Åpne denne publikasjonen i ny fane eller vindu >>Vise andre…
2008 (engelsk)Inngår i: Endocrine Practice, ISSN 1530-891X, E-ISSN 1934-2403, Vol. 14, nr 3, s. 362-367Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]
Objective: To report on a novel strategy for tumor localization in a 62-year-old man with hypophosphatemic tumor-induced osteomalacia (TIO).
Methods: Repeated computed tomographic and magnetic resonance imaging scans failed to localize any tumor in a patient with adult-onset hypophosphatemic osteomalacia. Therefore, venous sampling for fibroblast growth factor-23 (FGF23)—a circulating hormone that has been identified as a causative factor for TIO—in major veins was conducted. Serum FGF23 was measured from collected samples by an intact FGF23 enzyme-linked immunosorbent assay.
Results: Venous sampling suggested a local increase in serum FGF23 in the left femoral vein; this finding prompted performance of octreotide scintigraphy restricted to the left leg. A tumor was located at the lateral condyle of the left femur, which was also confirmed by magnetic resonance imaging. Surgical resection of the tumor normalized the serum phosphorus and 1,25-dihydroxyvitamin D3 levels within 5 to 10 days, and FGF23 declined to normal levels within 24 hours. Histologic analysis supported the diagnosis of a soft-tissue giant cell tumor.
Conclusion: Our study case demonstrates the diagnostic complexity and difficulties in localizing a small tumor in a patient with TIO. Venous sampling for FGF23 may be helpful in tumor localization in sporadic cases of hypophosphatemic osteomalacia, especially when noninvasive diagnostic techniques prove insufficient.
HSV kategori
Identifikatorer
urn:nbn:se:liu:diva-53714 (URN)10.4158/EP.14.3.362 (DOI)18463045 (PubMedID)
2010-02-012010-02-012017-12-12