Advanced tumour-induced osteomalacia secondary to sinonasal phosphaturic mesenchymal tumour

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dc.contributor.authorvan Wijk, Monica
dc.contributor.authorOpperman, Johan F.
dc.contributor.authorAfrogheh, Amir H.
dc.date.accessioned2024-11-21T10:09:24Z
dc.date.available2024-11-21T10:09:24Z
dc.date.issued2024
dc.description.abstractPhosphaturic mesenchymal tumours (PMT) are rare, benign lesions and the most common tumour to cause tumour-induced osteomalacia (TIO), a paraneoplastic syndrome. Patients frequently exhibit severe osteomalacia, accompanied by multiple fractures, which significantly impair their quality of life. Complete surgical resection is curative. Contribution: A rare case of sinonasal PMT is presented, with a focus on the imaging findings and role of the radiologist and nuclear physician.
dc.identifier.citationVan Wijk, M., van Rensburg, L.J., Berndorfler, B.D., Opperman, J.F., Grobbelaar, J., Afrogheh, A.H., Versveld, S. and Davis, R., 2024. Advanced tumour-induced osteomalacia secondary to sinonasal phosphaturic mesenchymal tumour. SA Journal of Radiology, 28(1), p.2975.
dc.identifier.urihttps://doi.org/10.4102/sajr.v28i1.2975
dc.identifier.urihttps://hdl.handle.net/10566/19707
dc.language.isoen
dc.publisherAOSIS (pty) Ltd
dc.subjectfractures
dc.subjectinduced
dc.subjectmesenchymal
dc.subjectnuclear
dc.subjectosteomalacia
dc.titleAdvanced tumour-induced osteomalacia secondary to sinonasal phosphaturic mesenchymal tumour
dc.typeArticle

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