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

被引:8
|
作者
Vivas, Andrew C. [2 ]
Shimony, Nir [1 ]
Jackson, Eric M. [3 ]
Xu, Risheng [3 ]
Jallo, George I. [1 ,3 ]
Rodriguez, Luis [1 ]
Tuite, Gerald F. [1 ]
Carey, Carolyn M. [1 ]
机构
[1] Johns Hopkins All Childrens Inst Brain Protect Sc, Dept Neurosurg, St Petersburg, FL USA
[2] Univ S Florida, Dept Neurosurg, Tampa, FL USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21205 USA
关键词
Chiari I malformation; complication; hydrocephalus; posterior fossa decompression; subdural hygromas; FORAMEN MAGNUM DECOMPRESSION; CRANIOCERVICAL DECOMPRESSION; SYRINGOMYELIA; COMPLICATION; POPULATION; DURAPLASTY; FOSSA;
D O I
10.3171/2018.4.PEDS17622
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:426 / 438
页数:13
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