Isolated cilioretinal artery occlusion secondary to perinuclear antineutrophil cytoplasmic antibody vasculitis

被引:1
作者
Mammo, Danny A. [1 ]
McClelland, Collin M. [1 ]
Chen, John [2 ,3 ]
Adams, Matthew K. [2 ]
Pulido, Jose [2 ]
Davies, John B. [4 ]
机构
[1] Univ Minnesota, Dept Ophthalmol & Visual Neurosci, Minneapolis, MN USA
[2] Mayo Clin, Dept Ophthalmol, Rochester, MN USA
[3] Mayo Clin, Dept Neurol, Rochester, MN USA
[4] VitreoRetinal Surg, PA, 7760 France Ave South,Suite 310, Edina, MN 55435 USA
关键词
Cilioretinal artery occlusion; antineutrophil cytoplasm antibody; vasculitis; microscopic polyangiitis; OCULAR MANIFESTATIONS; VASOSPASM;
D O I
10.1177/1120672119841541
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Introduction: Antineutrophil cytoplasm antibody-associated vasculitides encompass a diverse spectrum of autoimmune diseases characterized by necrotizing small vessel vasculitis. Ocular manifestations may be the presenting findings of antineutrophil cytoplasm antibody-associated vasculitides. Methods: Single, retrospective case study. Results: We report the rare case of a 55-year-old woman with a cilioretinal artery occlusion as the presenting feature of perinuclear antineutrophil cytoplasm antibody-associated microscopic polyangiitis. Conclusions: Although rare, antineutrophil cytoplasm antibody-related vasculitis should be considered in any retinal vascular occlusion, particularly in the setting of patients with new vague headaches and a paucity of vasculopathic risk factors.
引用
收藏
页码:NP53 / NP57
页数:5
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