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Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot

dc.contributor.authorCorreia, J
dc.contributor.authorMachado, M
dc.contributor.authorGonçalves, R
dc.contributor.authorJonge, F
dc.contributor.authorMicaelo, M
dc.contributor.authorPedrosa, C
dc.contributor.authorPortela, J
dc.date.accessioned2022-06-15T14:05:18Z
dc.date.available2022-06-15T14:05:18Z
dc.date.issued2021
dc.description.abstractPhosphaturic mesenchymal tumors are the main cause of tumor-induced osteomalacia, a distinctive paraneoplastic syndrome mediated by overproduction of fibroblast growth factor 23, that leads to renal phosphate wasting and hypophosphatemia. Diagnosis of this mesenchymal tumors is difficult and usually delayed for several years. We present the case of a 70-years-old-male with generalized bone pain, multiple pathological fractures and persistent hypophosphatemia, diagnosed with tumor-induced osteomalacia after 4 years of the onset of symptoms. The tumor was localized in the forefoot using Gallium 68-DOTANOC positron emission tomography-computed tomography and successfully surgically treated. This case report highlights the importance of recognizing these rare tumors, as early diagnosis can prevent long-term morbidity.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationRadiol Case Rep. 2021 Apr 9;16(6):1355-1362.pt_PT
dc.identifier.doi10.1016/j.radcr.2021.03.015.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4116
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.subjectHCC ORTpt_PT
dc.subjectPhosphaturic Mesenchymal Tumorspt_PT
dc.subjectTumor-Induced Osteomalaciapt_PT
dc.subjectFibroblast Growth Factor 23pt_PT
dc.subjectHypophosphatemiapt_PT
dc.titleDelayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Footpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage1362pt_PT
oaire.citation.startPage1355pt_PT
oaire.citation.titleRadiology Case Reportspt_PT
oaire.citation.volume16pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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