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Tumor-induced hypophosphatemia

Significant hypophosphatemia is commonly due to Vitamin D deficiency. Any sporadic onset of hypophosphatemia in adults warrants workup to identify alternate causes. Hypophosphatemia may also be the only manifestation of an occult malignancy. A high index of clinical suspicion can help diagnose such...

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Detalles Bibliográficos
Autores principales: Mulani, M., Somani, K., Bichu, S., Billa, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255994/
https://www.ncbi.nlm.nih.gov/pubmed/28182049
http://dx.doi.org/10.4103/0971-4065.179302
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author Mulani, M.
Somani, K.
Bichu, S.
Billa, V.
author_facet Mulani, M.
Somani, K.
Bichu, S.
Billa, V.
author_sort Mulani, M.
collection PubMed
description Significant hypophosphatemia is commonly due to Vitamin D deficiency. Any sporadic onset of hypophosphatemia in adults warrants workup to identify alternate causes. Hypophosphatemia may also be the only manifestation of an occult malignancy. A high index of clinical suspicion can help diagnose such conditions in early stages. Prompt treatment of the cause can correct this biochemical abnormality. We describe a case report of a woman presenting with severe hypophosphatemia and osteomalacia, leading eventually to the diagnosis of a phosphaturic mesenchymal tumor of the temporo-occipital bone. Surgical resection of tumor led to normalization of the biochemical parameters as well as a complete clinical recovery.
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spelling pubmed-52559942017-02-08 Tumor-induced hypophosphatemia Mulani, M. Somani, K. Bichu, S. Billa, V. Indian J Nephrol Case Report Significant hypophosphatemia is commonly due to Vitamin D deficiency. Any sporadic onset of hypophosphatemia in adults warrants workup to identify alternate causes. Hypophosphatemia may also be the only manifestation of an occult malignancy. A high index of clinical suspicion can help diagnose such conditions in early stages. Prompt treatment of the cause can correct this biochemical abnormality. We describe a case report of a woman presenting with severe hypophosphatemia and osteomalacia, leading eventually to the diagnosis of a phosphaturic mesenchymal tumor of the temporo-occipital bone. Surgical resection of tumor led to normalization of the biochemical parameters as well as a complete clinical recovery. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5255994/ /pubmed/28182049 http://dx.doi.org/10.4103/0971-4065.179302 Text en Copyright: © 2017 Indian Journal of Nephrology 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Mulani, M.
Somani, K.
Bichu, S.
Billa, V.
Tumor-induced hypophosphatemia
title Tumor-induced hypophosphatemia
title_full Tumor-induced hypophosphatemia
title_fullStr Tumor-induced hypophosphatemia
title_full_unstemmed Tumor-induced hypophosphatemia
title_short Tumor-induced hypophosphatemia
title_sort tumor-induced hypophosphatemia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255994/
https://www.ncbi.nlm.nih.gov/pubmed/28182049
http://dx.doi.org/10.4103/0971-4065.179302
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