Abstract

We report the case of a 66-year-old woman with tumor-induced osteomalacia (TIO) caused by fibroblast growth factor 23 (FGF-23) secreting mesenchymal tumor localized in a lumbar vertebra and review other cases localized to the axial skeleton. She presented with nontraumatic low back pain and spontaneous bilateral femur fractures. Laboratory testing was remarkable for low serum phosphorus, phosphaturia, and significantly elevated serum FGF-23 level. Magnetic resonance imaging (MRI) of the lumbar spine showed a focal lesion in the L-4 vertebra which was hypermetabolic on positron emission tomography (PET) scan. A computed tomography (CT) guided needle biopsy showed a low grade spindle cell neoplasm with positive FGF-23 mRNA expression by reverse transcriptase polymerase chain reaction (RT-PCR), confirming the diagnosis of a phosphaturic mesenchymal tumor mixed connective tissue variant (PMTMCT). The patient elected to have surgery involving anterior resection of L-4 vertebra with subsequent normalization of serum phosphorus. Including the present case, we identified 12 cases of neoplasms localized to spine causing TIO. To our knowledge, this paper represents the first documented case of lumbar vertebra PMT causing TIO. TIO is a rare metabolic bone disorder that carries a favorable prognosis. When a lesion is identifiable, surgical intervention is typically curative.

Highlights

  • Osteomalacia is a metabolic bone disorder characterized by impaired mineralization of osteoid matrix in mature bone

  • We report the case of a 66-year-old woman with tumor-induced osteomalacia (TIO) caused by a FGF-23 secreting mesenchymal tumor localized in the axial skeleton, in the fourth lumbar vertebra

  • Confirmation of phosphaturic mesenchymal tumor mixed connective tissue variant (PMTMCT) was obtained by computed tomography (CT) guided needle biopsy which revealed a low grade spindle cell neoplasm with positive FGF-23 mRNA expression by reverse transcriptase polymerase chain reaction (RT-PCR)

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Summary

Introduction

Osteomalacia is a metabolic bone disorder characterized by impaired mineralization of osteoid matrix in mature bone. Acquired forms of osteomalacia include renal tubulopathy (Fanconi’s type) and FGF-23 secreting PMTs; the latter referred to as TIO or oncogenic osteomalacia (OO). TIO is a rare paraneoplastic form of renal phosphate wasting that results in phosphaturia, a defect in vitamin D metabolism, and osteomalacia [1,2,3]. We report the case of a 66-year-old woman with TIO caused by a FGF-23 secreting mesenchymal tumor localized in the axial skeleton, in the fourth lumbar vertebra. We have identified only 12 cases of neoplasms localized to spine causing TIO. This paper represents the first documented case of lumbar vertebra PMT causing TIO

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