Abstract
Angiosarcoma is a rare soft tissue tumor of the breast. It occurs in both a primary form without a known precursor, and a secondary form that has been associated to a history of irradiated breast tissue. These forms differ in many ways including median age, precipitating factors, and presentation. Both forms have a malignant behavior and a poor prognosis. The endeavor of this paper is to review what is known about the presentation, diagnostic and therapeutic modalities to date.
Original language | English (US) |
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Pages (from-to) | 28-34 |
Number of pages | 7 |
Journal | Gland Surgery |
Volume | 3 |
Issue number | 1 |
DOIs | |
State | Published - Feb 2014 |
Externally published | Yes |