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TUMOR-INDUCED INPOPHOSPHATEMIC OSTEOMALACIA : Report of Three Cases

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Abstract

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SUMMARY
Tumor-induced hypophosphatemic osteomalacia has been rarely reported. The clinical
and radiographic features of tumor-induced hypophosphatemic osteomalacia are similar to
that of hyperparathyroidism, but it is distinguished from hyperparathyroidism on the
basis of its different biochemical features, such as normal seam calcium concentration,
decreased serum phosphorus concentration, and elevated serum alkaline phosphatase
level.
The importance of laboratory features of the metabolic disease is emphasized. Since
resection of a coexisting tumor without additional treatment lead to prompt a increase.
In seam phosphorus, recovery of clinical symptom, and remineralization of bone, an
accurate diagnosis should be established as quickly as possible.
We have recently experienced three cases of tumor-induced hypophosphatemic
osteomalacia. The clinical, radiographic, and laboratory features were dramatically
improved after resection of the coexisting tumors.

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