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终末期脊髓空洞症患者切断终丝后的手术效果。

Surgical outcomes by sectioning a filum terminale in patients with terminal syringomyelia.

作者信息

Ishisaka Eitaro, Usami Kenichi, Ogiwara Hideki

机构信息

Division of Neurosurgery, National Center for Child Health and Development, Okura 2-10-1, Setagaya-ku, Tokyo, 157-8535, Japan.

出版信息

Childs Nerv Syst. 2020 Dec;36(12):3035-3039. doi: 10.1007/s00381-020-04615-5. Epub 2020 Apr 21.

Abstract

BACKGROUND

Although terminal syringomyelia suggests a tethered spinal cord, a consensus has still not been established for surgical indications, when there are no associated abnormalities or only minor associated abnormalities. We analyzed surgical outcomes of sectioning a filum terminale in patients with terminal syringomyelia to elucidate the significance of untethering surgery.

METHODS

Fifty-seven pediatric patients with terminal syringomyelia who underwent untethering via sectioning the filum terminale between 2007 and 2018 were retrospectively analyzed. Postoperative outcomes of symptoms and MRI findings were evaluated.

RESULTS

Of 57 patients, 40 had other associated abnormalities (25 with filar lipoma and 29 with low conus medullaris) that could be responsible for tethered cord. Nineteen patients had symptoms. The mean age at the time of surgery was 18 months (3-96 months). The mean follow-up period was 3.3 years (1-9 years). Preoperative symptoms improved in 9 patients (47%) after surgery. At 1 year after the surgery, the size of syringomyelia decreased in 19 (33%), increased in 4 (8%), and did not change in 34 (69%) patients. Of 28 patients who were followed up for more than 3 years, the size decreased in 17 (61%), increased in 1 (4%), and did not change in 10 (35%).

CONCLUSION

When untethering was performed by sectioning a filum terminale, the size of terminal syringomyelia decreased in more than half of patients in the long term. Sectioning the filum terminale demonstrated the possibility of radiological and clinical improvement in patients with terminal syringomyelia.

摘要

背景

尽管终丝空洞症提示脊髓栓系,但对于无相关异常或仅有轻微相关异常时的手术指征尚未达成共识。我们分析了终丝空洞症患者切断终丝的手术结果,以阐明松解手术的意义。

方法

回顾性分析2007年至2018年间57例因切断终丝行松解术的小儿终丝空洞症患者。评估术后症状及MRI表现的结果。

结果

57例患者中,40例有其他可能导致脊髓栓系的相关异常(25例伴有终丝脂肪瘤,29例伴有低位圆锥)。19例患者有症状。手术时的平均年龄为18个月(3 - 96个月)。平均随访期为3.3年(1 - 9年)。9例(47%)患者术后术前症状改善。术后1年,19例(33%)患者的空洞大小减小,4例(8%)增大,34例(69%)无变化。在28例随访超过3年的患者中,17例(61%)空洞大小减小,1例(4%)增大,10例(35%)无变化。

结论

通过切断终丝进行松解手术时,从长期来看,超过半数患者的终丝空洞症大小减小。切断终丝显示了终丝空洞症患者在影像学和临床方面改善的可能性。

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