Statistics from Altmetric.com
Phosphaturic mesenchymal tumour (PMT) is a rare mesenchymal tumour, which most often occurs in middle-aged adults, either in soft tissue or bone.1 ,2 PMTs are variable in their histomorphological appearance but often show a mixture of bland spindle cells embedded in a highly vascular (hemangiopericytoma-like) myxochondroid matrix, mature fat and osteoclast-like giant cells (figure 1A, B). The differential diagnosis of PMT is broad. In most cases of PMT, the patient has a longstanding clinical history of osteomalacia, facilitating the diagnosis of PMT. However, unsuspected PMT may be histomorphologically confused with other giant cell containing bone tumours, including chondromyxoid fibromas and chondroblastomas. Recognition of the distinctive ‘grungy’-appearing calcified matrix is the best way to distinguish PMT from other tumours (figure 1B). Detection of Fibroblast Growth Factor (FGF23) expression is …
Contributors DC conceived and designed the study. The manuscript was written by DC and JVD. Review of slides was undertaken by DC and JVD. All authors have read and approved the final manuscript.
Competing interests None declared.
Ethics approval This study has been performed according to the guidelines of the local ethics committee (Ghent University Hospital).
Provenance and peer review Not commissioned; externally peer reviewed.
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.