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放置硬膜囊分流管治疗梗阻性原发性脊髓空洞症。

Thecal shunt placement for treatment of obstructive primary syringomyelia.

作者信息

Lam Sandi, Batzdorf Ulrich, Bergsneider Marvin

机构信息

Department of Neurosurgery, University of California Los Angeles, California, USA.

出版信息

J Neurosurg Spine. 2008 Dec;9(6):581-8. doi: 10.3171/SPI.2008.10.08638.

Abstract

OBJECT

The most commonly reported treatment of primary syringomyelia has been laminectomy with duraplasty or direct shunting from the syrinx cavity. Diversion of cerebrospinal fluid (CSF) from the spinal subarachnoid space to peritoneal, atrial, or pleural cavities has been described previously in only a few case reports. Shunting of the CSF from the subarachnoid space rostral to the level of myelographic blockage may reduce the filling force of the syrinx cavity and avoids myelotomy and manipulation of the spinal cord parenchyma. The authors report on 7 patients who underwent thecal shunt placement for primary spinal syringomyelia.

METHODS

This study is a retrospective review of a consecutive series. The authors reviewed the medical records and neuroimaging studies of 7 adult patients with posttraumatic, postsurgical, or postinflammatory syringomyelia treated with thecoperitoneal, thecopleural, or thecoatrial shunt placement at the University of California Los Angeles Medical Center. Myelographic evidence of partial or complete CSF flow obstruction was confirmed in the majority of patients. The mean duration of follow-up was 33 months (range 6-104 months).

RESULTS

Six (86%) of 7 patients showed signs of clinical improvement, whereas 1 remained with stable clinical symptoms. Of the 6 patients with available postoperative imaging, each demonstrated a reduction in syrinx size. Three patients (43%) had > or = 1 complication, including shunt-induced cerebellar tonsillar descent in 1 patient and infections in 2.

CONCLUSIONS

If laminectomy with duraplasty is not possible for the treatment of primary syringomyelia, placement of a thecoperitoneal shunt (or thecal shunt to another extrathecal cavity) should be considered. Although complications occurred in 3 of 7 patients, the complication rate was outweighed by a relatively high symptomatic and imaging improvement rate.

摘要

目的

原发性脊髓空洞症最常报道的治疗方法是椎板切除术加硬脊膜成形术或直接从空洞腔分流。此前仅有少数病例报告描述了将脑脊液(CSF)从脊髓蛛网膜下腔分流至腹膜腔、心房或胸腔。将蛛网膜下腔的脑脊液分流至脊髓造影阻塞平面上方可降低空洞腔的充盈压力,并避免脊髓切开术和对脊髓实质的操作。作者报告了7例因原发性脊髓空洞症接受鞘内分流术的患者。

方法

本研究是对一系列连续病例的回顾性分析。作者回顾了加利福尼亚大学洛杉矶分校医学中心7例因创伤后、手术后或炎症后脊髓空洞症接受腹膜腔、胸腔或心房鞘内分流术的成年患者的病历和神经影像学研究。大多数患者证实有部分或完全脑脊液流动阻塞的脊髓造影证据。平均随访时间为33个月(范围6 - 104个月)。

结果

7例患者中有6例(占86%)显示出临床改善迹象,而1例临床症状保持稳定。在6例有术后影像学资料的患者中,每例均显示空洞大小缩小。3例患者(占43%)出现≥1种并发症,包括1例因分流导致小脑扁桃体下疝和2例感染。

结论

如果无法通过椎板切除术加硬脊膜成形术治疗原发性脊髓空洞症,则应考虑放置腹膜腔分流术(或鞘内分流至另一个鞘外腔)。虽然7例患者中有3例出现并发症,但相对较高的症状改善率和影像学改善率超过了并发症发生率。

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