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[粘连性蛛网膜炎继发脊髓空洞症:临床特征及分流手术疗效]

[Syringomyelia secondary to adhesive arachnoiditis: clinical profiles and efficacy of shunt operations].

作者信息

Kamada K, Iwasaki Y, Hida K, Abe H, Isu T

机构信息

Department of Neurosurgery, Hokkaido University School of Medicine.

出版信息

No Shinkei Geka. 1993 Feb;21(2):135-40.

PMID:8459899
Abstract

The authors report nine cases of syringomyelia secondary to adhesive arachnoiditis treated in our institute from 1982 to 1991. Neurological signs, radiological features, and results of surgical treatment were reviewed. Common initial manifestations in association with syringomyelia were spastic paraparesis in 8 patients (88.9%), regional sensory loss in 4 (44.4%), neurogenic bladder in 4 (44.4%), and somatic pain in 2 (22.2%). All the neurological symptoms or signs progressed gradually for years. All the patients were treated with various modes of shunt operations, including syringo-peritoneal shunt in seven patients, syringo-subarachnoid shunt in one, and ventriculo-peritoneal shunt in one, respectively. Three patients who failed to resolve their major complaints after the first surgery further received syringo-peritoneal shunts. Postsurgical follow-up periods ranged from 18 months to 10 years. Serial MR imaging revealed a significant reduction of the size of syringomyelia in 8 of 9 patients. However only 6 patients showed certain improvement of neurological deficits. Three patients who failed to improve clearly had a long (beyond 15 years) history of syringomyelia before the first surgical treatment. A total of 11 syringo-peritoneal shunts were done in 8 patients of whom 5 patients improved neurologically. It was noticed that 4 of 5 successful syringo-peritoneal shunts were placed in the caudal level of the syrinx. In conclusion, syringo-peritoneal shunt may be at present an optimal mode of surgical management for syringomyelia secondary to adhesive arachnoiditis. In addition, we would like to recommend that follow-up serial MR imaging be done for patients having adhesive arachnoiditis in order to detect syringomyelia as early as possible.

摘要

作者报告了1982年至1991年在我院治疗的9例粘连性蛛网膜炎继发脊髓空洞症病例。回顾了神经体征、放射学特征及手术治疗结果。脊髓空洞症常见的初始表现为8例患者(88.9%)出现痉挛性截瘫,4例(44.4%)出现局部感觉丧失,4例(44.4%)出现神经源性膀胱,2例(22.2%)出现躯体疼痛。所有神经症状或体征均逐年逐渐进展。所有患者均接受了不同方式的分流手术,包括7例行脊髓空洞-腹腔分流术,1例行脊髓空洞-蛛网膜下腔分流术,1例行脑室-腹腔分流术。3例首次手术后主要症状未缓解的患者进一步接受了脊髓空洞-腹腔分流术。术后随访时间为18个月至10年。系列磁共振成像显示,9例患者中有8例脊髓空洞大小显著缩小。然而,只有6例患者的神经功能缺损有一定改善。3例改善不明显的患者在首次手术治疗前有较长(超过15年)的脊髓空洞病史。8例患者共进行了11次脊髓空洞-腹腔分流术,其中5例神经功能改善。值得注意的是,5例成功的脊髓空洞-腹腔分流术中,有4例放置在脊髓空洞的尾端水平。总之,目前脊髓空洞-腹腔分流术可能是粘连性蛛网膜炎继发脊髓空洞症的最佳手术治疗方式。此外,我们建议对患有粘连性蛛网膜炎的患者进行系列磁共振成像随访,以便尽早发现脊髓空洞症。

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