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肿瘤诱导的骨软化症:漫长的诊断与康复之路

Tumour-induced osteomalacia: the long road to diagnosis and recovery.

作者信息

Vollmer Shobitha, Olsson Karin

机构信息

Department of Endocrinology, Skane University Hospital, Lund, Sweden

Department of Endocrinology, Skane University Hospital, Lund, Sweden.

出版信息

BMJ Case Rep. 2024 May 2;17(5):e258858. doi: 10.1136/bcr-2023-258858.

Abstract

Tumour-induced osteomalacia is caused by tumorous production of fibroblast growth factor 23 (FGF23) leading to urinary phosphate wasting, hypophosphataemia and decreased vitamin D activation. The resulting osteomalacia presents with muscle weakness and bone pain but progresses to multiple pathological fractures. Patients often remain undiagnosed for years with severe physical, psychological and economic ramifications. A young woman presented with multiple spontaneous fractures including bilateral femoral fractures. Laboratory tests revealed severe hypophosphataemia, elevated bone turnover markers and low to normal calcium and 25-hydroxy-vitamin D levels. Treatment with phosphate, alfalcalcidol, calcium and magnesium was initiated. Gallium-DOTATOC positron emission tomography imaging revealed a mass in the right foot and venous sampling of FGF23 from all extremities confirmed this tumour as the culprit. Biopsy and histology were consistent with a phosphaturic mesenchymal tumour, which was surgically resected. Phosphate levels quickly normalised postoperatively but a long convalescence with hungry bone syndrome, fracture healing and physical therapy followed.

摘要

肿瘤诱导的骨软化症是由肿瘤产生成纤维细胞生长因子23(FGF23)引起的,导致尿磷排泄增加、低磷血症和维生素D活化降低。由此产生的骨软化症表现为肌肉无力和骨痛,但会发展为多发性病理性骨折。患者常常多年未被诊断出来,会产生严重的身体、心理和经济后果。一名年轻女性出现多处自发性骨折,包括双侧股骨骨折。实验室检查显示严重低磷血症、骨转换标志物升高,钙和25-羟基维生素D水平低至正常。开始使用磷酸盐、阿法骨化醇、钙和镁进行治疗。镓-奥曲肽正电子发射断层扫描成像显示右脚有一个肿块,对所有肢体进行FGF23静脉采样证实该肿瘤为病因。活检和组织学检查结果与磷酸尿性间叶肿瘤一致,遂进行手术切除。术后磷酸盐水平迅速恢复正常,但随后出现了漫长的康复期,伴有饥饿性骨综合征、骨折愈合和物理治疗。

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