{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,16]],"date-time":"2026-05-16T00:17:51Z","timestamp":1778890671657,"version":"3.51.4"},"reference-count":30,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["SPI"],"published-print":{"date-parts":[[2009,4]]},"abstract":"<jats:p>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.<\/jats:p>","DOI":"10.3171\/2009.1.spine08351","type":"journal-article","created":{"date-parts":[[2009,5,15]],"date-time":"2009-05-15T00:22:15Z","timestamp":1242346935000},"page":"329-333","source":"Crossref","is-referenced-by-count":22,"title":["Oncogenic osteomalacia caused by a phosphaturic mesenchymal tumor of the thoracic spine"],"prefix":"10.3171","volume":"10","author":[{"given":"Elena","family":"Pirola","sequence":"first","affiliation":[{"name":"Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francesco","family":"Vergani","sequence":"additional","affiliation":[{"name":"Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paolo","family":"Casiraghi","sequence":"additional","affiliation":[{"name":"Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eugenio Biagio","family":"Leone","sequence":"additional","affiliation":[{"name":"Pathology Departments, University of Milano-Bicocca, Monza, Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paolo","family":"Guerra","sequence":"additional","affiliation":[{"name":"Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Erik Pietro","family":"Sganzerla","sequence":"additional","affiliation":[{"name":"Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1754","reference":[{"key":"b1-0100329","series-title":"Ital J Orthop Traumatol","first-page":"379","article-title":"Osteoblastoma associated with osteomalacia (presentation of a case and review of the literature)","volume":"4","author":"Boriani","year":"1978"},{"key":"b2-0100329","series-title":"Pediatr Clin North Am","doi-asserted-by":"publisher","first-page":"443","DOI":"10.1016\/S0031-3955(05)70485-5","article-title":"New prospectives on the biology and treatment of X-linked hpophosphatemic rickets","volume":"44","author":"Carpenter","year":"1997"},{"key":"b3-0100329","series-title":"N Engl J Med","doi-asserted-by":"publisher","first-page":"1705","DOI":"10.1056\/NEJMe030037","article-title":"Oncogenic osteomalacia, a complex dance of factors","volume":"348","author":"Carpenter","year":"2003"},{"key":"b4-0100329","series-title":"Rheumatology","doi-asserted-by":"publisher","first-page":"1415","DOI":"10.1093\/rheumatology\/39.12.1415","article-title":"Four cases of acquired hypophosphataemic (\u2018oncogenic\u2019) osteomalacia. 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