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特发性和难治性脊髓空洞症的管理。

The Management of Idiopathic and Refractory Syringomyelia.

机构信息

Department of Paediatric Neurosurgery, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.

Department of Clinical Neurosciences, Edinburgh BioQuarter, Royal Infirmary Edinburgh, Edinburgh, UK.

出版信息

Adv Tech Stand Neurosurg. 2022;45:317-338. doi: 10.1007/978-3-030-99166-1_10.

Abstract

Idiopathic syringomyelia (IS) and refractory syringomyelia (RS) are types of syringomyelia that often pose a management challenge and are associated with long-term clinical sequela. They are usually an epiphenomenon reflecting an underlying pathology where the treatment of the primary cause should be the aim for any surgical intervention. In the case of IS, the initial step is agreeing on the definition of the terms idiopathic and syringomyelia. After a rigorous exhaustive clinic-radiological workup, only IS patients with progressive neurology are treated, usually unblocking subarachnoid cerebrospinal fluid (CSF) pathway obstruction somewhere in the thoracic spinal canal and reserving shunting techniques to nonresponsive cases. Similar to IS, also RS is multifactorial, and its management varies based on the initial pathology, strongly supported by radiological and clinical features. We aim to address this topic focusing on the etiopathology, investigation paradigm, and surgical pathway, formulating algorithms of management with available evidence in literature. Surgical techniques are discussed in detail.

摘要

特发性脊髓空洞症(IS)和难治性脊髓空洞症(RS)是脊髓空洞症的两种类型,常给管理带来挑战,并与长期的临床后遗症有关。它们通常是反映潜在病理的一种表现,因此治疗原发性疾病应是任何手术干预的目标。对于 IS,第一步是就特发性和脊髓空洞症的定义达成一致。在经过严格全面的临床-影像学检查后,只有进展性神经功能障碍的 IS 患者才会接受治疗,通常是在胸段脊髓的某个部位解除蛛网膜下腔脑脊液(CSF)通路阻塞,并将分流技术保留给无反应的病例。与 IS 类似,RS 也是多因素的,其管理根据初始病理而有所不同,强烈支持基于影像学和临床特征的治疗方法。我们旨在通过探讨病因病理、调查模式和手术途径,根据文献中的现有证据制定管理算法,来解决这个问题。手术技术将详细讨论。

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