Gläsker S, Klingler J H, Müller K, Würtenberger C, Hader C, Zentner J, Neumann H P H, Velthoven V Van
Department of Neurosurgery, Freiburg University Medical Center, Freiburg, Germany.
Cent Eur Neurosurg. 2010 May;71(2):80-7. doi: 10.1055/s-0029-1234040. Epub 2010 Mar 12.
Hemangioblastomas are rare CNS tumors, which are mostly located in the posterior fossa or spinal cord and occasionally in spinal nerves. They can occur sporadically or as a component tumor of von Hippel-Lindau (VHL) disease, an autosomal dominant tumor syndrome. The limited awareness of several pitfalls in the therapy of these rare lesions results in delayed or suboptimal treatment for many of these patients, especially those with VHL disease. The University of Freiburg serves as a reference center for patients with VHL disease and hemangioblastomas. The current therapeutic strategies for hemangioblastoma patients and typical pitfalls are presented here.
血管母细胞瘤是罕见的中枢神经系统肿瘤,大多位于后颅窝或脊髓,偶尔也见于脊神经。它们可散发性发生,或作为常染色体显性肿瘤综合征——冯·希佩尔-林道(VHL)病的组成肿瘤出现。对这些罕见病变治疗中一些陷阱的认识不足,导致许多此类患者,尤其是患有VHL病的患者,治疗延迟或未达最佳效果。弗莱堡大学是VHL病和血管母细胞瘤患者的参考中心。本文介绍了血管母细胞瘤患者目前的治疗策略及典型陷阱。