma metastasis to the male breast from primary breast carcinoma. This study examined the frequency of PSA, PSAP, and hormone receptor expression in male breast carcinoma (MBC), female breast carcinoma (FBC), and gynecomastia. METHODS: Immunohistochemical staining for PSA, PSAP, AR, ER, and PR was performed on tissue microarrays representing six cases of gynecomastia, thirty MBC, and fifty-six FBC. RESULTS: PSA was positive in two of fifty-six FBC (3.7%), focally positive in one of thirty MBC (3.3%), and negative in the five examined cases of gynecomastia. PSAP expression was absent in MBC, FBC, and gynecomastia. Hormone receptor expression was similar in males and females (AR 74.1% in MBC vs. 67.9% in FBC, p = 0.62; ER 85.2% vs. 68.5%, p = 0.18; and PR 51.9% vs. 48.2%, p = 0.82). CONCLUSIONS: PSA and PSAP are useful markers to distinguish primary breast carcinoma from prostate carcinoma metastatic to the male breast. Although PSA expression appeared to correlate with hormone receptor expression, the incidence of PSA expression in our population was too low to draw significant conclusions about an association between PSA expression and hormone receptor status in breast lesions. |
format | Text |
id | pubmed-2954973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29549732010-10-15 Prostate-specific antigen and hormone receptor expression in male and female breast carcinoma Kraus, Teresa S Cohen, Cynthia Siddiqui, Momin T Diagn Pathol Research BACKGROUND: Prostate carcinoma is among the most common solid tumors to secondarily involve the male breast. Prostate specific antigen (PSA) and prostate-specific acid phosphatase (PSAP) are expressed in benign and malignant prostatic tissue, and immunohistochemical staining for these markers is often used to confirm the prostatic origin of metastatic carcinoma. PSA expression has been reported in male and female breast carcinoma and in gynecomastia, raising concerns about the utility of PSA for differentiating prostate carcinoma metastasis to the male breast from primary breast carcinoma. This study examined the frequency of PSA, PSAP, and hormone receptor expression in male breast carcinoma (MBC), female breast carcinoma (FBC), and gynecomastia. METHODS: Immunohistochemical staining for PSA, PSAP, AR, ER, and PR was performed on tissue microarrays representing six cases of gynecomastia, thirty MBC, and fifty-six FBC. RESULTS: PSA was positive in two of fifty-six FBC (3.7%), focally positive in one of thirty MBC (3.3%), and negative in the five examined cases of gynecomastia. PSAP expression was absent in MBC, FBC, and gynecomastia. Hormone receptor expression was similar in males and females (AR 74.1% in MBC vs. 67.9% in FBC, p = 0.62; ER 85.2% vs. 68.5%, p = 0.18; and PR 51.9% vs. 48.2%, p = 0.82). CONCLUSIONS: PSA and PSAP are useful markers to distinguish primary breast carcinoma from prostate carcinoma metastatic to the male breast. Although PSA expression appeared to correlate with hormone receptor expression, the incidence of PSA expression in our population was too low to draw significant conclusions about an association between PSA expression and hormone receptor status in breast lesions. BioMed Central 2010-09-23 /pmc/articles/PMC2954973/ /pubmed/20863373 http://dx.doi.org/10.1186/1746-1596-5-63 Text en Copyright ©2010 Kraus et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Kraus, Teresa S Cohen, Cynthia Siddiqui, Momin T Prostate-specific antigen and hormone receptor expression in male and female breast carcinoma |
title | Prostate-specific antigen and hormone receptor expression in male and female breast carcinoma |
title_full | Prostate-specific antigen and hormone receptor expression in male and female breast carcinoma |
title_fullStr | Prostate-specific antigen and hormone receptor expression in male and female breast carcinoma |
title_full_unstemmed | Prostate-specific antigen and hormone receptor expression in male and female breast carcinoma |
title_short | Prostate-specific antigen and hormone receptor expression in male and female breast carcinoma |
title_sort | prostate-specific antigen and hormone receptor expression in male and female breast carcinoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954973/ https://www.ncbi.nlm.nih.gov/pubmed/20863373 http://dx.doi.org/10.1186/1746-1596-5-63 |
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