A Normal FGF23 Does Not Preclude Tumor-Induced Osteomalacia.
Neeharika NandamSadia EjazWilliam AhrensMaya StynerPublished in: JBMR plus (2020)
Tumor-induced osteomalacia (TIO) is a rare cause of impaired bone mineralization mediated by the osteocyte-derived, phosphaturic hormone: fibroblast growth factor 23 (FGF23). The case is presented of a previously healthy 45-year-old man who developed fragility fractures at multiple sites (initially metatarsals, eventually ribs, hips, spine, scapula, and sacrum) resulting in rapid functional deterioration, weakness, and the inability to bear weight and ambulate without a walker. Workup for secondary causes of bone loss was negative except for mild hypogonadotropic hypogonadism with normal pituitary MRI and hypophosphatemia that persisted despite aggressive supplementation. Testosterone was initiated but discontinued 6 months later because of deep vein thrombosis and pulmonary embolism, likely provoked by his new sedentary state, in addition to smoking history and possibly testosterone usage. Serum FGF23 was nonelevated at 138 mRU/mL (44-215). A genetic panel for OI variants was negative for a causal mutation. At the age of 48, 3 years after his initial fracture, he was referred to our academic endocrine clinic. We ruled out additional mutations that lead to hypophosphatemic rickets, including phosphate-regulating endopeptidase homolog, X-linked. PET/CT looking for a potential TIO locus revealed uptake in the left suprapatellar recess. Biopsy was consistent with a phosphaturic mesenchymal tumor. FGF23 was repeated for a preoperative baseline and now found to be elevated at 289 mRU/mL. In retrospect, it is likely that the initial level was inappropriately elevated for the degree of hypophosphatemia. After resection, he experienced marked improvement in physical function, decreased pain, and resolution of renal phosphate wasting. The principals of establishing a robust clinical diagnosis of TIO should be emphasized, excluding other entities and avoiding pitfalls in the interpretation of laboratory testing. © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research.
Keyphrases
- bone loss
- pulmonary embolism
- pet ct
- replacement therapy
- physical activity
- high glucose
- copy number
- quantum dots
- diabetic rats
- bone mineral density
- chronic pain
- inferior vena cava
- primary care
- stem cells
- bone marrow
- visible light
- single cell
- weight loss
- computed tomography
- randomized controlled trial
- neuropathic pain
- soft tissue
- spinal cord
- patients undergoing
- risk assessment
- positron emission tomography
- magnetic resonance
- ultrasound guided
- spinal cord injury
- gene expression
- body composition
- contrast enhanced
- climate change
- hip fracture