| Literature DB >> 19441990 |
Elena Pirola1, Francesco Vergani, Paolo Casiraghi, Eugenio Biagio Leone, Paolo Guerra, Erik Pietro Sganzerla.
Abstract
Phosphaturic mesenchymal tumors that cause the paraneoplastic syndrome known as oncogenic osteomalacia are rare. The authors report on the case of a 57-year-old man with a history of osteomalacia and in whom was diagnosed a thoracic spine tumor at the T-4 level. Complete tumor resection was accomplished. The histological diagnosis was phosphaturic mesenchymal tumor (mixed connective tissue variant). After lesion removal, the paraneoplastic syndrome resolved. At the 24-month follow-up, no recurrence of the disease was observed. The clinical presentation, surgical technique, and follow-up in this case were reviewed in detail.Entities:
Mesh:
Year: 2009 PMID: 19441990 DOI: 10.3171/2009.1.SPINE08351
Source DB: PubMed Journal: J Neurosurg Spine ISSN: 1547-5646