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Oncogenic osteomalacia diagnosed by blood pool scintigraphy

Oncogenic osteomalacia is a rare metabolic bone disease characterized by phosphaturia and hypophosphatemia. Certain tumors secrete a phosphaturic factor, which results in this metabolic abnormality; this factor called as phosphatonin, is in fact a fibroblast growth factor 23 (FGF-23) involved closel...

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Autores principales: Palaniswamy, Shanmuga Sundaram, Subramanyam, Padma, Kumar, Harish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613625/
https://www.ncbi.nlm.nih.gov/pubmed/23559714
http://dx.doi.org/10.4103/0972-3919.106702
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author Palaniswamy, Shanmuga Sundaram
Subramanyam, Padma
Kumar, Harish
author_facet Palaniswamy, Shanmuga Sundaram
Subramanyam, Padma
Kumar, Harish
author_sort Palaniswamy, Shanmuga Sundaram
collection PubMed
description Oncogenic osteomalacia is a rare metabolic bone disease characterized by phosphaturia and hypophosphatemia. Certain tumors secrete a phosphaturic factor, which results in this metabolic abnormality; this factor called as phosphatonin, is in fact a fibroblast growth factor 23 (FGF-23) involved closely in phosphate homeostasis and skeletogenesis. Complete excision of these tumors facilitates reversal of the problem. We have reported here the case of a patient who was crippled with this disease and on thorough investigation revealed an oncogenic osteomalacia with tumor focus in the right tibia. The tumor was identified as a mesenchymal tumor, i.e., hemangiopericytoma. Tumor excision alleviated patient symptoms with rapid symptomatic and biochemical improvement.
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spelling pubmed-36136252013-04-04 Oncogenic osteomalacia diagnosed by blood pool scintigraphy Palaniswamy, Shanmuga Sundaram Subramanyam, Padma Kumar, Harish Indian J Nucl Med Case Report Oncogenic osteomalacia is a rare metabolic bone disease characterized by phosphaturia and hypophosphatemia. Certain tumors secrete a phosphaturic factor, which results in this metabolic abnormality; this factor called as phosphatonin, is in fact a fibroblast growth factor 23 (FGF-23) involved closely in phosphate homeostasis and skeletogenesis. Complete excision of these tumors facilitates reversal of the problem. We have reported here the case of a patient who was crippled with this disease and on thorough investigation revealed an oncogenic osteomalacia with tumor focus in the right tibia. The tumor was identified as a mesenchymal tumor, i.e., hemangiopericytoma. Tumor excision alleviated patient symptoms with rapid symptomatic and biochemical improvement. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3613625/ /pubmed/23559714 http://dx.doi.org/10.4103/0972-3919.106702 Text en Copyright: © Indian Journal of Nuclear Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Palaniswamy, Shanmuga Sundaram
Subramanyam, Padma
Kumar, Harish
Oncogenic osteomalacia diagnosed by blood pool scintigraphy
title Oncogenic osteomalacia diagnosed by blood pool scintigraphy
title_full Oncogenic osteomalacia diagnosed by blood pool scintigraphy
title_fullStr Oncogenic osteomalacia diagnosed by blood pool scintigraphy
title_full_unstemmed Oncogenic osteomalacia diagnosed by blood pool scintigraphy
title_short Oncogenic osteomalacia diagnosed by blood pool scintigraphy
title_sort oncogenic osteomalacia diagnosed by blood pool scintigraphy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613625/
https://www.ncbi.nlm.nih.gov/pubmed/23559714
http://dx.doi.org/10.4103/0972-3919.106702
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