Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity

Phosphaturic mesenchymal tumor (PMT) is a rare entity that presents as a paraneoplastic syndrome that causes tumor-induced osteomalacia (TIO). Most of these cases were located in the extremities. We report a case of a phosphaturic mesenchymal tumor arising in the left upper thigh. The tumor was disc...

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Detalles Bibliográficos
Autores principales: Hudairy, Rawan E, Meliti, Abdelrazak, Mokhtar, Ghadeer, Alanazi, Maram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Pathology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967444/
https://www.ncbi.nlm.nih.gov/pubmed/35386172
http://dx.doi.org/10.7759/cureus.22712
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author Hudairy, Rawan E
Meliti, Abdelrazak
Mokhtar, Ghadeer
Alanazi, Maram
author_facet Hudairy, Rawan E
Meliti, Abdelrazak
Mokhtar, Ghadeer
Alanazi, Maram
author_sort Hudairy, Rawan E
collection PubMed
description Phosphaturic mesenchymal tumor (PMT) is a rare entity that presents as a paraneoplastic syndrome that causes tumor-induced osteomalacia (TIO). Most of these cases were located in the extremities. We report a case of a phosphaturic mesenchymal tumor arising in the left upper thigh. The tumor was discovered during the clinical workup of a patient complaining of osteomalacia symptoms with multiple fractures.
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spelling pubmed-89674442022-04-05 Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity Hudairy, Rawan E Meliti, Abdelrazak Mokhtar, Ghadeer Alanazi, Maram Cureus Pathology Phosphaturic mesenchymal tumor (PMT) is a rare entity that presents as a paraneoplastic syndrome that causes tumor-induced osteomalacia (TIO). Most of these cases were located in the extremities. We report a case of a phosphaturic mesenchymal tumor arising in the left upper thigh. The tumor was discovered during the clinical workup of a patient complaining of osteomalacia symptoms with multiple fractures. Cureus 2022-02-28 /pmc/articles/PMC8967444/ /pubmed/35386172 http://dx.doi.org/10.7759/cureus.22712 Text en Copyright © 2022, Hudairy et al. https://creativecommons.org/licenses/by/3.0/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 author and source are credited.
spellingShingle Pathology
Hudairy, Rawan E
Meliti, Abdelrazak
Mokhtar, Ghadeer
Alanazi, Maram
Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity
title Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity
title_full Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity
title_fullStr Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity
title_full_unstemmed Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity
title_short Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity
title_sort phosphaturic mesenchymal tumor: a case report of a rare entity
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967444/
https://www.ncbi.nlm.nih.gov/pubmed/35386172
http://dx.doi.org/10.7759/cureus.22712
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AT mokhtarghadeer phosphaturicmesenchymaltumoracasereportofarareentity
AT alanazimaram phosphaturicmesenchymaltumoracasereportofarareentity

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