脊髓脊髓空洞合并I型Chiari畸形治疗后脊髓-椎管比例失调:说明性病例。

Arjun Nair, Vivek P Gupta, Devin Kolmetzky, Jennifer M Strahle, David D Limbrick
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摘要

背景:I型Chiari畸形(CM-I)是一种常见的小儿神经外科疾病,常伴有脊髓空洞(SM)和脊柱畸形。这三种情况的关联是公认的,但病理生理学联系他们还没有完全阐明。观察:本病例报告描述了一名13岁男性cm - 1型、大完全性鼻窦和进行性脊柱侧凸的不寻常病程,他在后颅底硬脑膜成形术(PFDD)成功减压4个月后出现血管造影阴性的蛛网膜下腔出血(SAH)。值得注意的是,他的颈椎管直径相对于标准数据增加。在出现SAH后,他接受了一个疗程的腰椎脑脊液引流治疗,减轻了他的症状,他没有再发生任何事件。他对PFDD的反应是脊髓直径急剧减少,与他的椎管扩张形成对比。目前,他已经从SAH中恢复了4年,临床表现良好。经验教训:本报告描述了cm - 1和SM的PFDD后的第一例非动脉瘤性SAH,并探讨了SM与椎管直径之间的可能联系。https://thejns.org/doi/10.3171/CASE24272。
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Spinal cord-spinal canal disproportion following treatment for syringomyelia associated with Chiari malformation type I: illustrative case.

Background: Chiari malformation type I (CM-I) is a common pediatric neurosurgical condition that is often associated with syringomyelia (SM) and spine deformity. The association of these three conditions is well recognized, but the pathophysiology linking them has yet to be fully elucidated.

Observations: This case report describes the unusual course of a 13-year-old male with CM-I, a large holocord syrinx, and progressive scoliosis who developed an angiography-negative subarachnoid hemorrhage (SAH) 4 months after successful posterior fossa decompression with duraplasty (PFDD). Notably, his cervical spinal canal diameter was increased relative to normative data. After presenting with SAH, he was treated with a course of lumbar cerebrospinal fluid drainage, which relieved his symptoms, and he had no further incidents. His syrinx responded to PFDD with a dramatic decrease in spinal cord diameter, in contradistinction to his dilated bony spinal canal. He is presently 4 years out from his SAH and doing well clinically.

Lessons: This report describes the first case of nonaneurysmal SAH following PFDD for CM-I and SM and explores a possible link between SM and bony spinal canal diameter. https://thejns.org/doi/10.3171/CASE24272.

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