Correia Joana, Machado Marino, Gonçalves Rui, Jonge Frederik, Micaelo Manuela, Pedrosa Carlos, Portela José
Department of Orthopedic Surgery and Traumatology, Hospital de Curry Cabral, Centro Hospitalar Universitário de Lisboa Central, Rua da Beneficência N. 8, 1069-166, Lisbon, Portugal.
Department of Nuclear Medicine, Hospital Lusíadas Lisboa, R.Abílio Mendes 12, 1500-458, Lisbon, Portugal.
Radiol Case Rep. 2021 Apr 9;16(6):1355-1362. doi: 10.1016/j.radcr.2021.03.015. eCollection 2021 Jun.
Phosphaturic mesenchymal tumors are the main cause of tumor-induced osteomalacia, a distinctive paraneoplastic syndrome mediated by overproduction of fibroblast growth factor 23, that leads to renal phosphate wasting and hypophosphatemia. Diagnosis of this mesenchymal tumors is difficult and usually delayed for several years. We present the case of a 70-years-old-male with generalized bone pain, multiple pathological fractures and persistent hypophosphatemia, diagnosed with tumor-induced osteomalacia after 4 years of the onset of symptoms. The tumor was localized in the forefoot using Gallium 68-DOTANOC positron emission tomography-computed tomography and successfully surgically treated. This case report highlights the importance of recognizing these rare tumors, as early diagnosis can prevent long-term morbidity.
磷酸尿性间叶肿瘤是肿瘤诱导性骨软化症的主要病因,这是一种由成纤维细胞生长因子23过度产生介导的独特副肿瘤综合征,可导致肾磷酸盐流失和低磷血症。这种间叶肿瘤的诊断困难,通常会延迟数年。我们报告一例70岁男性,有全身骨痛、多处病理性骨折和持续性低磷血症,症状出现4年后被诊断为肿瘤诱导性骨软化症。使用镓68 - DOTANOC正电子发射断层扫描 - 计算机断层扫描将肿瘤定位在前足,并成功进行了手术治疗。本病例报告强调了认识这些罕见肿瘤的重要性,因为早期诊断可预防长期发病。