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分流依赖综合征及脑脊液分流术后继发的获得性Chiari畸形:一项9年的纵向观察

Shunt dependency syndrome and acquired Chiari malformation secondary to cerebrospinal fluid diversion procedures: a 9-year longitudinal observation.

作者信息

Yang Chenlong, Deng Xiaofeng, Yang Jun, Xu Yulun

机构信息

Department of Neurosurgery, China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

出版信息

Childs Nerv Syst. 2019 Apr;35(4):707-711. doi: 10.1007/s00381-018-4014-4. Epub 2019 Jan 4.

DOI:10.1007/s00381-018-4014-4
PMID:30610474
Abstract

BACKGROUND

Shunt dependency syndrome is a rare long-term complication of cystoperitoneal (CP) shunting for intracranial arachnoid cysts, which is characterized by acute intracranial hypertension with normal-sized or small ventricles. Additionally, acquired Chiari type I malformations (ACIM) could be infrequently secondary to extrathecal shunt drainage of cerebrospinal fluid.

CASE REPORT

We described a 12-year-old boy who developed shunt dependency syndrome following a CP shunting for treating a temporal arachnoid cyst. To manage this rare complication, we placed a lumboperitoneal (LP) shunt. During the follow-up period, shunt-induced ACIM and concomitant syringomyelia were noted.

CONCLUSION

Shunt dependency syndrome is a rare complication secondary to CP shunting in the treatment of temporal arachnoid cysts, and LP shunting is an effective option to relieve the intracranial hypertension. However, the clinicians should be alert to the ACIM as a rare late complication of cerebrospinal fluid diversion procedures, and the potential protecting effect of the programmable valve should be emphasized.

摘要

背景

分流依赖综合征是颅内蛛网膜囊肿行囊肿 - 腹腔(CP)分流术罕见的长期并发症,其特征为脑室大小正常或较小情况下出现急性颅内高压。此外,后天性 Chiari I 型畸形(ACIM)可能偶尔继发于脑脊液鞘外分流引流。

病例报告

我们描述了一名 12 岁男孩,其在接受 CP 分流术治疗颞叶蛛网膜囊肿后发生了分流依赖综合征。为处理这一罕见并发症,我们置入了腰 - 腹腔(LP)分流管。在随访期间,发现了分流诱导的 ACIM 和并发的脊髓空洞症。

结论

分流依赖综合征是颞叶蛛网膜囊肿治疗中 CP 分流术继发的罕见并发症,LP 分流术是缓解颅内高压的有效选择。然而,临床医生应警惕 ACIM 作为脑脊液分流术罕见的晚期并发症,并应强调可编程阀门的潜在保护作用。

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Shunt dependency syndrome and acquired Chiari malformation secondary to cerebrospinal fluid diversion procedures: a 9-year longitudinal observation.分流依赖综合征及脑脊液分流术后继发的获得性Chiari畸形:一项9年的纵向观察
Childs Nerv Syst. 2019 Apr;35(4):707-711. doi: 10.1007/s00381-018-4014-4. Epub 2019 Jan 4.
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Temporal sylvian fissure arachnoid cyst in children: treatment outcome following microsurgical cyst fenestration with special emphasis on cyst reduction and subdural collection.儿童颞叶脑裂蛛网膜囊肿:显微囊壁开窗术治疗的结果,特别强调囊肿缩小和硬膜下积液。
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本文引用的文献

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Shunt dependency syndrome after cystoperitoneal shunting of arachnoid cysts.蛛网膜囊肿膀胱腹膜分流术后的分流依赖综合征
Childs Nerv Syst. 2014 Mar;30(3):471-6. doi: 10.1007/s00381-013-2248-8. Epub 2013 Aug 29.
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A late complication of CSF shunting: acquired Chiari I malformation.脑脊液分流术的晚期并发症:获得性小脑扁桃体下疝畸形。
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Chiari I malformation in defined genetic syndromes in children: are there common pathways?
儿童特定遗传综合征中的Chiari I型畸形:是否存在共同途径?
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Acquired Chiari type I malformation managed by supratentorial cranial enlargement.通过幕上颅骨扩大术治疗的获得性 Chiari I 型畸形。
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Neurosurgery. 1996 Dec;39(6):1108-12; discussion 1112-3. doi: 10.1097/00006123-199612000-00007.
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Slit ventricle syndrome after cyst-peritoneal shunting for the treatment of intracranial arachnoid cyst.用于治疗颅内蛛网膜囊肿的囊肿-腹腔分流术后裂隙脑室综合征
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