肉芽肿合并多血管炎患者的非典型无痛性视力丧失。

GMS ophthalmology cases Pub Date : 2020-12-15 eCollection Date: 2020-01-01 DOI:10.3205/oc000173
Patricia C Nelson, Vamsi Kunam, Claudia Prospero Ponce
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引用次数: 1

摘要

血管炎是视力丧失的常见原因,通常是疼痛的。在成人最常见的原发性血管炎巨细胞动脉炎中,我们看到炎症标志物升高,肉芽肿性炎症,并伴有头痛或头皮压痛。肉芽肿性多血管炎(GPA)引起的视力丧失是罕见的,通常与疼痛和眼眶表现有关。我们的病人表现为呼吸短促和无痛性视力丧失,没有眼窝炎症或神经增强,眼底检查正常,提示后缺血性视神经病变。亚专科之间的合作和获得组织样本是诊断肉芽肿病合并多血管炎的关键,以确保及时治疗这种致命的致盲疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Atypical painless vision loss in a patient with granulomatosis with polyangiitis.

Atypical painless vision loss in a patient with granulomatosis with polyangiitis.

Vasculitis is a common cause of vision loss, and typically painful. In giant cell arteritis, the most common primary vasculitis in adults, we see elevated inflammatory markers, granulomatous inflammation, and associated headache or scalp tenderness. Vision loss caused by granulomatous with polyangiitis (GPA) is rare and typically associated with pain and orbital findings. Our patient presented for shortness of breath and painless vision loss without orbital inflammation or neural enhancement and a normal fundus exam, suggesting posterior ischemic optic neuropathy. Collaboration amongst sub-specialties and obtaining tissue samples are key to diagnosing granulomatosis with polyangiitis to ensure timely treatment of this fatal and blinding disease.

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