# Case Report: Metaplastic breast carcinoma with osseous and chondrodifferentiation in liver metastasis: a rare case and review of literature

**Authors:** Wenfang Li, Qin Ou, Tian-xiang Zhang, Bin Bin Long, Ke Zhou, Lun Hua Zhao

PMC · DOI: 10.3389/fonc.2025.1437887 · Frontiers in Oncology · 2025-10-02

## TL;DR

A rare case of metaplastic breast carcinoma with unusual liver metastasis is reported, highlighting diagnostic challenges and treatment outcomes.

## Contribution

This case report adds to the limited literature on metaplastic breast carcinoma with osseous and chondrodifferentiation in liver metastasis.

## Key findings

- Core needle biopsy may not accurately diagnose metaplastic carcinoma with mesenchymal differentiation.
- Neoadjuvant chemotherapy with epirubicin, cyclophosphamide, or paclitaxel may be ineffective in some cases.
- Timely surgical excision of a single liver metastasis can lead to long-term progression-free survival.

## Abstract

Metaplastic carcinoma of the breast with mesenchymal differentiation (MCMD) is a type of metaplastic breast carcinoma (MpBC) that is very rare and aggressive. The present case provides valuable information for clinicians on this MpBC.

A 41-year-old woman visited our hospital for a palpable painless mass in the left breast. Core needle biopsy (CNB) was performed, and the pathological result was infiltrating ductal carcinoma. Epirubicin (100 mg/m2) + cyclophosphamide (600 mg/m2) for four cycles was given. Color Doppler ultrasound examination indicated no obvious change in the size of the left breast mass. We changed to paclitaxel (175 mg/m2) for two cycles. Re-examination on April 26, 2018 with color Doppler ultrasound indicated that the tumor diameter increased to 8.39 cm × 8.07 cm × 6.19 cm. Radical resection of the left breast carcinoma was performed on June 04, 2018. The postoperative pathological results showed that the left breast tumor was composed of carcinoma and sarcoma components, without nerves and vascular invasion. The immunohistochemistry results were as follows: ER: (−), PR: (−), HER2: (−), CK5/6 (+), CK7: (+), E-cadherin (+), Ki67: 40% (+), P120: (+), P53 diffuse +, P63: (+), and S100 partially positive, GATA-3: (+). Four cycles of vinorelbine (25 mg/m2) + cisplatin (40 mg/m2) were performed after the operation. Enhanced CT indicated a 6.0 cm × 4.6 cm mass in the liver on January 1, 2019 through regular review, and liver lobectomy confirmed that metastasis originated from sarcoma components, together with bone and cartilage differentiation. The immunohistochemistry results indicated the following: ER (−), PR (−), GATA-3 (−), CD34 (+), P63 (−), CK8 (−), P40: (−), and vimentin: (+). The patient received oral anlotinib 12 mg once a day, with 2 weeks on/1 week off for eight cycles. The patient survived and showed no signs of recurrence at the follow-up visit.

This case indicated that CNB may not always give an accurate diagnosis for MCMD. Neoadjuvant chemotherapy with epirubicin, cyclophosphamide, or paclitaxel for MCMD may not be effective for patients showing no sensitivity to these drugs. In addition, regular postoperative follow-up plays an important role in the early detection of remote metastasis, and timely surgical excision of a single metastatic lesion in the liver can lead to long-term progression-free survival (PFS).

## Linked entities

- **Proteins:** EREG (epiregulin), PGR (progesterone receptor), ERBB2 (erb-b2 receptor tyrosine kinase 2), ck56 (hypothetical protein), KRT7 (keratin 7), shg (shotgun), Mki67 (antigen identified by monoclonal antibody Ki 67), CTNND1 (catenin delta 1), TP53 (tumor protein p53), RPE65 (retinoid isomerohydrolase RPE65), S100A1 (S100 calcium binding protein A1), GATA3 (GATA binding protein 3), CD34 (CD34 molecule), KRT8 (keratin 8), IL9 (interleukin 9), PRELID1 (PRELI domain containing 1)
- **Chemicals:** Epirubicin (PubChem CID 41867), Cyclophosphamide (PubChem CID 2907), Paclitaxel (PubChem CID 36314), Vinorelbine (PubChem CID 5311497), Cisplatin (PubChem CID 5460033), Anlotinib (PubChem CID 25017411)
- **Diseases:** Metaplastic breast carcinoma (MONDO:0006043), Breast carcinoma (MONDO:0004989)

## Full-text entities

- **Genes:** CD34 (CD34 molecule) [NCBI Gene 947], CTNND1 (catenin delta 1) [NCBI Gene 1500] {aka BCDS2, CAS, CTNND, P120CAS, P120CTN, p120}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, TP63 (tumor protein p63) [NCBI Gene 8626] {aka AIS, B(p51A), B(p51B), EEC3, KET, LMS}, KRT8 (keratin 8) [NCBI Gene 3856] {aka CARD2, CK-8, CK8, CYK8, K2C8, K8}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}, S100A1 (S100 calcium binding protein A1) [NCBI Gene 6271] {aka S100, S100-alpha, S100A}, VIM (vimentin) [NCBI Gene 7431]
- **Diseases:** sarcoma (MESH:D012509), carcinoma (MESH:D009369), Metaplastic carcinoma of the breast (MESH:D001943), liver metastasis (MESH:D009362), infiltrating ductal carcinoma (MESH:D044584)
- **Chemicals:** cyclophosphamide (MESH:D003520), paclitaxel (MESH:D017239), Epirubicin (MESH:D015251), cisplatin (MESH:D002945), anlotinib (MESH:C000625192), vinorelbine (MESH:D000077235)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12527893/full.md

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Source: https://tomesphere.com/paper/PMC12527893