肉芽肿性多血管炎相关性视神经病变的病因和结果:病例系列和文献综述。

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Abdul-Rahman Salman, Minjun Hur, Kenneth J Warrington, James A Garrity, Matthew J Koster, Kevin D Chodnicki, Deena A Tajfirouz, John J Chen
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引用次数: 0

摘要

背景:肉芽肿伴多血管炎(GPA),以前称为韦格纳肉芽肿病,是一种罕见的自身免疫性疾病,以中小型血管的炎症(血管炎)为特征。我们描述了 GPA 相关性视神经病变的 3 种病因(压迫性、炎症性或缺血性),并分析了每组患者的初始和最终视力(VAs),这可能有助于根据视神经病变的病因预测视力预后:这是对明尼苏达州罗切斯特梅奥诊所眼科确诊为 GPA 相关性视神经病变患者的回顾性病历审查。只有符合2022年美国风湿病学会/欧洲风湿病学协会联盟GPA分类标准的患者才被纳入:结果:共发现12名GPA相关性视神经病变患者。6名患者的视神经病变病因为压迫性,4名患者为炎症性,3名患者为缺血性。一名患者最初为压迫性视神经病变,多年后出现了与 GPA 相关的视神经炎。压迫性视神经病变组中有 4 名患者有眼眶肿块,需要进行眼眶切开术进行剥离,其余 2 名患者的压迫性视神经病变是由帕奇脑膜炎引起的。视神经病变发病时的平均最小分辨角对数(logMAR)VA分别为1.50、1.50和0.67(斯奈伦等效视力分别为20/600、20/600和20/100)。最后一次随访时,各组的平均对数视力分别为0.91、1.73和1.10(斯奈伦视力等效值分别为20/160、20/1000和20/250):视力结果各不相同,压迫性和炎症性视神经病变共有4只眼睛的视力有所改善,3只眼睛的视力恶化。GPA引起的缺血性视神经病变患者在病程中要么病情稳定,要么恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Etiologies and Outcomes of Granulomatosis With Polyangiitis-Associated Optic Neuropathy: A Case Series and Review of the Literature.

Background: Granulomatosis with polyangiitis (GPA), formerly known as Wegener granulomatosis, is a rare autoimmune disease characterized by inflammation of small- to medium-sized blood vessels (vasculitis). We described the 3 causes of GPA-associated optic neuropathy (compressive, inflammatory, or ischemic) and analyzed initial and final visual acuities (VAs) in each group, which could potentially help prognosticate visual outcomes depending on the etiology of optic neuropathy.

Methods: This was a retrospective chart review of patients who were diagnosed with GPA-associated optic neuropathy and were seen in the Department of Ophthalmology at Mayo Clinic in Rochester, Minnesota. Only patients who met the 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology GPA classification criteria were included.

Results: A total of 12 patients with GPA-associated optic neuropathy were identified. The etiology of the optic neuropathy was compressive in 6 patients, inflammatory in 4 patients, and ischemic in 3 patients. One patient had compressive optic neuropathy initially, then presented with GPA-related optic neuritis years later. Four patients in the compressive optic neuropathy group had orbital masses requiring orbitotomy for debulking, and the remaining 2 patients had compression from pachymeningitis. Average logarithm of the minimum angle of resolution (logMAR) VA at optic neuropathy onset was 1.50, 1.50, and 0.67 (Snellen equivalent 20/600, 20/600, and 20/100, respectively). At the last follow-up, average logMAR VA was 0.91, 1.73, and 1.10 (Snellen equivalent 20/160, 20/1,000, and 20/250, respectively) for each group.

Conclusion: Visual outcomes were variable, with compressive and inflammatory optic neuropathies showing improvement in 4 eyes and worsening in 3 eyes in total. Patients with ischemic optic neuropathy from GPA were either stable or worsened over the course of the disease.

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来源期刊
Journal of Neuro-Ophthalmology
Journal of Neuro-Ophthalmology 医学-临床神经学
CiteScore
2.80
自引率
13.80%
发文量
593
审稿时长
6-12 weeks
期刊介绍: The Journal of Neuro-Ophthalmology (JNO) is the official journal of the North American Neuro-Ophthalmology Society (NANOS). It is a quarterly, peer-reviewed journal that publishes original and commissioned articles related to neuro-ophthalmology.
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