Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour

Oncogenic osteomalacia is a rare metabolic bone disease characterized by phosphate leakage from the kidney and subsequent hypophosphatemia. It is caused by a phosphaturic factor produced by certain tumours. Removal of such tumours can completely cure the condition. Here, we report the case of a pati...

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Autores principales: Radaideh, A.R.M., Jaradat, D., Abu-Kalaf, M.M., Nusier‡, M.K.
Formato: Texto
Lenguaje:English
Publicado: Multimed Inc. 2009
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768508/
https://www.ncbi.nlm.nih.gov/pubmed/19862367
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author Radaideh, A.R.M.
Jaradat, D.
Abu-Kalaf, M.M.
Nusier‡, M.K.
author_facet Radaideh, A.R.M.
Jaradat, D.
Abu-Kalaf, M.M.
Nusier‡, M.K.
author_sort Radaideh, A.R.M.
collection PubMed
description Oncogenic osteomalacia is a rare metabolic bone disease characterized by phosphate leakage from the kidney and subsequent hypophosphatemia. It is caused by a phosphaturic factor produced by certain tumours. Removal of such tumours can completely cure the condition. Here, we report the case of a patient who was crippled with oncogenic osteomalacia. Extensive study revealed a tumour deeply located in the pelvis; removal of the tumour resulted in complete recovery. The tumour was identified as a mesenchymal tumour (mixed connective-tissue variant). The diagnostic evaluation, differential diagnosis, and treatment are discussed.
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spelling pubmed-27685082009-10-27 Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour Radaideh, A.R.M. Jaradat, D. Abu-Kalaf, M.M. Nusier‡, M.K. Curr Oncol Case Report Oncogenic osteomalacia is a rare metabolic bone disease characterized by phosphate leakage from the kidney and subsequent hypophosphatemia. It is caused by a phosphaturic factor produced by certain tumours. Removal of such tumours can completely cure the condition. Here, we report the case of a patient who was crippled with oncogenic osteomalacia. Extensive study revealed a tumour deeply located in the pelvis; removal of the tumour resulted in complete recovery. The tumour was identified as a mesenchymal tumour (mixed connective-tissue variant). The diagnostic evaluation, differential diagnosis, and treatment are discussed. Multimed Inc. 2009-09 /pmc/articles/PMC2768508/ /pubmed/19862367 Text en 2009 Multimed Inc. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Radaideh, A.R.M.
Jaradat, D.
Abu-Kalaf, M.M.
Nusier‡, M.K.
Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour
title Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour
title_full Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour
title_fullStr Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour
title_full_unstemmed Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour
title_short Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour
title_sort resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768508/
https://www.ncbi.nlm.nih.gov/pubmed/19862367
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