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Phyllodes tumors (PTs) account for less than 1% of breast tumors, and malignant PTs account for even less. Here, we described an unusual case of malignant PT with mixed liposarcoma (myxoid liposarcoma [MLP] and pleomorphic liposarcoma [PLP]). A 52-year-old woman discovered a small lump in her left breast. Twenty years later, the lump suddenly grew within 1 month. Mammography showed space-occupying lesions of the left breast. Histologically, the tumor was characterized by hypercellular stroma covering the epithelium and protrusion of the myoepithelium into the cyst to form a lobulated structure; regions of loose mucus and hypercellular structures alternated. A region of peripheral benign fibroadenoma was also observed, and many stellate and spindle cells or signet ring-like cells were identified in loose areas. Some areas showed a characteristic thin branching vascular pattern. In the cell-rich area, adipocytes and odd megakaryocytes were observed. Atypical mitotic figures were observed in the cell-rich and mucus areas (16 mitoses/10 high-power fields [HPF] and 2 mitoses/10 HPF, respectively). In the immunohistochemical analysis, a small number of tumor cells were positive for AE1/3 and vimentin, whereas all cells were negative for cytokeratin 34βE12, E-cadherin, p63, estrogen receptor, progesterone receptor, human epidermal growth factor receptor 2, and S-100, ruling out the possibility of metaplastic carcinoma. Interestingly, cyclin-dependent kinase 4, mouse double minute 2 (MDM2), and p16 were strongly positive in both loose mucus and cell-rich areas. However, the fluorescence in situ hybridization test results showed that MDM2 was not amplified. Combined with morphological characteristics, these findings supported that the tumor was a mixed malignant PT with MLP and PLP. Our patient did not receive radiation therapy, and after 47 months of follow-up, no recurrence or metastasis occurred. This case report serves to expand the morphologic spectrum of mixed malignant PT with liposarcoma.
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http://dx.doi.org/10.2147/OTT.S298379 | DOI Listing |
Clin Cancer Res
September 2025
University of Michigan-Ann Arbor, Ann Arbor, MI, United States.
Purpose: Liposarcoma (LPS) is the most common soft tissue sarcoma. Well-differentiated LPS (WDLPS) can progress to dedifferentiated LPS (DDLPS), a more aggressive form with higher metastatic potential and poor response to existing therapies. Progress in understanding and treating LPS has been limited.
View Article and Find Full Text PDFCureus
August 2025
Department of Surgery, Ayub Medical College, Abbottabad, PAK.
This report presents the case of a 62-year-old male who presented with a two-month history of right flank pain and decreased appetite. Clinical evaluation revealed a palpable, non-tender mass in the right flank, while laboratory tests demonstrated mild anemia (hemoglobin 9.3 g/dL) with otherwise normal renal function.
View Article and Find Full Text PDFMedicine (Baltimore)
August 2025
Department of Pathology, Guangxi Medical University Cancer Hospital, Nanning, China.
Rationale: Dedifferentiated liposarcoma (DDLPS) is a subtype of sarcoma that originates from atypical lipomatous tumor/well-differentiated liposarcoma and undergoes varying degrees of dedifferentiation. DDLPS can occur either concurrently with or after atypical lipomatous tumor/well-differentiated liposarcoma, with the dedifferentiated component predominantly consisting of high-grade sarcomas. Notably, only approximately 10% of DDLPS cases present as purely low-grade sarcomas.
View Article and Find Full Text PDFLancet Reg Health Eur
October 2025
Departments of Medicine & Surgery, Gustave Roussy Cancer Campus, Villejuif, France.
Background: Liposarcomas (LPS) are among the most common sarcomas, but gather a diversity of rare to ultrarare molecular subtypes whose presentations and natural histories are partially characterized. The aim of the work was to describe the presentation and outcome of the different LPS histotypes from the NETSARC+ registry.
Methods: NETSARC+ (netsarc.
Zhonghua Bing Li Xue Za Zhi
July 2025
Ningbo Clinical Pathology Diagnosis Center, Ningbo 315100, China.
To investigate the clinicopathological characteristics, as well as diagnostic and differential diagnostic criteria of perinephric myxoid pseudotumor of fat (PMPF). Five cases of PMPF were retrospectively collected from the departmental files of Zhejiang Provincial People's Hospital (4 cases) and Ningbo Clinical Pathology Diagnosis Center (1 cases) from January 2020 to December 2023, the clinical, morphological, and immunohistochemical characteristics were analyzed. Fluorescence in-situ hybridization (FISH) was utilized to detect the amplification status of MDM2 and the rearrangement status of DDIT3.
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