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双侧前引流型硬脑膜动静脉瘘导致双侧后部缺血性视神经病变:一例报告

Bilateral Posterior Ischemic Optic Neuropathy Due to Bilateral Anterior-Drainage Dural Carotid-Cavernous Fistulas: A Case Report.

作者信息

Thammakumpee Kanyarat, Padungkiatsagul Tanyatuth, Putthirangsiwong Bunyada, Chokthaweesak Weerawan, Jindahra Panitha, Kobkitsuksakul Chai, Vanikieti Kavin

机构信息

Department of Ophthalmology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

出版信息

Int Med Case Rep J. 2023 Jan 24;16:53-57. doi: 10.2147/IMCRJ.S401291. eCollection 2023.

Abstract

PURPOSE

To report a case of bilateral posterior ischemic optic neuropathy (PION) due to bilateral anterior-drainage dural carotid-cavernous fistulas (CCFs).

CASE DESCRIPTION

We report on a 62-year-old woman with a history of poorly controlled hypertension who presented with sudden bilateral visual loss and headache for 5 days. She denied a history of head trauma. On examination, her visual acuities were no light perception (NLP) with fixed pupils in both eyes. The ocular motility of both eyes was limited in all directions. Both eyelids were difficult to open. Anterior segment examination revealed bilateral chemosis and episcleral corkscrew vessels. Intraocular pressures were 45 and 48 mmHg in her right and left eyes, respectively. Gonioscopy revealed blood in Schlemm's canal at the nasal angle of the right eye. Fundus examination showed slightly dilated and tortuous retinal veins with normal-appearing optic discs in both eyes. The cup-to-disc ratios were 0.3 bilaterally. Other neurological examinations were unremarkable. Magnetic resonance imaging demonstrated dilation of the bilateral superior ophthalmic veins (SOVs), and marked orbital and periorbital congestion bilaterally. However, there was no compression or stretching of the bilateral optic nerves. Diffusion restriction on diffusion-weighted imaging, with corresponding reduced apparent diffusion coefficient, in the entire bilateral orbital segment of the optic nerves was revealed, consistent with bilateral PION. Magnetic resonance angiography revealed arterialization of the bilateral cavernous sinuses and SOVs. Cerebral angiography confirmed the diagnosis of bilateral anterior-drainage dural CCFs. Treatment with transvenous coil embolization was successful. Three months after embolization, ophthalmic examination demonstrated progressive improvement of aforementioned ophthalmic signs; however, her visual acuities remained NLP in both eyes.

CONCLUSION

To our knowledge, this is the first reported case of bilateral PION due to bilateral anterior-drainage dural CCFs. In spite of its rarity, PION should be considered as a severe, irreversible ophthalmic complication of anterior-drainage dural CCF.

摘要

目的

报告一例因双侧前引流型硬脑膜颈动脉海绵窦瘘(CCF)导致的双侧后部缺血性视神经病变(PION)。

病例描述

我们报告一名62岁女性,有高血压控制不佳病史,突发双侧视力丧失和头痛5天。她否认有头部外伤史。检查时,她的双眼视力均无光感(NLP),瞳孔固定。双眼眼球运动各方向均受限。双眼睑难以睁开。眼前节检查发现双侧球结膜水肿和巩膜表面螺旋状血管。右眼和左眼眼压分别为45和48 mmHg。前房角镜检查显示右眼鼻侧房角小梁网Schlemm管内有血液。眼底检查显示双眼视网膜静脉轻度扩张迂曲,视盘外观正常。双眼杯盘比均为0.3。其他神经系统检查无异常。磁共振成像显示双侧眼上静脉(SOV)扩张,双侧眼眶及眶周明显充血。然而,双侧视神经无受压或牵拉。弥散加权成像显示双侧视神经整个眶内段弥散受限,相应表观弥散系数降低,符合双侧PION。磁共振血管造影显示双侧海绵窦和SOV动脉化。脑血管造影确诊为双侧前引流型硬脑膜CCF。经静脉弹簧圈栓塞治疗成功。栓塞后3个月,眼科检查显示上述眼科体征逐渐改善;然而,她的双眼视力仍为NLP。

结论

据我们所知,这是首例因双侧前引流型硬脑膜CCF导致的双侧PION报告。尽管罕见,但PION应被视为前引流型硬脑膜CCF的一种严重、不可逆的眼科并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/573b/9884056/7043a0f3e6ec/IMCRJ-16-53-g0001.jpg

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