| Literature DB >> 26136801 |
Sayantan Ray1, Partha Pratim Chakraborty1, Kaushik Biswas1, Sujoy Ghosh1, Satinath Mukhopadhyay1, Subhankar Chowdhury1.
Abstract
This paper shows a case of oncogenic osteomalacia in a 35-year-old man who presented with a 2-year history of generalized pain and progressive weakness of lower limbs, eventually became bed bound. At admission he had severe hip pain resulting from atraumatic femoral neck fractures. Laboratory investigations revealed hypophosphatemia, hyperphosphaturia, normocalcemia, elevated alkaline phosphatase, and normal serum levels of parathormone and 25-hydroxyvitamin D. Serum FGF-23 was elevated. Imaging showed osteoporosis and insufficiency fractures of the femoral neck. Whole body functional imaging failed to reveal any areas of increased activity. However, on computed tomography (CT) and magnetic resonance (MR) imaging, a tumor was discovered at left nasal cavity. The patient was treated with phosphate supplements and vitamin D, but his hypophosphatemia persisted. The tumor was surgically removed. Histologically, the tumor was diagnosed as variant of a sinonasal hemangiopericytoma-like tumor. After surgery, his symptoms were relieved and biochemical parameters normalized.Entities:
Keywords: fibroblast growth factor 23; hemangiopericytoma; hypophosphatemia; nasal tumor; oncogenic osteomalacia
Year: 2015 PMID: 26136801 PMCID: PMC4469232 DOI: 10.11138/ccmbm/2015.12.1.065
Source DB: PubMed Journal: Clin Cases Miner Bone Metab ISSN: 1724-8914