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寰枕减压术后伴 Chiari I 畸形的脊髓空洞症治疗失败:我们应该如何处理?

Treatment failure of syringomyelia associated with Chiari I malformation following foramen magnum decompression: how should we proceed?

机构信息

Departments of Neurosurgery and Pediatric Neurosurgery, Tel-Aviv Medical Center and Dana Children's Hospital Tel Aviv, Tel Aviv University, 6 Weizmann Street, Tel Aviv, Israel.

Department of Neurosurgery and Division of Pediatric Neurosurgery, University Hospital of Basel, Basel, Switzerland.

出版信息

Neurosurg Rev. 2019 Sep;42(3):705-714. doi: 10.1007/s10143-018-01066-0. Epub 2018 Dec 15.

Abstract

The preferred treatment of patients with persistent, recurrent, or progressive syringomyelia after foramen magnum decompression (FMD) for Chiari I (CMI)-associated syringomyelia is controversial, and may include redo FMD, stabilization, or shunting procedures (such as syringopleural or syringo-subarachnoid shunts). We describe our experience in treating these patients and discuss the treatment modalities for these patients. We retrospectively collected data of CMI patients with persistent, recurrent, or progressive syringomyelia after FMD. In addition to baseline characteristics, surgical treatments and neurological and radiological outcomes were assessed. Further, we assessed through uni- and multivariate analyses possible technical, surgical, and radiological factors which might lead to failed FMD. Between 1998 and 2017, 48 consecutive patients (35 females (73%), average age 16.8 ± 11.5 years) underwent FMD for a syringomyelia-Chiari complex. Twenty-four patients (50%) underwent surgical treatment for a persistent (n = 10), progressive (n = 12), or recurrent (n = 2) syringomyelia 21.4 ± 27.9 months (median 14.6 months, range 12 days-134.9 months) after FMD. Of all analyzed factors, only extradural FMD was significantly associated with lower failure rates. Two patients (8%) underwent redo FMD, 18 (75%) underwent 19 syringo-subarachnoid-shunts, and 4 (17%) had 6 cranial CSF diversion procedures. The overall follow-up time was 40.1 ± 47.4 months (median 25 months, range 3-230 months). Based on our results, 50% of the patients undergoing FMD for syringomyelia-Chiari complex may require further surgical treatment due to persistent, progressive, or recurrent syringomyelia. Treatment should be tailored to the suspected underlying pathology. A subgroup of patients may be managed conservatively; however, these patients need close clinical and radiological follow-ups. The technical aspects of FMD in CMI-syrinx complex should be the focus of larger studies, as an effort to improve failure rates.

摘要

寰枕减压术(FMD)治疗 Chiari I 畸形(CMI)相关脊髓空洞症后持续性、复发性或进行性脊髓空洞症患者的首选治疗方法存在争议,可能包括再次 FMD、稳定或分流手术(如脊髓空洞-胸腔或脊髓空洞-蛛网膜下腔分流)。我们描述了我们治疗这些患者的经验,并讨论了这些患者的治疗方法。我们回顾性收集了 FMD 治疗后持续性、复发性或进行性脊髓空洞症的 CMI 患者的数据。除了基线特征外,还评估了手术治疗和神经学及影像学结果。此外,我们通过单因素和多因素分析评估了可能导致 FMD 失败的技术、手术和影像学因素。1998 年至 2017 年间,48 例连续患者(35 例女性(73%),平均年龄 16.8±11.5 岁)因脊髓空洞-小脑扁桃体复合体行 FMD。24 例患者(50%)因持续性(n=10)、进行性(n=12)或复发性(n=2)脊髓空洞症,在 FMD 后 21.4±27.9 个月(中位数 14.6 个月,范围 12 天-134.9 个月)行手术治疗。在所有分析的因素中,只有硬膜外 FMD 与较低的失败率显著相关。2 例患者(8%)行再次 FMD,18 例(75%)行 19 例脊髓空洞-蛛网膜下腔分流术,4 例(17%)行 6 例颅脊液引流术。总的随访时间为 40.1±47.4 个月(中位数 25 个月,范围 3-230 个月)。根据我们的结果,50%的 FMD 治疗脊髓空洞-小脑扁桃体复合体的患者可能需要进一步的手术治疗,因为存在持续性、进行性或复发性脊髓空洞症。治疗应根据疑似潜在的病理情况进行调整。一部分患者可能需要保守治疗,但这些患者需要密切的临床和影像学随访。CMI 伴脊髓空洞症患者的 FMD 技术方面应作为更大规模研究的重点,以提高手术成功率。

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