Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, India.
Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Neurol India. 2019 Sep-Oct;67(5):1334-1340. doi: 10.4103/0028-3886.271274.
Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome of certain mesenchymal tumors which secrete fibroblast growth factor-23 (FGF-23) responsible for causing features of hypophosphatemia and osteomalacia in these patients. Most of them involve the appendicular skeleton and occasionally the craniofacial regions. Involvement of spine is exceedingly rare. Through this paper, the authors present a rare case of a 71-year-old male with TIO due to a lesion in the cervical spine (right C2 lamina) which was proven to be a phosphaturic mesenchymal tumor-mixed connective tissue type on histopathology. This is the fifth reported case of TIO localized to the cervical spine. The patient underwent a hemilaminectomy and gross total resection of the tumor following which he made a gradual but steady recovery and does not have any recurrence 24 months after surgery. The authors not only provide a comprehensive literature review of all 18 spinal cases reported till date but also discuss the management of these patients in light of the published literature.
肿瘤相关性骨软化症(TIO)是某些间叶肿瘤的罕见副瘤综合征,这些肿瘤分泌成纤维细胞生长因子-23(FGF-23),导致患者出现低磷血症和骨软化症的特征。它们大多涉及四肢骨骼,偶尔涉及颅面区域。脊柱受累极为罕见。通过本文,作者报告了一例罕见的 71 岁男性 TIO 病例,其病因是颈椎(右侧 C2 椎板)病变,组织病理学证实为磷酸尿基质肿瘤-混合结缔组织型。这是第五例报道的颈椎 TIO 病例。患者接受了半椎板切除术和肿瘤大体全切除,此后逐渐但稳定地恢复,术后 24 个月无复发。作者不仅提供了迄今为止所有 18 例脊柱病例的全面文献复习,还根据已发表的文献讨论了这些患者的治疗方法。