# Invasive Lobular Carcinoma of the Male Breast With BRCA2 Mutation

**Authors:** Misaki Abe, Fumi Saito, Naoko Honma, Yuko Tamaki, Mayu Goto, Katsunori Fukutake, Satoshi Sonobe, Yukiko Katagiri, Tomoko Shibayama, Hideaki Ogata

PMC · DOI: 10.1155/crip/3580444 · Case Reports in Pathology · 2026-02-26

## TL;DR

A rare case of male breast cancer with both ductal and lobular types, and a BRCA2 mutation, is reported and discussed.

## Contribution

The novelty lies in documenting a rare case of bilateral invasive lobular and ductal male breast cancer with a BRCA2 mutation.

## Key findings

- A male patient with bilateral breast cancer was found to have invasive ductal carcinoma on one side and invasive lobular carcinoma on the other.
- The patient was diagnosed with a BRCA2 gene mutation (c.331_347delinsC [p.Asn111Leufs∗5]).
- This case highlights the rare occurrence of lobular carcinoma in male breast cancer.

## Abstract

Male breast cancer (MBC) is a rare condition, accounting for < 1% of all breast cancer cases. Reports of bilateral synchronous MBC are even more uncommon. Although lobular carcinoma is generally absent in the male mammary gland, a few cases of lobular carcinoma in MBC have been documented, comprising 1%–2% of all MBC cases. A man in his 80s presented to our hospital with a mass on his left nipple. After detailed examination, he was diagnosed with invasive ductal carcinoma of the left breast and invasive lobular carcinoma of the right breast. Because he had a family history of breast cancer, he underwent genetic testing and was found to have a BRCA2 gene mutation (c.331_347delinsC [p.Asn111Leufs∗5]). Simultaneous surgery was performed for bilateral breast cancer. Although drug therapy and radiation therapy were recommended after the operation, the patient was under observation due to his advanced age. A brief literature review is presented in this section.

## Linked entities

- **Genes:** BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675]
- **Diseases:** breast cancer (MONDO:0004989), invasive ductal carcinoma (MONDO:0004953), invasive lobular carcinoma (MONDO:0005051)

## Full-text entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675] {aka BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** MBC (MESH:D018567), ulcer (MESH:D014456), jaw osteonecrosis (MESH:D059266), ILC (MESH:D018275), metastases (MESH:D009362), Breast (MESH:D061325), Contralateral breast cancer (MESH:D001943), IDC (MESH:D044584), liver dysfunction (MESH:D017093), uterine cancer (MESH:D014594), cancer metastasis (MESH:D009369), Klinefelter syndrome (MESH:D007713), Prostate cancer (MESH:D011471), pancreatic cancer (MESH:D010190), hereditary tumors (MESH:D013132), obesity (MESH:D009765), bleeding (MESH:D006470), GCT (MESH:D005870)
- **Chemicals:** denosumab (MESH:D000069448), H (MESH:D006859), N (MESH:D009584), C (MESH:D002244), E (MESH:D004540)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** c.331_347delinsC, [p.Asn111Leufs*5], [p.Asn111Leufs*5], c.331_347delinsC

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12936979/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12936979/full.md

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Source: https://tomesphere.com/paper/PMC12936979