Suppr超能文献

翼点开颅切除额部脑膜瘤后出现眶隔综合征但无眶内肿块或眼球受压的证据:病例报告及文献复习。

Orbital Compartment Syndrome without Evidence of Orbital Mass or Ocular Compression After Pterional Craniotomy for Removal of Meningioma of the Frontal Lobe: A Case Report and Literature Review.

机构信息

Department of Anesthesiology, Uniformed University of the Health Sciences, Bethesda, Maryland, USA; American Board of Psychiatry and Neurology, North Deerfield, Illinois, USA; American Board of Anesthesiology, Raleigh, North Carolina, USA.

Division of Neurosurgery, Department of Surgery, Uniformed University of the Health Sciences, Bethesda, Maryland, USA.

出版信息

World Neurosurg. 2020 Jul;139:588-591. doi: 10.1016/j.wneu.2020.04.094. Epub 2020 Apr 25.

Abstract

BACKGROUND

Orbital compartment syndrome (OCS) is a rare post operative complication of Neurosurgery. It presents typically acutely with loss of vision, loss of pupillary reaction, and limitation of extraocular movement. The etiology of OCS is most typically associated with increased pressure from a mass lesion in the orbit compromising the blood supply of orbital structures. Emergent bedside decompression of the orbit by lateral canthotomy is indicated to quickly treat OCS in an attempt to save visual acuity and extraocular function.

CASE DESCRIPTION

We report a 76-year-old male patient whose magnetic resonance imaging of the brain demonstrated an anterior right frontal broad dural-based homogenously enhancing mass measuring 6.0 × 3.1 × 6.3 cm after he presented with 1-year of progressive cognitive dysfunction. A right-sided pterional craniotomy and resection of mass was performed under general anesthesia, with an uncomplicated intraoperative course. Postoperatively, the right eye was noted to have an afferent pupillary defect, complete ophthalmoplegia, ptosis, and significant resistance to retropulsion. Emergent ophthalmologic consultation confirmed the ocular examination, and the diagnosis of right OCS was suspected. A right lateral canthotomy and cantholysis was performed by the ophthalmologist at the bedside. The fundoscopic retinal evaluation was normal. Noncontrast computed tomography of the head demonstrated expected postoperative changes and mild edema of the right frontal lobe without evidence of acute hemorrhage. There was no retro-orbital hematoma, but the right extra-ocular muscles appeared edematous compared to the left. No light perception and ophthalmoplegia continued in the right eye.

CONCLUSIONS

This case demonstrates that although very rare, OCS can occur without compression of the eye or an intra-orbital mass. Visual loss is a devastating complication. Constant vigilance to ensure adequate arterial and venous supply to the orbit, with great care to prevent external compression on the eye, hopefully, will continue to make this complication rare.

摘要

背景

眼眶间隔综合征(OCS)是神经外科术后罕见的并发症。它通常表现为视力丧失、瞳孔反应丧失和眼球运动受限。OCS 的病因最常与眼眶内肿块引起的压力增加有关,从而影响眼眶结构的血液供应。床边紧急行眼眶外侧切开减压术,以快速治疗 OCS,试图挽救视力和眼球运动功能。

病例描述

我们报告了一例 76 岁男性患者,其脑部磁共振成像显示右侧额前部有一个 6.0×3.1×6.3cm 的宽基硬脑膜增强肿块,患者在出现进行性认知功能障碍 1 年后就诊。患者在全身麻醉下行右侧翼点开颅术和肿块切除术,术中过程顺利。术后发现右眼有传入性瞳孔缺损、完全眼肌瘫痪、上睑下垂和明显的眼球后退抵抗。紧急眼科会诊确认了眼部检查结果,并怀疑为右侧 OCS。眼科医生在床边行右眼外侧切开和切开松解术。眼底视网膜评估正常。头部非增强 CT 显示术后预期改变和右侧额叶轻度水肿,无急性出血证据。无眶后血肿,但与左侧相比,右侧眼外肌显得水肿。右眼无光感和眼肌瘫痪持续存在。

结论

本病例表明,尽管非常罕见,但 OCS 可在不压迫眼球或眼眶内肿块的情况下发生。视力丧失是一种毁灭性的并发症。始终保持警惕,确保眼眶有足够的动脉和静脉供应,并特别注意防止眼球受到外部压迫,有望使这种并发症继续保持罕见。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验