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深度软组织肿瘤切除术后严重成骨性低血磷性骨软化症的缓解。

Resolution of severe oncogenic hypophosphatemic osteomalacia after resection of a deeply located soft-tissue tumour.

机构信息

Departments of Medicine, Prince Basma Teaching Hospital, Ministry of Health, Irbid, Jordan.

出版信息

Curr Oncol. 2009 Sep;16(5):87-90. doi: 10.3747/co.v16i5.412.

Abstract

Oncogenic osteomalacia is a rare metabolic bone disease characterized by phosphate leakage from the kidney and subsequent hypophosphatemia. It is caused by a phosphaturic factor produced by certain tumours. Removal of such tumours can completely cure the condition. Here, we report the case of a patient who was crippled with oncogenic osteomalacia. Extensive study revealed a tumour deeply located in the pelvis; removal of the tumour resulted in complete recovery. The tumour was identified as a mesenchymal tumour (mixed connective-tissue variant). The diagnostic evaluation, differential diagnosis, and treatment are discussed.

摘要

成骨性骨软化症是一种罕见的代谢性骨病,其特征为肾脏磷渗漏和随后的低磷血症。它是由某些肿瘤产生的一种排磷因子引起的。切除这些肿瘤可以完全治愈这种疾病。在这里,我们报告了一例患有成骨性骨软化症的患者。广泛的研究显示肿瘤深位于骨盆;切除肿瘤导致完全恢复。肿瘤被确定为间叶肿瘤(混合结缔组织变异型)。讨论了诊断评估、鉴别诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db4b/2768508/639d14d6b6f2/co16-5-87f1.jpg

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