[Hypophosphatemia and tumor-induced osteomalacia].
Catherine van der Rest, Etienne Cavalier, Laurent Colson, JF Kaux, J-M Krzesinski, Reginster Jy, Roland Hustinx, Pierre Delanaye
Abstract
Catherine van der Rest, Etienne Cavalier, Laurent Colson, JF Kaux, J-M Krzesinski, Reginster Jy, Roland Hustinx, Pierre Delanaye
Abstract
In this article, we will discuss about hypophosphatemia due to tumor-induced osteomalacia. This disease is characterized by severe muscular and articular tenderness inducing profound walking limitation. Clinical chemistry results show severe hypophosphatemia due to hyperphosphaturia. Fibroblast growth factor 23 (FGF-23) is abnormally high. Physiological role of FGF-23 is examined. We also consider the pathophysiology of tumor induced osteomalacia, the use of different investigations to localize the tumor and therapies available to treat this rare disease.
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In this article, we will discuss about hypophosphatemia due to tumor-induced osteomalacia. This disease is characterized by severe muscular and articular tenderness inducing profound walking limitation. Clinical chemistry results show severe hypophosphatemia due to hyperphosphaturia. Fibroblast growth factor 23 (FGF-23) is abnormally high. Physiological role of FGF-23 is examined. We also consider the pathophysiology of tumor induced osteomalacia, the use of different investigations to localize the tumor and therapies available to treat this rare disease.
Key concepts: Hypophosphatemia, Osteomalacia, Fibroblast growth factor 23, Medicine, Pathophysiology, Disease, Internal medicine, Pathology