| Literature DB >> 20438469 |
Ann E Marshall, Sarah E Martin, Narasimhan P Agaram, Jey-Hsin Chen, Eric M Horn, Annette C Douglas-Akinwande, Eyas M Hattab.
Abstract
Phosphaturic mesenchymal tumor, mixed connective tissue variant (PMT-MCT) is a rare, largely benign, mesenchymal neoplasm almost invariably associated with oncogenic osteomalacia. It is generally found in the soft tissue and bone of the extremities. We report a case of a 61-year-old female with long-standing osteomalacia who was found to have PMT-MCT of the thoracic spine. There have been very few previously reported cases of PMT involving the spinal vertebrae and neuropathologists should be aware of this lesion. Recognition of PMT-MCT is critical for optimal patient care since complete surgical resection without additional therapy is curative.Entities:
Mesh:
Year: 2010 PMID: 20438469 DOI: 10.1111/j.1750-3639.2009.00360.x
Source DB: PubMed Journal: Brain Pathol ISSN: 1015-6305 Impact factor: 6.508