Anterior Spinal Artery Syndrome Due to Fibrocartilaginous Embolism-Case Report and Treatment Options.

IF 1.1 4区 医学 Q4 CLINICAL NEUROLOGY Neuropediatrics Pub Date : 2024-06-01 Epub Date: 2023-05-10 DOI:10.1055/a-2090-5865
C Menke, I Wieland, E Bueltmann, S Illsinger, H Hartmann
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Abstract

Acute occlusion of the anterior spinal artery and subsequent spinal ischemic infarction leads to anterior spinal artery syndrome characterized by back pain and bilateral flaccid paresis with loss of protopathic sensibility. As a rare cause fibrocartilaginous embolism has been described and is associated with sports or unusual strain.Following gymnastic exercise the day before symptom-onset, a 11 years old girl presented with neck pain, paresis of arms and legs, and impaired deep tendon reflexes. She was unable to lift her arms, grasp, stand, walk and had urinary incontinence. Magnetic resonance imaging revealed a longitudinal T2 hyperintense signal in the anterior spinal cord from C3 to C6 with accompanying bilateral diffusion restriction involving gray matter bilaterally at the level of C4 and C5 and unilaterally at the level of C3/4. The adjacent annulus fibrosus of the intervertebral disc showed a fissure without disc protrusion. Treatment with prednisolone and enoxaparin was started within 12 hours of symptom-onset and continued over 6 days and 8 weeks, respectively. After 2 months, her motor function gradually improved, spinal imaging showed persistent T2 signal hyperintense defects at the level of C4/5. After 5 months, there was only slight impairment affecting elevation and abduction of the right arm.Following physical exercise, the patient suffered from acute anterior spinal cord ischemia with imaging findings in line with a presumed fibrocartilaginous embolism. Unlike most cases, our patient showed almost complete recovery following treatment with prednisolone and enoxaparin. We speculate that the positive outcome is related to rapid treatment initiation.

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纤维软骨栓塞导致的脊髓前动脉综合征--病例报告和治疗方案。
脊髓前动脉急性闭塞和随后的脊髓缺血性梗死会导致脊髓前动脉综合征,其特征是背痛和双侧弛缓性瘫痪,并伴有原发性感觉丧失。一名 11 岁女孩在发病前一天进行体操锻炼后出现颈部疼痛、手脚麻痹和深腱反射受损。她无法抬起手臂、抓握、站立和行走,并伴有尿失禁。磁共振成像显示,C3至C6脊髓前部出现纵向T2高密度信号,并伴有双侧弥散受限,涉及C4和C5水平的双侧灰质和C3/4水平的单侧灰质。邻近的椎间盘纤维环出现裂隙,但没有椎间盘突出。泼尼松龙和依诺肝素治疗在症状出现后12小时内开始,分别持续了6天和8周。2 个月后,她的运动功能逐渐改善,脊柱造影显示 C4/5 水平持续存在 T2 信号高密度缺损。5 个月后,患者的右臂抬高和外展功能仅有轻微障碍。体育锻炼后,患者出现急性脊髓前部缺血,影像学检查结果与推测的纤维软骨栓塞相符。与大多数病例不同,我们的患者在接受泼尼松龙和依诺肝素治疗后几乎完全康复。我们推测,这一积极的结果与快速开始治疗有关。
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来源期刊
Neuropediatrics
Neuropediatrics 医学-临床神经学
CiteScore
2.80
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: For key insights into today''s practice of pediatric neurology, Neuropediatrics is the worldwide journal of choice. Original articles, case reports and panel discussions are the distinctive features of a journal that always keeps abreast of current developments and trends - the reason it has developed into an internationally recognized forum for specialists throughout the world. Pediatricians, neurologists, neurosurgeons, and neurobiologists will find it essential reading.
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