{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,25]],"date-time":"2026-08-25T08:28:22Z","timestamp":1787646502525,"version":"build-2736575974"},"reference-count":24,"publisher":"SAGE Publications","issue":"4","license":[{"start":{"date-parts":[[2024,11,18]],"date-time":"2024-11-18T00:00:00Z","timestamp":1731888000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"funder":[{"name":"MSK NIH","award":["MSK NIH Funded Grant# P30 CA08748"],"award-info":[{"award-number":["MSK NIH Funded Grant# P30 CA08748"]}]}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Int J Surg Pathol"],"published-print":{"date-parts":[[2025,6]]},"abstract":"<jats:p>\n                    Ossifying fibromyxoid tumor (OFMT) is a rare soft tissue neoplasm of uncertain origin, exhibiting a wide clinical and morphological spectrum. It ranges from benign forms, which typically behave indolently, to malignant lesions with significant recurrence and metastatic potential. The majority of OFMTs harbor\n                    <jats:italic toggle=\"yes\">PHF1<\/jats:italic>\n                    gene rearrangements, with\n                    <jats:italic toggle=\"yes\">EP400<\/jats:italic>\n                    being the most common fusion partner. Herein, we present a patient with malignant metastatic OFMT, with the very rare\n                    <jats:italic toggle=\"yes\">PHF1::FOXR2<\/jats:italic>\n                    fusion, and discuss the potential clinical implications of this genetic alteration.\n                  <\/jats:p>","DOI":"10.1177\/10668969241295349","type":"journal-article","created":{"date-parts":[[2024,11,18]],"date-time":"2024-11-18T05:43:06Z","timestamp":1731908586000},"page":"1010-1015","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":1,"title":["Aggressive Malignant Ossifying Fibromyxoid Tumor With a Rare\n                    <i>PHF1::FOXR2<\/i>\n                    Fusion: A Case Report and Literature Review"],"prefix":"10.1177","volume":"33","author":[{"given":"Antonia","family":"Syrnioti","sequence":"first","affiliation":[{"name":"Aristotle University of 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