| Literature DB >> 23295300 |
Claudia V Chang1, Sandro J Conde, Renata A M Luvizotto, Vânia S Nunes, Milla C Bonates, Andre C Felicio, Susan C Lindsey, Flávia H Moraes, José V Tagliarini, Glaucia M F S Mazeto, Peter Kopp, Célia R Nogueira.
Abstract
Diagnosing oncogenic osteomalacia is still a challenge. The disorder is characterized by osteomalacia caused by renal phosphate wasting and low serum concentration of 1,25-dihydroxyvitamin D3 occurring in the presence of a tumor that produces high levels of fibroblast growth factor 23. However, it is possible that the disease is much more misdiagnosed than rare. We present the case of a 42-year-old man with a long-term history of undiagnosed progressive muscle weakness. His laboratory results mainly showed low serum phosphate. Surgical removal of a nasal hemangiopericytoma that had been diagnosed five years earlier, brought him to a symptom-free condition. Even though knowing the underlying etiology would explain his osteomalacia, the patient sought medical help from countless physicians for five consecutive years, and only after adequate treatment a rewarding outcome was achieved.Entities:
Mesh:
Year: 2012 PMID: 23295300 DOI: 10.1590/s0004-27302012000800018
Source DB: PubMed Journal: Arq Bras Endocrinol Metabol ISSN: 0004-2730