Troude Lucas, Melot Anthony, Brunel Hervé, Roche Pierre-Hugues
Department of Neurosurgery, CHU Nord, Marseille, France.
J Neurosurg. 2016 Jun;124(6):1712-5. doi: 10.3171/2015.3.JNS142446. Epub 2015 Oct 23.
Arteriovenous malformations (AVMs) of the spine display a variety of different locations, angioarchitectures, and clinical presentations. The authors describe an exceptional case of a filum terminale AVM that is not described in any classification and discuss the origin and management of this malformation. A 59-year-old woman was admitted in June 2012 for cauda equina syndrome. Magnetic resonance imaging and spinal angiography revealed an AVM of the filum terminale, located below the conus medullaris, fed by the anterior spinal artery. After an unsuccessful attempt to reach the nidus with a microcatheter, the AVM was resected. At 20 months after surgery, the patient was fully independent and radiological images confirmed the exclusion of the malformation. AVMs that originate from the filum terminale are exceptional. According to updated classifications, AVMs of the filum terminale should be categorized as a separate entity.
脊柱动静脉畸形(AVM)表现出多种不同的位置、血管构筑和临床表现。作者描述了一例终丝AVM的特殊病例,该病例在任何分类中均未被描述,并讨论了这种畸形的起源和治疗方法。一名59岁女性于2012年6月因马尾综合征入院。磁共振成像和脊髓血管造影显示终丝AVM,位于脊髓圆锥下方,由脊髓前动脉供血。在尝试用微导管到达病灶未成功后,切除了该AVM。术后20个月,患者完全独立,影像学检查证实畸形已被排除。起源于终丝的AVM很罕见。根据最新分类,终丝AVM应归类为一个单独的实体。