Essentials and pitfalls in the treatment of CNS hemangioblastomas and von Hippel-Lindau disease.

Central European Neurosurgery Pub Date : 2010-05-01 Epub Date: 2010-03-12 DOI:10.1055/s-0029-1234040
S Gläsker, J H Klingler, K Müller, C Würtenberger, C Hader, J Zentner, H P H Neumann, V Van Velthoven
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引用次数: 21

Abstract

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.

中枢神经系统血管母细胞瘤和von Hippel-Lindau病治疗的要点和缺陷。
血管母细胞瘤是一种罕见的中枢神经系统肿瘤,多发生于后窝或脊髓,偶有发生于脊神经。它们可以零星发生或作为von Hippel-Lindau (VHL)病(一种常染色体显性肿瘤综合征)的组成部分肿瘤。对这些罕见病变治疗中几个缺陷的认识有限,导致许多患者治疗延迟或治疗次优,特别是那些患有VHL疾病的患者。弗莱堡大学作为VHL疾病和血管母细胞瘤患者的参考中心。血管母细胞瘤患者目前的治疗策略和典型的陷阱在这里提出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Central European Neurosurgery
Central European Neurosurgery CLINICAL NEUROLOGY-NEUROSCIENCES
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