A Case Report of Synchronous Multicentric Breast Carcinoma With Biologically Discordant Phenotypes: Luminal A and Triple-Negative Subtypes

We present the case of a 45-year-old Caucasian woman diagnosed with synchronous bicentric breast cancer of differing molecular phenotypes in the same breast. The first tumor, an invasive ductal carcinoma (G1), was estrogen and progesterone receptor-positive and HER2-negative, with a low proliferative index (Ki67 10%). A second lesion, located in a different quadrant and appearing within weeks after biopsy, exhibited a triple-negative phenotype and a higher proliferative index (Ki67 30%). Both tumors were classified as stage IA. Due to the multicentric nature of disease, the patient underwent mastectomy with sentinel node biopsy and immediate reconstruction. Genetic testing was negative for BRCA1/2, CHEK2, and PALB2 mutations, though familial cancer history suggested a possible hereditary syndrome (FCC suspicion). This case underscores the complexity of managing multicentric breast cancer with discordant receptor status and raises questions about the role of biopsy sites in tumor development.

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Publication Details

Journal
Cureus
Published
2025-08-09
DOI
https://doi.org/10.7759/cureus.89666
Primary Topic
Breast Cancer Treatment Studies
Type
article
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article

A Case Report of Synchronous Multicentric Breast Carcinoma With Biologically Discordant Phenotypes: Luminal A and Triple-Negative Subtypes

Michał Gajewski, Barbara Sławińska, Oliwia Sysło, Zuzanna Błecha et al.
Cureus
Breast Cancer Treatment Studies
article

A Case Report of Synchronous Multicentric Breast Carcinoma With Biologically Discordant Phenotypes: Luminal A and Triple-Negative Subtypes

Michał Gajewski, Barbara Sławińska, Oliwia Sysło, Zuzanna Błecha, Konrad Haraziński, Weronika Goliat, Izabela Jastrzębska, Nikola Rubik, Maksym Gmur, Nicole Maryniak, Przemyslaw R Dalski-Szelag
article en

Abstract

We present the case of a 45-year-old Caucasian woman diagnosed with synchronous bicentric breast cancer of differing molecular phenotypes in the same breast. The first tumor, an invasive ductal carcinoma (G1), was estrogen and progesterone receptor-positive and HER2-negative, with a low proliferative index (Ki67 10%). A second lesion, located in a different quadrant and appearing within weeks after biopsy, exhibited a triple-negative phenotype and a higher proliferative index (Ki67 30%). Both tumors were classified as stage IA. Due to the multicentric nature of disease, the patient underwent mastectomy with sentinel node biopsy and immediate reconstruction. Genetic testing was negative for BRCA1/2, CHEK2, and PALB2 mutations, though familial cancer history suggested a possible hereditary syndrome (FCC suspicion). This case underscores the complexity of managing multicentric breast cancer with discordant receptor status and raises questions about the role of biopsy sites in tumor development.

CureusVol. 17(8)
Poznan University of Medical Sciences (PL), Medical University of Silesia (PL), Academy of Fine Arts in Katowice (PL), Międzyleski Szpital Specjalistyczny w Warszawie (PL), WSB University (PL), Children's Specialized Hospital (US)
Openalex Percentile: Top 74%
Breast Cancer Treatment Studies
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