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颅底 Gorham 病伴 Chiari I 畸形和脑脊液漏:1 例报告。

Cerebrospinal fluid leakage and Chiari I malformation with Gorham's disease of the skull base: A case report.

机构信息

Department of Neurosurgery, Kobe University Graduate School of Medicine, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe 650-0017, Hyogo, Japan.

Department of Neurosurgery, Kobe University Graduate School of Medicine, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe 650-0017, Hyogo, Japan.

出版信息

Neurol Neurochir Pol. 2017 Sep-Oct;51(5):427-431. doi: 10.1016/j.pjnns.2017.06.007. Epub 2017 Jul 13.

Abstract

BACKGROUND

Gorham's syndrome is a rare bone disorder characterized by massive osteolysis of unknown etiology. There are no reports of comorbidity involving cerebrospinal fluid (CSF) leakage and Chiari I malformation with Gorham's syndrome. Here, we report an unusual case of an acute presyrinx state complicated by bacterial meningitis due to CSF leakage and Chiari I malformation associated with Gorham's disease of the skull base.

CASE PRESENTATION

A 25-year-old woman with Chiari I malformation associated with Gorham's syndrome presented with aggressive paresthesia following bacterial meningitis. Axial magnetic resonance imaging (MRI) and computed tomography (CT) cisternography revealed CSF leakage in the right petrous apex. A presyrinx state was diagnosed based on the clinical symptoms and MRI findings. With resolution of the bacterial meningitis, the spinal edema and tonsillar ectopia also improved. Surgical repair of the CSF leakage was performed by an endoscopic endonasal transsphenoidal approach to prevent recurrence of meningitis. The postoperative course was uneventful.

CONCLUSION

Skull base osteolysis in Gorham's syndrome may induce Chiari I malformation and CSF leakage. We should pay attention to acute progression of clinical symptoms because Gorham's syndrome may predispose to development of Chiari I malformation and may be complicated by CSF leakage.

摘要

背景

Gorham 综合征是一种罕见的骨骼疾病,其特征为病因不明的大量骨质溶解。目前尚无脑脊液(CSF)漏合并 Chiari I 畸形与 Gorham 综合征并存的报道。本文报道了一例基底颅底 Gorham 病合并 Chiari I 畸形和 CSF 漏的不典型病例,患者并发急性脊髓空洞前期状态和细菌性脑膜炎。

病例介绍

一名 25 岁女性,患有 Chiari I 畸形合并 Gorham 综合征,在细菌性脑膜炎后出现侵袭性感觉异常。轴向磁共振成像(MRI)和计算机断层扫描(CT)脑池造影显示右侧岩骨尖 CSF 漏。根据临床症状和 MRI 结果诊断为脊髓空洞前期状态。随着细菌性脑膜炎的治愈,脊髓水肿和扁桃体下疝也得到改善。通过经鼻内镜蝶窦入路进行 CSF 漏的手术修复,以防止脑膜炎复发。术后过程顺利。

结论

Gorham 综合征的颅底骨质溶解可能导致 Chiari I 畸形和 CSF 漏。我们应注意临床症状的急性进展,因为 Gorham 综合征可能易发生 Chiari I 畸形,并可能并发 CSF 漏。

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