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

Author:

Chang Claudia V.1,Conde Sandro J.1,Luvizotto Renata A. M.1,Nunes Vânia S.1,Bonates Milla C.1,Felicio Andre C.2,Lindsey Susan C.1,Moraes Flávia H.1,Tagliarini José V.1,Mazeto Glaucia M. F. S.1,Kopp Peter3,Nogueira Célia R.1

Affiliation:

1. Universidade Estadual de São Paulo, Brazil

2. Universidade Federal de São Paulo, Brazil

3. Metabolism and Molecular Medicine Northwestern University, United States

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. Arq Bras Endocrinol Metab. 2012;56(8):570-3

Publisher

FapUNIFESP (SciELO)

Subject

General Medicine,Endocrinology, Diabetes and Metabolism

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