首页> 美国卫生研究院文献>Neurologia medico-chirurgica >Atypical Cerebellar Slump Syndrome and External Hydrocephalus following Craniocervical Decompression for Chiari I Malformation: Case Report
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Atypical Cerebellar Slump Syndrome and External Hydrocephalus following Craniocervical Decompression for Chiari I Malformation: Case Report

机译:Chiari I畸形经颅颈减压后的非典型性小脑塌陷综合征和外部脑积水

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摘要

Symptomatic cerebellar slump (CS) and external hydrocephalus (EH) are amongst the rarer complications of foramen magnum decompression (FMD) for Chiari I malformation (CM). CS typically presents with delayed onset headache related to dural traction or with neurological deficit offsetting the benefit of FMD. EH, consisting of ventriculomegaly along with subdural fluid collection(s) (SFCs), has been related to cerebrospinal fluid egress from a tiny breach in an otherwise intact arachnoid. We describe the case of a 21-year-old man with CM and syringomyelia who presented with impaired gag, spastic quadriparesis, and raised intracranial pressure 1 week following an uneventful FMD during which the arachnoid had been widely fenestrated. Magnetic resonance imaging (MRI) showed an infratentorial SFC, dilated aqueduct and triventriculomegaly, features of CS, and a residual but resolving syrinx. His symptoms resolved following a high pressure ventriculo-peritoneal shunt. At a 6-month follow-up visit, he was asymptomatic and demonstrated partial resolution of the syrinx, with no recurrence of the SFC. The unusual features in the clinical course of this patient were an atypical CS syndrome presenting with concomitantly resolving syringomyelia, and the development of EH after a wide arachnoidal fenestration. This is the first case in indexed literature describing such a combination of unusual postoperative complications of a FMD. A hypothesis is presented to explain the clinico-radiological findings of the case.
机译:有症状的小脑下陷(CS)和外部脑积水(EH)是Chiari I畸形(CM)引起的大孔减压(FMD)的罕见并发症。 CS通常表现为与硬脑膜牵拉相关的迟发性头痛或神经功能缺损,抵消了FMD的益处。 EH由脑室肥大和硬脑膜下积液(SFC)组成,与脑脊液从原本完整的蛛网膜的微小裂口流出有关。我们描述了一个21岁的CM和脊髓空洞症的男性患者的情况,该患者在正常FMD(蛛网膜已广泛开窗)后1周出现堵嘴,痉挛性四肢瘫痪和颅内压升高。磁共振成像(MRI)显示了下颌SFC,扩张的输水管和三脑巨肿,CS的特征以及残留但可分辨的syrinx。高压心室-腹膜分流后症状消失。在为期6个月的随访中,他没有症状,并显示出syrinx的部分消退,SFC没有复发。该患者在临床过程中的不寻常特征是伴有解决性脊髓空洞症的非典型性CS综合征和广泛蛛网膜开窗后EH的发展。这是索引文献中描述FMD异常术后并发症的这种组合的第一例。提出了一个假设来解释该病例的临床放射学发现。

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