Salman Abdul-Rahman, Hur Minjun, Warrington Kenneth J, Garrity James A, Koster Matthew J, Chodnicki Kevin D, Tajfirouz Deena A, Chen John J
George Washington University School of Medicine and Health Sciences (A-RS), Washington, District of Columbia; Department of Ophthalmology (MH, JAG, KDC, DAT, JJC), Mayo Clinic, Rochester, Minnesota; Division of Rheumatology (KJW, MJK), Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota; , Division of Vascular (KJW), Department of Cardiovascular Medicine, Gonda Vascular Center, Mayo Clinic, Rochester, Minnesota; Lake Region Medical Group (JAG), Fergus Falls, Minnesota; and Department of Neurology (DAT, JJC), Mayo Clinic, Rochester, Minnesota.
J Neuroophthalmol. 2024 Sep 4. doi: 10.1097/WNO.0000000000002249.
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.
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.
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.
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.
肉芽肿性多血管炎(GPA),既往称为韦格纳肉芽肿病,是一种罕见的自身免疫性疾病,其特征为中小血管炎症(血管炎)。我们阐述了GPA相关性视神经病变的3种病因(压迫性、炎性或缺血性),并分析了每组患者的初始和最终视力,这可能有助于根据视神经病变的病因预测视力预后。
这是一项对在明尼苏达州罗切斯特市梅奥诊所眼科就诊的诊断为GPA相关性视神经病变患者的回顾性病历审查。仅纳入符合2022年美国风湿病学会/欧洲抗风湿病联盟GPA分类标准的患者。
共确定了12例GPA相关性视神经病变患者。视神经病变的病因中,6例为压迫性,4例为炎性,3例为缺血性。1例患者最初为压迫性视神经病变,数年后出现GPA相关视神经炎。压迫性视神经病变组中有4例患者有眼眶肿物,需要行眼眶切开术以减轻肿物,其余2例患者因硬脑膜炎受压。视神经病变发作时平均最小分辨角对数(logMAR)视力分别为1.50、1.50和0.67(分别相当于Snellen视力20/600、20/600和20/100)。在最后一次随访时,每组患者的平均logMAR视力分别为0.91、1.73和1.10(分别相当于Snellen视力20/160、20/1000和20/250)。
视力预后各不相同,压迫性和炎性视神经病变总共4只眼视力改善,3只眼视力恶化。GPA所致缺血性视神经病变患者在疾病过程中要么视力稳定,要么视力恶化。