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Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity
Rawan E Hudairy1, Abdelrazak Meliti1, Ghadeer Mokhtar1
1Anatomic Pathology, King Faisal Specialist Hospital and Research Centre, Jeddah, SAU.
Abstract:
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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