Department of Radiology, Duke University Medical Center, Durham, North Carolina, USA.
J Neurosurg. 2011 Sep;115(3):641-4. doi: 10.3171/2011.3.JNS102164. Epub 2011 Apr 29.
In the scientific literature, syringohydromyelia has only rarely been reported in association with spontaneous intracranial hypotension. Management of the syringohydromyelia in these patients has heretofore involved relatively invasive surgical procedures. The authors report the first case of syringohydromyelia in the setting of intracranial hypotension successfully treated with CT-guided epidural blood patches. This case is important in that it represents a potential minimally invasive treatment strategy. Furthermore, the case also highlights the need to consider spontaneous intracranial hypotension when clinically appropriate as a cause of syrinx in patients with cerebellar tonsillar ectopia, in whom the lesion might otherwise be misclassified as a Chiari I malformation. Finally, the responses to the various attempted treatments offer insight into the pathophysiology of this syringohydromyelia, which may differ from classical models of syrinx formation.
在科学文献中,与自发性颅内低血压相关的 脑积液压迫脊髓空洞症极为罕见。此类患者的脊髓空洞症治疗方法以往涉及相对有创的手术。作者报告首例自发性颅内低血压合并脑积液压迫脊髓空洞症病例,采用 CT 引导下硬膜外血贴治疗成功。该病例具有重要意义,代表了一种潜在的微创治疗策略。此外,该病例还强调了在临床适当的情况下,应将自发性颅内低血压作为小脑扁桃体下疝患者脊髓空洞症的病因加以考虑,否则,此类病变可能会被误诊为 Chiari I 畸形。最后,各种尝试性治疗的反应为这种脑积液压迫脊髓空洞症的病理生理学提供了深入了解,这可能与经典的脊髓空洞症形成模式不同。