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正常压力脑积水分流术后迟发性脑室内积气

Delayed Intraventricular Pneumocephalus Following Shunting for Normal-Pressure Hydrocephalus.

作者信息

Verhaeghe Alexander, De Muynck Stijn, Casselman Jan W, Vantomme Nikolaas

机构信息

Department of Neurosurgery, Sint-Jan Hospital Brugge, University Hospitals Leuven, Brugge, Belgium.

Department of Neurosurgery, Sint-Jan Hospital Brugge, University Hospitals Leuven, Brugge, Belgium.

出版信息

World Neurosurg. 2018 Aug;116:174-177. doi: 10.1016/j.wneu.2018.05.112. Epub 2018 May 24.

DOI:10.1016/j.wneu.2018.05.112
PMID:29803572
Abstract

BACKGROUND

Pneumocephalus is usually seen in trauma or cranial surgery. It is rarely reported as a delayed complication of ventriculoperitoneal shunt placement for hydrocephalus secondary to trauma, tumor, or aqueduct stenosis. We describe a case of intraventricular pneumocephalus manifesting 10 months after placement of a shunt for normal-pressure hydrocephalus.

CASE DESCRIPTION

A pressure-regulated ventriculoperitoneal shunt was implanted in an 81-year-old patient after diagnosis of normal-pressure hydrocephalus. He showed postoperative clinical improvement. Routine computed tomography performed 2 months after the procedure showed no abnormalities. He presented 10 months after shunting with a subacute deterioration of gait. Imaging revealed major intraventricular pneumocephalus and a left-sided temporal porencephalic cyst with a small, bony defect in the left petrous bone. A middle fossa approach was performed, and the temporal defect was covered with fascia of the temporal muscle. This resulted in a gradual resolution of pneumocephalus.

CONCLUSIONS

Pneumocephalus after shunting for NPH is rare and described as a complication only during the first 2 postoperative months. This case is unique, as the pneumocephalus developed 10 months after shunting. The combination of an occult, possibly congenital, skull base defect and the insertion of a shunt resulted in delayed intraventricular and intraparenchymal pneumocephalus.

摘要

背景

气颅通常见于外伤或开颅手术。作为创伤、肿瘤或导水管狭窄继发脑积水的脑室腹腔分流术的延迟并发症则鲜有报道。我们描述了一例在常压性脑积水分流术后10个月出现的脑室内气颅病例。

病例描述

一名81岁患者在被诊断为常压性脑积水后植入了压力调节型脑室腹腔分流管。术后他的临床症状有所改善。术后2个月进行的常规计算机断层扫描未显示异常。分流术后10个月,他出现步态亚急性恶化。影像学检查发现主要为脑室内气颅以及左侧颞叶孔洞性脑囊肿,左侧岩骨有一个小的骨质缺损。采用中颅窝入路,用颞肌筋膜覆盖颞部缺损。这使得气颅逐渐消退。

结论

常压性脑积水分流术后气颅罕见,且仅在术后头2个月被描述为一种并发症。该病例独特之处在于气颅在分流术后10个月出现。隐匿的、可能为先天性的颅底缺损与分流管的植入共同导致了延迟性脑室内和脑实质内气颅。

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