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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
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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. |
format | Online Article Text |
id | pubmed-3613625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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