肿瘤性骨软化致股骨颈不全骨折1例。

IF 0.4 Q4 ORTHOPEDICS Case Reports in Orthopedics Pub Date : 2021-10-06 eCollection Date: 2021-01-01 DOI:10.1155/2021/6668006
Yu Inoue, Tomoaki Fukui, Keisuke Oe, Shinya Hayashi, Teruya Kawamoto, Ryosuke Kuroda, Takahiro Niikura
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摘要

肿瘤诱导的骨软化症(TIO)是一种罕见的骨骼疾病,由间充质源性肿瘤纤维母细胞生长因子23 (FGF-23)分泌过多引起;TIO患者表现为骨折不全、进行性骨痛和骨折愈合延迟。在此,我们报告一例48岁男性左股骨颈不全骨折合并TIO。位于患者上颌窦的肿瘤已被切除;然而,由于肿瘤的位置,完全切除是不可能的。因此,患者的骨软化症持续存在,他在没有严重创伤的情况下经历了左股骨颈骨折。由于预计该患者骨折愈合延迟,我们使用带侧钢板的内固定物进行角度稳定,并使用多枚螺钉进行旋转稳定。虽然骨折愈合花了15个月的时间,但患者的术后过程平淡无奇,在术后30个月的最近一次随访中,他可以在没有任何症状或辅助的情况下行走。在TIO中,FGF-23的高分泌导致肾磷排泄增加,钙磷骨吸收增加,成骨细胞骨矿化减少,钙磷胃肠道吸收减少,导致骨折功能不全和骨折愈合延迟。由于其罕见和症状模糊,TIO的诊断经常被延迟。肿瘤完全切除是最佳治疗方法;然而,在不可能完全切除肿瘤的情况下,药物治疗可能不够,潜在的TIO病理,包括骨脆性,可能会持续存在。早期诊断对预防不完全性骨折有重要意义;然而,当骨折不可避免时,骨软化患者股骨颈骨折的手术治疗应考虑到骨折完全愈合的较长时间框架,因此使用具有足够稳定性的植入物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Case of Femoral Neck Insufficiency Fracture due to Tumor-Induced Osteomalacia.

Tumor-induced osteomalacia (TIO) is a rare skeletal disease caused by hypersecretion of fibroblast growth factor 23 (FGF-23) from neoplasms of mesenchymal origin; patients with TIO present with insufficiency fractures, progressive bone pain, and delayed fracture unions. Herein, we report the case of a 48-year-old man with an insufficiency fracture in his left femoral neck associated with TIO. The causative tumor located in the patient's maxillary sinus had been resected; however, complete resection was impossible due to the location of the tumor. Therefore, the patient's osteomalacia persisted, and he experienced a left femoral neck fracture in the absence of severe trauma. Because delayed fracture union was anticipated in this patient, we performed an internal fixation using an implant with a lateral plate for angular stability and multiple screws for rotational stability. Although fracture union took 15 months, the patient's postoperative course was uneventful, and he could walk without any symptoms or assistance at his most recent follow-up 30 months after surgery. In TIO, hypersecretion of FGF-23 leads to increased renal excretion of phosphorus, increased bone resorption of calcium and phosphorus, decreased osteoblastic bone mineralization, and decreased gastrointestinal absorption of calcium and phosphorus, leading to insufficiency fractures and delayed fracture unions. Diagnosis of TIO is often delayed due to its rarity and vague symptoms. Total resection of the causative tumor is the optimal treatment; however, in cases wherein complete tumor resection is impossible, drug therapy may be insufficient, and the underlying TIO pathology, including bone fragility, may persist. Early diagnosis of TIO is important for preventing insufficiency fractures; however, when fractures are unavoidable, the surgical treatment of femoral neck fractures in patients with osteomalacia should account for a longer time frame for complete fracture union and therefore utilize implants with sufficient stability.

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