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

Internet

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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