Sandhu F A, Martuza R L
Georgetown University Medical Center, Department of Neurosurgery, Washington, DC, USA.
J Neurooncol. 2000;46(3):241-7. doi: 10.1023/a:1006352106762.
A craniofacial hemangiopericytoma associated with oncogenic osteomalacia is described and the literature is reviewed. A 46 year-old male with multiple fractures and hypophosphatemia was found to have a craniofacial mass extending from the right ethmoid sinus into the right frontal lobe. Initial detection of the tumor was made with an 111Indium-pentreotide scan (Octreoscan). Gross total resection of the tumor was achieved and the patient received postoperative radiation therapy. One year after surgery, the patient remains free of tumor with significant increase in bone density and normal phosphate levels. This is the first report of a hemangiopericytoma invading the brain that was associated with paraneoplastic hypophosphatemia and osteomalacia. Also, this is the first reported detection of a hemangiopericytoma by an Octreoscan. Primary detection and secondary surveillance of hemangiopericytomas may be possible with serial Octreoscans.
本文描述了一例与致癌性骨软化症相关的颅面血管外皮细胞瘤,并对相关文献进行了综述。一名46岁男性,有多处骨折和低磷血症,发现有一个颅面肿物,从右侧筛窦延伸至右侧额叶。最初通过铟-111喷曲肽扫描(奥曲肽扫描)发现该肿瘤。肿瘤实现了大体全切,患者接受了术后放疗。术后一年,患者无肿瘤复发,骨密度显著增加,磷酸盐水平正常。这是首例侵犯脑部的血管外皮细胞瘤与副肿瘤性低磷血症和骨软化症相关的报告。此外,这也是首次通过奥曲肽扫描检测到血管外皮细胞瘤。通过连续的奥曲肽扫描,可能实现血管外皮细胞瘤的初诊和二次监测。