A rare case of atypical ossifying fibromyxoid tumor: multiple recurrences and metastasis
- PMID: 40221618
- DOI: 10.1007/s00256-025-04929-y
A rare case of atypical ossifying fibromyxoid tumor: multiple recurrences and metastasis
Abstract
Ossifying fibromyxoid tumor is a rare soft tissue mesenchymal neoplasm of unclear lineage and intermediate malignant potential, primarily arising in subcutaneous tissues of the limbs, head and neck, or trunk. Ossifying fibromyxoid tumors can be classified as typical, atypical, or malignant. While, most ossifying fibromyxoid tumors exhibit benign behavior, a subset demonstrates malignant tendencies, with a potential for local recurrence and distant metastasis. We report a case of an atypical ossifying fibromyxoid tumor in the soft tissue of the right elbow, characterized by multiple local recurrences and pulmonary metastases. This report details the clinical presentation, radiological findings, histopathological features, and therapeutic interventions, highlighting the challenges in managing this aggressive variant.
Keywords: Metastases; Ossifying fibromyxoid tumor; Radiological feature; Recurrence.
© 2025. The Author(s), under exclusive licence to International Skeletal Society (ISS).
Conflict of interest statement
Declarations. Ethics approval: All procedures performed in studies involving human participants were conducted in accordance with the ethical standards of the institutional and/or national research committee and in accordance with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent: Informed consent was obtained from the subject described in this report. Competing interests: The authors declare no competing interest.
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