“…Despite their histologically benign appearance and negligible metastatic potential, desmoid tumors may exhibit an infiltrative and invasive behavior, becoming clinically significant, the result of pressure effects on vital structures. 2,3 Current treatment strategies rely on resection, 3 irradiation, 4,5 or medications to slow growth or induce tumor regression with nonsteroidal antiinflammatory drugs (sulindac, 6,7 indomethacin 7 ), interferon alfa-2b, 8,9 selective estrogen receptor modulators (SERMs; tamoxifen, toremifene), 1,6,7,10 and chemotherapy (doxorubicin, dacarbazine, and carboplatin; 11,12 methotrexate and vinblastine 13 ). These approaches have yielded inconsistent outcomes; additionally, surgery may stimulate regrowth of desmoid tumors.…”