Ocular and orbital manifestations of granulomatosis with polyangiitis: a systematic review of published cases.

Kayvon Ahmad Moin, Madeleine Marta Yeakle, Allison Margaret Parrill, Victoria Anne Garofalo, Allen Raphael Tsiyer, Daniel Bishev, Dhir Gala, Joshua Fogel, Alexander James Hatsis, Tyler Daniel Wickas, Prachi Anand, Marcelle Morcos
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Abstract

Objective: Granulomatosis with polyangiitis (GPA) is an autoimmune disorder characterized by necrotizing granulomatous inflammation of small and medium-sized vessels. This systematic review aimed to highlight the most common ophthalmic manifestations and to uncover their associations with antineutrophil cytoplasmic antibody (ANCA) positivity and the presence of granulomas. Methods: A literature search of PubMed, Web of Science, and Scopus electronic databases was performed from journal inception to March 21, 2021, for case reports and a series of ophthalmic GPAs. Cytoplasmic-ANCA (c-ANCA), perinuclear-ANCA (p-ANCA), and granulomas were analyzed against many ophthalmic signs and symptoms. 306 patients with GPA were retrospectively studied. Results: Granulomas were present in 47.7% of our sample, c-ANCA in 59.2%, and p-ANCA in 10.8%. Scleritis was significantly associated with higher odds for c-ANCA positivity. Eye discharge, episcleritis, proptosis, and central nervous system (CNS) involvement were each significantly associated with lower odds for c-ANCA positivity. Orbital mass was significantly associated with lower odds for p-ANCA positivity. CNS involvement was significantly associated with higher odds for p-ANCA positivity (OR:3.08, 95% CI:1.02, 9.36, p=0.047) and orbital mass was significantly associated with lower odds for p-ANCA positivity. Conclusions: We recommend that clinicians should consider ocular or orbital GPA in patients presenting with non-specific eye complaints, such as vision impairment, orbital mass, or proptosis, and obtain further assessments to determine the possible presence of granuloma, c-ANCA, or p-ANCA. Abbreviations: GPA = Granulomatosis with Polyangiitis, ANCA = antineutrophil cytoplasmic antibody, c-ANCA = cytoplasmic-ANCA, p-ANCA = perinuclear-ANCA, CNS = central nervous system, AAVs = ANCA-associated vasculitides, SD = standard deviation, GU = genitourinary, ENT = ear nose and throat, OR = odds ratio, CI = confidence interval.

Abstract Image

肉芽肿病伴多血管炎的眼部和眼眶表现:对已发表病例的系统回顾。
目的:肉芽肿性多血管炎(GPA)是一种自身免疫性疾病,其特征是中小血管坏死性肉芽肿性炎症。这篇系统综述旨在强调最常见的眼科表现,并揭示它们与抗中性粒细胞胞浆抗体(ANCA)阳性和肉芽肿存在的关系。方法:从期刊创刊到2021年3月21日,在PubMed、Web of Science和Scopus电子数据库中检索病例报告和一系列眼科GPA。针对许多眼科体征和症状分析细胞质ANCA(c-ANCA)、核周ANCA(p-ANCA)和肉芽肿。对306例GPA患者进行了回顾性研究。结果:在我们的样本中,有47.7%的样本存在肉芽肿,有59.2%的样本存在c-ANCA,有10.8%的样本存在p-ANCA。眼分泌物、巩膜上炎、眼球突出和中枢神经系统(CNS)受累均与c-ANCA阳性几率较低显著相关。眼眶质量与p-ANCA阳性几率较低显著相关。中枢神经系统受累与p-ANCA阳性的几率较高显著相关(OR:3.08,95%CI:1.02,9.36,p=0.047),眼眶质量与p-ANCA阳性的几率较低显著相关。结论:我们建议临床医生在出现非特异性眼部主诉(如视力受损、眼眶肿块或眼球突出)的患者中考虑眼部或眼眶GPA,并进行进一步评估,以确定肉芽肿、c-ANCA或p-ANCA的可能存在。缩写:GPA=伴多血管炎的肉芽肿,ANCA=抗中性粒细胞胞质抗体,c-ANCA=胞质ANCA,p-ANCA=核周ANCA,CNS=中枢神经系统,AAVs=ANCA相关血管炎,SD=标准差,GU=泌尿生殖系统,ENT=耳鼻喉,OR=比值比,CI=置信区间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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