巨细胞动脉炎的神经眼科表现综述。

IF 1.6 Q3 OPHTHALMOLOGY
Journal of Ophthalmic & Vision Research Pub Date : 2025-06-24 eCollection Date: 2025-01-01 DOI:10.18502/jovr.v20.15248
Jo-Ann Khoury, Danah Albreiki
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引用次数: 0

摘要

巨细胞动脉炎(GCA)是影响50岁以上成年人的最常见的大、中型血管炎。由于其通过全身性炎症过程引起的急性缺血性损伤,GCA是一种具有永久性视力丧失风险的医疗紧急情况。因此,早期干预至关重要。患者通常有充分的系统性表现,如下颌跛行、头痛、头皮压痛和疲劳。这些患者通常接受血液炎症标志物检查和颞动脉活检。然而,临床表现差异很大,可能被伪装成神经眼科的表现,而不是GCA的病理特征。我们进行了一项回顾,讨论记录的神经眼科表现,并提供罕见的表现,以帮助避免其诊断陷阱。纳入文章的结果分为传入和传出神经-眼科表现。根据我们的文献回顾,记录的主要传入表现为缺血性视神经病变、视网膜动脉闭塞、脉络膜梗死、眼缺血综合征、眶炎综合征和中风引起的视野丧失。传出表现包括颅神经病变(第3、4、6区)、眼外肌缺血、眼核间麻痹。其他罕见的原因包括睫状神经节受累引起的强直性瞳孔、葡萄膜炎和脑病。如果怀疑GCA,除了询问全身症状和做完整的神经眼科检查外,还应送这些患者进行炎症血清学标志物检查和颞动脉活检(TAB)。如果临床怀疑仍然很高,应立即开始使用大剂量类固醇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuro-ophthalmic Manifestations of Giant Cell Arteritis: A Review.

Giant cell arteritis (GCA) is the most common vasculitis of large and medium vessels affecting adults over the age of 50. Due to its acute ischemic damage through a systemic inflammatory process, GCA is a medical emergency with the risk of permanent vision loss. Therefore, early intervention is critical. Patients often present with well-documented systemic manifestations such as jaw claudication, headache, scalp tenderness, and fatigue. These patients are usually subject to blood tests for inflammatory markers and temporal artery biopsy. However, clinical manifestations vary considerably and may masquerade as neuro-ophthalmic manifestations that are not pathognomonic of GCA. We conducted a review to discuss documented neuro-ophthalmic manifestations and provide insight into the rare presentations to help avoid pitfalls in its diagnosis. Findings from the included articles were sorted into afferent and efferent neuro-ophthalmic manifestations. According to our literature review, the main afferent manifestations documented are ischemic optic neuropathy, retinal artery occlusion, choroidal infarction, ocular ischemic syndrome, orbital inflammatory syndrome, and strokes causing visual field loss. The efferent manifestations include cranial neuropathy (3 rd , 4 th , and 6 th ), extraocular muscle ischemia, and internuclear ophthalmoplegia. Other rare causes are tonic pupil from ciliary ganglion involvement, uveitis, and encephalopathy. If GCA is suspected, in addition to inquiring about systemic symptoms and doing a complete neuro-ophthalmic exam, these patients should be sent for inflammatory serological markers, as well as temporal artery biopsy (TAB). If clinical suspicion remains high, high-dose steroids should be started immediately.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
63
审稿时长
30 weeks
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