Huang Zichun, Liu Guohong
Department of Radiology, Zhongnan Hospital of Wuhan University, Wuhan University, 169 East Lake Road, Wuchang District, Wuhan, 430071, Hubei Province, China.
Skeletal Radiol. 2025 Apr 13. doi: 10.1007/s00256-025-04929-y.
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.
骨化性纤维黏液样肿瘤是一种罕见的软组织间叶性肿瘤,其谱系不明,具有中等恶性潜能,主要发生于四肢、头颈部或躯干的皮下组织。骨化性纤维黏液样肿瘤可分为典型、非典型或恶性。虽然大多数骨化性纤维黏液样肿瘤表现为良性行为,但一部分显示出恶性倾向,有局部复发和远处转移的可能。我们报告一例发生于右肘部软组织的非典型骨化性纤维黏液样肿瘤,其特征为多次局部复发和肺转移。本报告详细阐述了临床表现、影像学表现、组织病理学特征及治疗干预措施,突出了处理这种侵袭性变异型肿瘤所面临的挑战。