Suppr超能文献

上颌窦间叶性磷酸盐尿性肿瘤:一例报告。

Mesenchymal phosphaturic neoplasm in the maxillary sinus: a case report.

机构信息

Department of Maxillo-Facial Surgery, San Paolo Hospital, University of Milan, Via A. Di Rudinì 8, Milan, Italy.

出版信息

Int J Oral Maxillofac Surg. 2010 Oct;39(10):1027-32. doi: 10.1016/j.ijom.2010.04.039. Epub 2010 May 21.

Abstract

The authors describe a case of oncogenic osteomalacia due to a mesenchymal phosphaturic tumour in the maxillary sinus. This is a paraneoplastic syndrome in which a tumour produces a peptide hormone-like substance (phosphatonin) that causes a urinary loss of phosphates resulting in a debilitating systemic condition. In this case, the patient experienced muscle stiffness, reduction of muscle tone, loss of weight and pathological fractures. Clinical and radiological examination revealed a tumour in the right maxillary sinus; all other results were negative. The diagnosis following pathology examination was mesenchymal phosphaturic tumour with a haemangiopericytoma-like vascular pattern. Different histological types of mesenchymal tumours can be associated with paraneoplastic syndrome, but their localization in the paranasal sinuses is rare. The correct diagnosis allows the appropriate therapeutic approach, which can lead to an almost immediate resolution of the clinical situation after surgical removal of the neoplasm as in the present case. Oncogenic osteomalacia is rare, particularly in the maxillofacial region, and only a few cases have been reported.

摘要

作者描述了一例发生于上颌窦间叶磷酸盐尿肿瘤的癌源性骨软化症。这是一种副瘤综合征,其中肿瘤产生一种肽激素样物质(磷酸激素),导致磷酸盐尿丢失,从而导致衰弱的全身状况。在这种情况下,患者出现肌肉僵硬、肌肉张力降低、体重减轻和病理性骨折。临床和放射学检查显示右侧上颌窦有肿瘤;其他所有结果均为阴性。病理检查诊断为间叶磷酸盐尿肿瘤,具有血管外皮细胞瘤样血管模式。不同组织学类型的间叶肿瘤可与副瘤综合征相关,但它们在上颌窦内的定位较为罕见。正确的诊断可采用适当的治疗方法,在本病例中,通过手术切除肿瘤后,几乎可立即缓解临床状况。癌源性骨软化症较为罕见,特别是在颌面区域,仅有少数病例报道。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验