Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot

Detalhes bibliográficos
Autor(a) principal: Correia, J
Data de Publicação: 2021
Outros Autores: Machado, M, Gonçalves, R, Jonge, F, Micaelo, M, Pedrosa, C, Portela, J
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.17/4116
Resumo: Phosphaturic 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.
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spelling Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the FootHCC ORTPhosphaturic Mesenchymal TumorsTumor-Induced OsteomalaciaFibroblast Growth Factor 23HypophosphatemiaPhosphaturic 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.ElsevierRepositório do Centro Hospitalar Universitário de Lisboa Central, EPECorreia, JMachado, MGonçalves, RJonge, FMicaelo, MPedrosa, CPortela, J2022-06-15T14:05:18Z20212021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/4116engRadiol Case Rep. 2021 Apr 9;16(6):1355-1362.10.1016/j.radcr.2021.03.015.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:45:24Zoai:repositorio.chlc.min-saude.pt:10400.17/4116Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:21:27.510883Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot
title Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot
spellingShingle Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot
Correia, J
HCC ORT
Phosphaturic Mesenchymal Tumors
Tumor-Induced Osteomalacia
Fibroblast Growth Factor 23
Hypophosphatemia
title_short Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot
title_full Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot
title_fullStr Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot
title_full_unstemmed Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot
title_sort Delayed Diagnosis of Occult Phosphaturic Mesenchymal Tumor in the Foot
author Correia, J
author_facet Correia, J
Machado, M
Gonçalves, R
Jonge, F
Micaelo, M
Pedrosa, C
Portela, J
author_role author
author2 Machado, M
Gonçalves, R
Jonge, F
Micaelo, M
Pedrosa, C
Portela, J
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE
dc.contributor.author.fl_str_mv Correia, J
Machado, M
Gonçalves, R
Jonge, F
Micaelo, M
Pedrosa, C
Portela, J
dc.subject.por.fl_str_mv HCC ORT
Phosphaturic Mesenchymal Tumors
Tumor-Induced Osteomalacia
Fibroblast Growth Factor 23
Hypophosphatemia
topic HCC ORT
Phosphaturic Mesenchymal Tumors
Tumor-Induced Osteomalacia
Fibroblast Growth Factor 23
Hypophosphatemia
description Phosphaturic 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.
publishDate 2021
dc.date.none.fl_str_mv 2021
2021-01-01T00:00:00Z
2022-06-15T14:05:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.17/4116
url http://hdl.handle.net/10400.17/4116
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Radiol Case Rep. 2021 Apr 9;16(6):1355-1362.
10.1016/j.radcr.2021.03.015.
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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