Spinal dural arteriovenous fistula: a comprehensive review of the history, classification systems, management, and prognosis.

Ali Alkhaibary, Ahoud Alharbi, Nada Alnefaie, Hajar Alammar, Alshaymaa M Arishy, Noor Alghanim, Yazeed M Aldhfyan, Arwa Albaiahy, Yahya H Khormi, Wael Alshaya, Saad AlQahatani, Ahmed Aloraidi, Ahmed Alkhani, Sami Khairy
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Abstract

Spinal dural arteriovenous fistulas account for the majority of spinal vascular malformations. They are typically located in the thoracolumbar region and are diagnosed in the middle-aged and elderly populations. Although spinal dural arteriovenous fistulas have been postulated to be acquired, their exact development remains uncertain. Typically, the arteriovenous shunt is situated close to the spinal nerve root, inside the dura mater, where the blood from the radiculomeningeal artery and radicular vein intermix. Throughout history, there have been multiple classification systems of spinal arteriovenous shunts since 1967. Those were mainly based on the evolution of diagnostic studies as well as the treatment of these lesions. Such classification systems have undergone significant changes over the years. Unlike intracranial dural arteriovenous fistula, spinal dural arteriovenous fistula is progressive in nature. The neurological manifestations, due to venous congestion, tend to be insidious as well as non-specific. These include sensory deficits, such as paresthesia, bilateral and/or unilateral radicular pain affecting the lower limbs, and gait disturbances. Spinal dural arteriovenous fistulas can be suspected on magnetic resonance imaging/magnetic resonance angiography and confirmed by digital subtraction angiography (DSA). The management includes surgery, endovascular therapy, and in selected cases, radiotherapy. The treatment goal of spinal dural arteriovenous fistula is to halt the progression of the disease. The prognosis depends on both the duration of symptoms as well as the clinical condition prior to therapy. The present article comprehensively reviews the pathophysiology, changes in classification systems, natural history, clinical manifestations, radiological features, management, and prognosis.

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脊髓硬膜动静脉瘘:病史、分类系统、管理和预后的全面回顾。
脊髓硬膜动静脉瘘占脊髓血管畸形的大多数。脊髓硬膜动静脉瘘通常位于胸腰部,多见于中老年人群。虽然脊髓硬膜动静脉瘘被推测是后天形成的,但其确切的发展过程仍不确定。通常情况下,动静脉分流口位于靠近脊神经根的硬脑膜内,来自脊髓动静脉和根静脉的血液在此交汇。纵观历史,自 1967 年以来,脊髓动静脉分流有多种分类系统。这些系统主要基于诊断研究的发展以及对这些病变的治疗。多年来,这些分类系统发生了重大变化。与颅内硬脑膜动静脉瘘不同,脊髓硬脑膜动静脉瘘是渐进性的。静脉充血导致的神经系统表现往往是隐匿性和非特异性的。这些表现包括感觉障碍,如麻痹、影响下肢的双侧和/或单侧根性疼痛以及步态障碍。磁共振成像/磁共振血管造影可怀疑脊髓硬膜动静脉瘘,数字减影血管造影(DSA)可确诊脊髓硬膜动静脉瘘。治疗方法包括手术、血管内治疗,部分病例可采用放射治疗。脊髓硬膜动静脉瘘的治疗目标是阻止病情发展。预后取决于症状持续时间以及治疗前的临床状况。本文全面回顾了该病的病理生理学、分类系统的变化、自然史、临床表现、放射学特征、治疗和预后。
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CiteScore
2.70
自引率
0.00%
发文量
224
审稿时长
10 weeks
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