Metaplastic breast tumors with a dominant fibromatosis-like phenotype have a high risk of local recurrence
Open Access
- 15 May 1999
- Vol. 85 (10), 2170-2182
- https://doi.org/10.1002/(sici)1097-0142(19990515)85:10<2170::aid-cncr11>3.0.co;2-x
Abstract
BACKGROUND In the current study the authors describe the clinicopathologic characteristics of a low grade variant of spindle cell metaplastic tumors of the breast. Previously these tumors have been considered within a larger group recognized as metaplastic carcinoma, including cases with higher grade features. METHODS Breast tumors comprised predominantly of low grade spindle cells, with sparse low grade epithelial elements, were selected. Clinical features as well as macroscopic, microscopic, and immunohistochemical findings were reviewed with emphasis on the biologic behavior and the differential diagnosis from other spindle cell lesions. RESULTS Of 30 tumors fulfilling strict criteria, 20 contained squamous or glandular elements associated with the spindle cells. Ten tumors were comprised entirely of low grade spindle cells with limited clustered epithelioid cells. At the periphery, all tumors showed a proliferation of bland spindle cells infiltrating the adjacent parenchyma and mimicking fibromatosis. The epithelioid cells and some spindle cells expressed both vimentin and one or more cytokeratins. Seven of eight patients treated by excisional biopsy developed local recurrence, whereas only one of ten patients treated with wide excisional biopsy developed a local recurrence. No distant or regional metastases occurred. CONCLUSIONS The presence of limited clusters of epithelioid cells along with a dominant fibromatosis‐like pattern may be unique in the breast. The biologic potential of the fibromatosis‐like, spindle cell, metaplastic breast tumors most likely is defined by their major histologic phenotype; they are capable of local recurrence with no demonstrated distant spread or regional metastases, as in pure fibromatosis of the breast. Cancer 1999;85:2170–82. © 1999 American Cancer Society.Keywords
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