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脊髓前动脉综合征

Anterior Spinal Artery Syndrome

作者信息

Sandoval Jose I., De Jesus Orlando

机构信息

Allegheny Health Network, Neurosurgery and Drexel University

University of Puerto Rico, Medical Sciences Campus, Neurosurgery Section

Abstract

Anterior spinal artery syndrome, also known as anterior cord syndrome or ventral cord syndrome, is a neurologic condition that results in motor paralysis, pain, temperature sensory loss, and occasionally autonomic dysfunction due to occlusion of the anterior spinal artery. This artery supplies the anterior two-thirds of the spinal cord and runs along the entire length of the anterior surface of the spinal cord. Occlusion of the anterior spinal artery leads to reduced blood flow and eventual infarction of the spinal cord, resulting in bilateral lower extremity paresis or paraplegia with loss of pain and temperature sensation. Generally, the patient presentation varies depending on the portion of the spinal cord affected and the time to treatment. In addition to motor deficits and loss of pain and temperature sensation, clinical findings include back pain or autonomic dysfunction, such as hypotension, neurogenic bowel or bladder, and sexual dysfunction. The severity of motor dysfunction can range from paraplegia to quadriplegia, depending on the rostral level of the involved spinal cord. This clinical manifestation is known as anterior spinal artery syndrome. Typically, proprioception, vibratory sense, and fine touch are preserved. The neurological deficits manifest below the level of insult due to the anatomical distribution of the spinal cord tracts. The anterior spinal artery forms from the bilateral vertebral arteries at the foramen magnum and runs as an uninterrupted artery within the anterior median sulcus of the spinal cord to the conus medullaris. Radicular arteries enter the spinal canal through the intervertebral foramen and primarily supply the nerve roots; however, some anastomoses contribute to the anterior spinal artery. The largest of these radicular arteries is the artery of Adamkiewicz, also known as arteria radicularis magna, which most commonly arises from a left intercostal artery between segments T9 to T12 but can vary anatomically. The anterior spinal artery branches into small sulcal and penetrating arteries that enter the body of the spinal cord. The anterior spinal artery supplies blood to the spinal cord's bilateral anterior and lateral horns and the bilateral spinothalamic and corticospinal tracts. The anterior horns and corticospinal tracts control the somatic motor system from the neck to the feet. The lateral horns, spanning levels T1 to L2 of the spinal cord, comprise the neuronal cell bodies of the sympathetic nervous system. The spinothalamic tracts relay pain, temperature, and sensory information. The anterior spinal artery, with a few radicular artery contributions, is the sole source of blood supply to these areas of the spinal cord through sulcal and penetrating arteries. Ischemia of the anterior spinal artery causes symptoms consistent with the dysfunction of these tracts. As the anterior spinal artery is formed from the more cephalad vertebral arteries and runs caudally, the more rostral the location of ischemia, the more widespread or severe the symptoms. As the lateral horns are located between the T1 and L2 of the spinal cord, autonomic symptoms are not always present if ischemia does not involve this region. Proprioception, vibratory sense, two-point discrimination, and fine touch are not affected in anterior cord syndrome and are carried by the dorsal column of the spinal cord, which is perfused by 2 posterior spinal arteries running in the posterior lateral sulci. Anterior spinal artery syndrome is a rare cause of spinal cord acute ischemic myelopathy. However, it is the most common cause of spinal cord infarcts. The syndrome is caused by any etiology that decreases or affects blood flow to the anterior spinal artery, with aortic surgery and atherosclerotic disease being the most common causes. Diagnosis of anterior spinal artery syndrome is based on characteristic clinical features and confirmatory neuroimaging studies. The prognosis is generally poor, as no acute management is available. Management focuses on treating the underlying cause and preventing complications. Current treatment follows the same guidelines for cerebral ischemia, atherosclerotic vascular disease, and acute traumatic spinal cord injury.

摘要

脊髓前动脉综合征,也称为脊髓前索综合征或脊髓腹侧综合征,是一种神经系统疾病,由于脊髓前动脉闭塞导致运动麻痹、疼痛、温度感觉丧失,偶尔还会出现自主神经功能障碍。该动脉供应脊髓前三分之二的区域,并沿脊髓前表面全长走行。脊髓前动脉闭塞导致脊髓血流减少并最终梗死,导致双侧下肢轻瘫或截瘫,同时伴有疼痛和温度感觉丧失。一般来说,患者的表现因脊髓受影响的部位和治疗时间而异。除了运动功能障碍以及疼痛和温度感觉丧失外,临床症状还包括背痛或自主神经功能障碍,如低血压、神经源性肠道或膀胱功能障碍以及性功能障碍。运动功能障碍的严重程度可从截瘫到四肢瘫,这取决于受累脊髓的头端水平。这种临床表现被称为脊髓前动脉综合征。通常,本体感觉、振动觉和精细触觉得以保留。由于脊髓神经束的解剖分布,神经功能缺损在损伤水平以下表现出来。脊髓前动脉由枕骨大孔处的双侧椎动脉形成,并作为一条不间断的动脉在脊髓前正中沟内下行至脊髓圆锥。根动脉通过椎间孔进入椎管,主要供应神经根;然而,一些吻合支对脊髓前动脉有供血作用。其中最大的根动脉是Adamkiewicz动脉,也称为大根动脉,它最常起源于T9至T12节段之间的左侧肋间动脉,但在解剖结构上可能有所不同。脊髓前动脉分支为小的沟动脉和穿通动脉,进入脊髓本体。脊髓前动脉为脊髓的双侧前角和外侧角以及双侧脊髓丘脑束和皮质脊髓束供血。前角和皮质脊髓束控制从颈部到足部的躯体运动系统。外侧角跨越脊髓的T1至L2节段,包含交感神经系统的神经元细胞体。脊髓丘脑束传递疼痛、温度和感觉信息。脊髓前动脉在一些根动脉的供血辅助下,通过沟动脉和穿通动脉成为脊髓这些区域唯一的血液供应来源。脊髓前动脉缺血会导致与这些神经束功能障碍一致的症状。由于脊髓前动脉由更靠近头端的椎动脉形成并向尾端走行,缺血部位越靠近头端,症状就越广泛或严重。由于外侧角位于脊髓的T1和L2之间,如果缺血不涉及该区域,自主神经症状并不总是出现。本体感觉、振动觉、两点辨别觉和精细触觉在前索综合征中不受影响,它们由脊髓后索传导,而后索由在脊髓后外侧沟走行的两条脊髓后动脉供血。脊髓前动脉综合征是脊髓急性缺血性脊髓病的罕见病因。然而,它是脊髓梗死最常见的病因。该综合征由任何减少或影响脊髓前动脉血流的病因引起,其中主动脉手术和动脉粥样硬化疾病是最常见的病因。脊髓前动脉综合征的诊断基于特征性的临床特征和确诊性的神经影像学检查。由于没有有效的急性治疗方法,其预后通常较差。治疗重点在于治疗潜在病因并预防并发症。目前的治疗遵循针对脑缺血、动脉粥样硬化性血管疾病和急性创伤性脊髓损伤的相同指南。

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