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表现为双侧棉絮斑的巨细胞动脉炎

Giant Cell Arteritis Presenting as Bilateral Cotton Wool Spots.

作者信息

Fu Lanxing, O'Sullivan Eoin P

机构信息

Ophthalmology, King's College Hospital, London, GBR.

出版信息

Cureus. 2022 Oct 1;14(10):e29804. doi: 10.7759/cureus.29804. eCollection 2022 Oct.

DOI:10.7759/cureus.29804
PMID:36337822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9620483/
Abstract

An 81-year-old Afro-Caribbean woman presented with a two-week history of a dull headache in her temples, jaw claudication especially when chewing food, and reduced vision in her eyes, more pronounced in the right eye. There was no past medical or family history of hypothyroidism or autoimmunity. On examination, the vision was counting fingers in the right eye and 6/36 in the left eye, best corrected. Dilated fundus examination revealed multiple peripapillary cotton wool spots in both eyes though more pronounced in the right. Her erythrocyte sedimentation rate (ESR) was 120 mm/h, and her C-reactive protein (CRP) level was 79 mg/L. A temporal artery ultrasound scan was undertaken immediately which demonstrated a halo sign around both temporal arteries and so a giant cell arteritis (GCA) diagnosis was made. The patient was commenced on daily high-dose IV methylprednisolone 1 g for three days and referred to the rheumatology team. Her vision improved to 1/60 right and 6/9 left eye best corrected at three days post-treatment. At 12 months after the initial presentation, her vision stabilized at 6/60 in the right and 6/6 with complete visual fields in the left eye. Cotton wool spots can be a sign of GCA. Their appearance with or without characteristic systemic symptoms should prompt urgent evaluation.

摘要

一名81岁的非洲加勒比裔女性,出现双侧颞部钝痛两周,伴有咀嚼食物时的颌部跛行,以及视力下降,右眼更为明显。既往无甲状腺功能减退或自身免疫性疾病的病史及家族史。检查时,右眼视力为眼前指数,左眼最佳矫正视力为6/36。散瞳眼底检查发现双眼视乳头周围有多个棉絮斑,右眼更为明显。她的红细胞沉降率(ESR)为120mm/h,C反应蛋白(CRP)水平为79mg/L。立即进行了颞动脉超声扫描,结果显示双侧颞动脉周围有晕征,因此诊断为巨细胞动脉炎(GCA)。患者开始接受每日1g大剂量静脉注射甲基强的松龙治疗,为期三天,并转诊至风湿科团队。治疗三天后,她的右眼最佳矫正视力提高到1/60,左眼为6/9。初次就诊12个月后,她的右眼视力稳定在6/60,左眼视力为6/6,视野完整。棉絮斑可能是GCA的一个体征。无论有无典型的全身症状,其出现都应促使进行紧急评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/899c/9620483/e037de661b91/cureus-0014-00000029804-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/899c/9620483/890689cc46e6/cureus-0014-00000029804-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/899c/9620483/ee8377238c7c/cureus-0014-00000029804-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/899c/9620483/e037de661b91/cureus-0014-00000029804-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/899c/9620483/890689cc46e6/cureus-0014-00000029804-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/899c/9620483/ee8377238c7c/cureus-0014-00000029804-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/899c/9620483/e037de661b91/cureus-0014-00000029804-i03.jpg

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New-onset versus relapsing giant cell arteritis treated with tocilizumab: 3-year results from a randomized controlled trial and extension.新发病与复发巨细胞动脉炎应用托珠单抗治疗:一项随机对照试验和扩展研究的 3 年结果。
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Risk of Potential Glucocorticoid-Related Adverse Events in Patients with Giant Cell Arteritis: Results from a USA-Based Electronic Health Records Database.巨细胞动脉炎患者发生潜在糖皮质激素相关不良事件的风险:来自美国电子健康记录数据库的结果。
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Association of Giant Cell Arteritis With Race.巨细胞动脉炎与种族的关联。
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Seasonal incidence of biopsy-proven giant cell arteritis: a 20-year retrospective study of the University of California Davis Medical System.活检证实的巨细胞动脉炎的季节性发病:加利福尼亚大学戴维斯医疗系统 20 年回顾性研究。
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Does low risk of infections as a marker of effective immunity predict increased risk of subsequent giant cell arteritis or polymyalgia rheumatica? A Danish population-based case-control study.感染风险低作为有效免疫的标志是否预示着随后发生巨细胞动脉炎或风湿性多肌痛的风险增加?一项基于丹麦人群的病例对照研究。
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