Ciappetta P, Occhiogrosso G, Domenicucci M, D'Andrea G, Bastianello S, Frati A
Department of Neurosurgery, University of Bari, Bari, Italy.
J Exp Clin Cancer Res. 2007 Jun;26(2):281-5.
Hemangioblastomas of the filum terminale are particularly rare tumors. The authors present the case of a 62-year-old woman with a 6 month history of low-back-pain, who underwent surgery for the removal of an hemangioblastoma affecting the cauda at L2-L3 level. This highly vascularized tumour is tightly adherent to the filum terminale and hence is a very challenging pathology to remove. Histologically it consisted in vascular structures interposed to a network of capillary-like vessels, surrounded by stromal cells. MRI, angiography with pre-surgical embolization, and radical surgery represent the focal points in the diagnosis and treatment of these tumours. The most relevant literature has been carefully reviewed.
终丝血管母细胞瘤是极为罕见的肿瘤。作者报告了一例62岁女性病例,该患者有6个月的腰痛病史,因L2 - L3水平马尾处的血管母细胞瘤接受手术切除。这种高度血管化的肿瘤与终丝紧密粘连,因此是一种极具挑战性的需切除病理病变。组织学上,它由插入毛细血管样血管网络中的血管结构组成,周围环绕着基质细胞。MRI、术前栓塞血管造影和根治性手术是这些肿瘤诊断和治疗的重点。作者已仔细查阅了最相关的文献。