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小儿I型Chiari畸形减压术后脑积水和硬膜下积液的管理:病例系列及文献综述

Management of hydrocephalus and subdural hygromas in pediatric patients after decompression of Chiari malformation type I: case series and review of the literature.

作者信息

Vivas Andrew C, Shimony Nir, Jackson Eric M, Xu Risheng, Jallo George I, Rodriguez Luis, Tuite Gerald F, Carey Carolyn M

机构信息

2Department of Neurosurgery, University of South Florida, Tampa, Florida; and.

1Department of Neurosurgery, Johns Hopkins All Children's Institute for Brain Protection Sciences, St. Petersburg.

出版信息

J Neurosurg Pediatr. 2018 Oct;22(4):426-438. doi: 10.3171/2018.4.PEDS17622. Epub 2018 Jul 20.

Abstract

OBJECTIVE

Hydrocephalus associated with subdural hygromas is a rare complication after decompression of Chiari malformation type I (CM-I). There is no consensus for management of this complication. The authors present a series of 5 pediatric patients who underwent CM-I decompression with placement of a dural graft complicated by posterior fossa hygromas and hydrocephalus that were successfully managed nonoperatively.

METHODS

A retrospective review over the last 5 years of patients who presented with hydrocephalus and subdural hygromas following foramen magnum decompression with placement of a dural graft for CM-I was conducted at 2 pediatric institutions. Their preoperative presentation, perioperative hospital course, and postoperative re-presentation are discussed with attention to their treatment regimen and ultimate outcome. In addition to reporting these cases, the authors discuss all similar cases found in their literature review.

RESULTS

Over the last 5 years, the authors have encountered 194 pediatric cases of CM-I decompression with duraplasty equally distributed at the 2 institutions. Of those cases, 5 pediatric patients with a delayed postoperative complication involving hydrocephalus and subdural hygromas were identified. The 5 patients were managed nonoperatively with acetazolamide and high-dose dexamethasone; dosages of both drugs were adjusted to the age and weight of each patient. All patients were symptom free at follow-up and exhibited resolution of their pathology on imaging. Thirteen similar pediatric cases and 17 adult cases were identified in the literature review. Most reported cases were treated with CSF diversion or reoperation. There were a total of 4 cases previously reported with successful nonoperative management. Of these cases, only 1 case was reported in the pediatric population.

CONCLUSIONS

De novo hydrocephalus, in association with subdural hygromas following CM-I decompression, is rare. This presentation suggests that these complications after posterior fossa decompression with duraplasty can be treated with nonoperative medical management, therefore obviating the need for CSF diversion or reoperation.

摘要

目的

与硬膜下积液相关的脑积水是I型Chiari畸形(CM-I)减压术后一种罕见的并发症。对于该并发症的处理尚无共识。作者报告了一系列5例儿科患者,他们接受了CM-I减压并植入硬脑膜移植物,术后并发后颅窝积液和脑积水,均成功接受了非手术治疗。

方法

在2家儿科机构对过去5年中因CM-I行枕骨大孔减压并植入硬脑膜移植物后出现脑积水和硬膜下积液的患者进行回顾性研究。讨论了他们的术前表现、围手术期住院过程及术后再次就诊情况,并关注其治疗方案和最终结局。除了报告这些病例外,作者还讨论了文献回顾中发现的所有类似病例。

结果

在过去5年中,作者在2家机构共遇到194例接受硬脑膜成形术的CM-I儿科减压病例,分布均匀。在这些病例中,识别出5例术后出现脑积水和硬膜下积液延迟并发症的儿科患者。这5例患者接受了乙酰唑胺和高剂量地塞米松的非手术治疗;两种药物的剂量均根据每位患者的年龄和体重进行调整。所有患者在随访时均无症状,影像学检查显示病变消退。文献回顾中识别出13例类似儿科病例和17例成人病例。大多数报告的病例接受了脑脊液分流或再次手术治疗。此前共有4例报告非手术治疗成功。在这些病例中,儿科患者仅报告了1例。

结论

CM-I减压术后新发脑积水合并硬膜下积液很罕见。这表明后颅窝减压并硬脑膜成形术后的这些并发症可通过非手术药物治疗,从而无需脑脊液分流或再次手术。

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