| Literature DB >> 16969146 |
Nobuyuki Koriyama1, Kengo Nishimoto, Takuro Kodama, Mitsuhiro Nakazaki, Yuichi Kurono, Hiroki Yoshida, Chuwa Tei.
Abstract
We herein describe the rare case of a 41-year-old woman with oncogenic osteomalacia due to a tumor in the maxillary sinus who presented with chronic general pain that had been gradually deteriorating. The patient's laboratory findings revealed hypophosphatemia due to renal phosphate wasting, an inappropriately low serum 1 alpha,25-dihydroxyvitamin D3 level for hypophosphatemia and an unusually high serum level of fibroblast growth factor 23 (FGF23). The causative tumor was surgically removed, resulting in a rapid resolution of the patient's biochemical abnormalities. An improvement of the abnormal multiple deposits on (99)Technetium-methylene diphosphonate bone scintigraphy and an increase in the bone metabolism markers suggested the development of bone remodeling within 49 days after the operation. The pathologic diagnosis of the tumor was a "phosphaturic mesenchymal tumor, mixed with a connective tissue variant." The expression of FGF23 was demonstrated in the tumor by the immunohistochemical techniques and a Western analysis.Entities:
Mesh:
Year: 2006 PMID: 16969146 DOI: 10.1097/00000441-200609000-00010
Source DB: PubMed Journal: Am J Med Sci ISSN: 0002-9629 Impact factor: 2.378