Roncaroli F, Scheithauer B W, Papazoglou S
Department of Oncology, Bellaria Hospital, Bologna, Italy
J Neurosurg. 2001 Jul;95(1 Suppl):93-5. doi: 10.3171/spi.2001.95.1.0093.
A case of polymorphous hemangioendothelioma of the spinal cord is described. This 55-year-old woman presented with an 18-month history of lower-extremity sensorimotor deficit. A magnetic resonance image revealed an enhancing, intradural, extramedullary nodule at the T 1-2 level. On gross inspection, the lesion measured 3.5 cm and was firmly attached to spinal cord parenchyma and adjacent nerve roots. It was completely removed. Fourteen months after surgery the patient's neurological deficit had resolved. Polymorphous hemangioendothelioma is a rare vascular tumor of borderline malignancy. Most occur in lymph nodes. None has been reported to occur in the central and peripheral nervous system. Based on current experience, resection and close follow up seems the best therapeutic approach.
本文描述了一例脊髓多形性血管内皮瘤病例。该55岁女性有18个月的下肢感觉运动功能障碍病史。磁共振成像显示T1-2水平有一个强化的硬膜内髓外结节。大体检查时,病变大小为3.5 cm,与脊髓实质和相邻神经根紧密相连。病变被完全切除。术后14个月,患者的神经功能缺损已消失。多形性血管内皮瘤是一种罕见的交界性恶性血管肿瘤。大多数发生在淋巴结。尚无发生于中枢和周围神经系统的报道。根据目前的经验,手术切除并密切随访似乎是最佳的治疗方法。