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胸椎磷酸尿性间叶肿瘤所致的致癌性骨软化症。

Oncogenic osteomalacia caused by a phosphaturic mesenchymal tumor of the thoracic spine.

作者信息

Pirola Elena, Vergani Francesco, Casiraghi Paolo, Leone Eugenio Biagio, Guerra Paolo, Sganzerla Erik Pietro

机构信息

Neurosurgery, University of Milano-Bicocca, Monza, Italy.

出版信息

J Neurosurg Spine. 2009 Apr;10(4):329-33. doi: 10.3171/2009.1.SPINE08351.

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.

摘要

导致副肿瘤综合征(即致癌性骨软化症)的磷尿性间质性肿瘤很罕见。作者报告了一例57岁男性病例,该患者有骨软化症病史,被诊断为T4水平的胸椎肿瘤。肿瘤被完整切除。组织学诊断为磷尿性间质性肿瘤(混合结缔组织变体)。病变切除后,副肿瘤综合征得以缓解。在24个月的随访中,未观察到疾病复发。本文详细回顾了该病例的临床表现、手术技术及随访情况。

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