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Oncogenic osteomalacia: loss of hypophosphatemia might be the key to avoid misdiagnosis.

Authors :
Chang CV
Conde SJ
Luvizotto RA
Nunes VS
Bonates MC
Felicio AC
Lindsey SC
Moraes FH
Tagliarini JV
Mazeto GM
Kopp P
Nogueira CR
Source :
Arquivos brasileiros de endocrinologia e metabologia [Arq Bras Endocrinol Metabol] 2012 Nov; Vol. 56 (8), pp. 570-3.
Publication Year :
2012

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.

Details

Language :
English
ISSN :
1677-9487
Volume :
56
Issue :
8
Database :
MEDLINE
Journal :
Arquivos brasileiros de endocrinologia e metabologia
Publication Type :
Academic Journal
Accession number :
23295300
Full Text :
https://doi.org/10.1590/s0004-27302012000800018