Department of Neurosurgery, Akdeniz University School of Medicine, 07070/KonyaaltI/Antalya/Turkey.
Neurol Neurochir Pol. 2012 Sep-Oct;46(5):496-500. doi: 10.5114/ninp.2012.31362.
Klippel-Trenaunay-Weber syndrome (KTWS) is a rare, congenital vascular disorder characterized by cutaneous haemangiomas, venous varicosities, and hypertrophy of the osseous and soft tissue. Various vascular anomalies of the central nervous system have been described in this syndrome. Two previous associations between KTWS and spinal cord cavernous malformations have been reported in the English literature. In this report, we present a patient in whom multiple cavernous malformations located in the conus medullaris region and cauda equina were associated with KTWS. General physical examination as well as neuroradiological and operative findings are described.
Klippel-Trenaunay-Weber 综合征(KTWS)是一种罕见的先天性血管疾病,其特征为皮肤血管瘤、静脉瘤和骨与软组织的肥大。该综合征中已有多种中枢神经系统血管异常的描述。在英文文献中,已有两次 KTWS 与脊髓海绵状血管畸形相关的报道。在此报告中,我们介绍了一位患者,其在脊髓圆锥区和马尾处存在多个海绵状血管畸形,同时患有 KTWS。描述了一般体格检查以及神经放射学和手术结果。