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Orthopaedics · Metabolic bone disease: oncogenic osteomalacia
Sample itemA 50-year-old man has progressive bone pain, proximal muscle weakness and pseudofractures. Serum phosphate is low with excessive urinary phosphate loss, calcitriol is low, and there is no family history. A small mesenchymal tumour is found in the soft tissue of the foot. Which mediator causes the syndrome?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Fibroblast growth factor 23
Phosphaturic mesenchymal tumours secrete FGF23, which inhibits renal phosphate reabsorption and 1-alpha-hydroxylase. The result is hypophosphataemic osteomalacia that is cured by removing the tumour.
Option by option
A. Fibroblast growth factor 23 (correct)
Correct. Tumour-derived FGF23 causes phosphate wasting and low calcitriol.
B. Sclerostin
Sclerostin inhibits bone formation and does not cause renal phosphate loss.
C. Interleukin-6
Interleukin-6 is involved in inflammation and myeloma bone disease and does not cause phosphate wasting.
D. Parathyroid hormone-related peptide
PTHrP causes hypercalcaemia of malignancy, not hypophosphataemic osteomalacia.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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