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Phosphaturic Mesenchymal Tumor.

Authors :
Benson JC
Trejo-Lopez JA
Nassiri AM
Eschbacher K
Link MJ
Driscoll CL
Tiegs RD
Sfeir J
DeLone DR
Source :
AJNR. American journal of neuroradiology [AJNR Am J Neuroradiol] 2022 Jun; Vol. 43 (6), pp. 817-822. Date of Electronic Publication: 2022 May 19.
Publication Year :
2022

Abstract

Phosphaturic mesenchymal tumors (PMTs) are neoplasms associated with tumor-induced osteomalacia. Patients typically present with pathologic fractures in the setting of chronic hypophosphatemic hyperphosphaturic osteomalacia, as well as gradual muscle weakness, bone pain, and difficulty walking. Because of their rarity and nonspecific symptomatology, phosphaturic mesenchymal tumors often go undiagnosed for years. Even when discovered on imaging, the tumors can be diagnostically challenging for radiologists. Phosphaturic mesenchymal tumors often tend to be small and can be located nearly anywhere in the body, and, therefore, can mimic many other tumors. This case highlights the imaging and pathologic markers of a phosphaturic mesenchymal tumor, often found in a patient with tumor-induced osteomalacia.<br /> (© 2022 by American Journal of Neuroradiology.)

Details

Language :
English
ISSN :
1936-959X
Volume :
43
Issue :
6
Database :
MEDLINE
Journal :
AJNR. American journal of neuroradiology
Publication Type :
Academic Journal
Accession number :
35589138
Full Text :
https://doi.org/10.3174/ajnr.A7513