Desmoid fibromatosis of the breast: A case report and literature review

Pham Thuan Manh, Tran Ngoc Minh, Phan Thi Huyen

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Abstract

Desmoid Fibromatosis (DF) is a soft tissue tumor that aggressive locally but does not metastasize, often occurring in the mesentery, abdominal wall and extremities. DF of the breast is very rare, accounting for only 0.2% of breast tumors. The disease has symptoms very similar to breast cancer in clinical and imaging diagnosis, and has a high recurrence rate. This is a case of a female patient, 50 years old, with a left breast mass. Ultrasound and mammography of the mammary gland suspected as a malignant tumor, classified as BIRADS 5. Preoperative biopsy results as a cytologically bland spindle cell tumor, positive for Beta-Catenin, SMA, Ki67 (1%); negative for pan-CK, ER and p63 markers. The preoperative diagnosis was Desmoid Fibromatosis. Diagnosis after surgery confirmed it was Desmoid Fibromatosis, with positive resection margin. In summary, DF of the breast is a borderline mesenchymal, rare, recurrent tumor that is easily confused with cancer clinically, requires diagnosis based on histopathology, and requires extensive surgery.

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References

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