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Clinicopathological analysis of 38 male patients diagnosed with breast cancer.
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- Additional Information
- Source:
Publisher: IOS Press Country of Publication: Netherlands NLM ID: 8801277 Publication Model: Print Cited Medium: Internet ISSN: 1558-1551 (Electronic) Linking ISSN: 08886008 NLM ISO Abbreviation: Breast Dis Subsets: MEDLINE
- Publication Information:
Publication: Amsterdam : IOS Press
Original Publication: [New York, NY] : Elsevier, [c1987-
- Subject Terms:
- Abstract:
Background: Male breast cancer (MBC) accounts for one percent of all breast cancers. Due to the lack of awareness and routine screening programs, most patients present with systemic disease at the time of diagnosis with low overall survival.
Objectives: This study aims to investigate the prognostic factors of male breast cancer and its correlation with established prognostic parameters and patient outcomes.
Methods: Thirty-eight male breast cancer patients are identified from the MKA Breast Cancer Clinic database, and their corresponding clinical and pathological characteristics are obtained. Cut-off values of 1% and 10% are applied to further classify ER and PR results.
Results: Older men are more likely to develop MBC than younger men and are more likely to have spread to axillary lymph nodes. Invasive ductal carcinoma is a more common histologic type in MBC. All the tested patients have ER and PR positivity. Distant metastasis developed in 17/38 (44.7%) patients. Bone metastasis is seen commonly in metastatic MBC.
Conclusions: According to our cohort, MBC is seen in older males, presents in later stages, and shows hormone receptor positivity and a tendency to bone involvement. MBC is a heterogenous but distinct biological entity requiring a specific clinical and pathological approach.
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- Contributed Indexing:
Keywords: Male; breast cancer; prognostic parameters; survival
- Accession Number:
0 (Receptors, Progesterone)
- Publication Date:
Date Created: 20240216 Date Completed: 20240219 Latest Revision: 20240227
- Publication Date:
20240227
- Accession Number:
PMC10894578
- Accession Number:
10.3233/BD-230050
- Accession Number:
38363600
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