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与高血压性视网膜病变和类Purtscher样视网膜病变相关的C3肾小球病

C3 glomerulopathy associated with both hypertensive retinopathy and purtscher-like retinopathy.

作者信息

Zaidi Moosa, Mishra Kapil, Nguyen Huy Vu, Miller Paul Peter, Ghoraba Hashem, Karaca Irmak, Matsumiya Wataru, Nguyen Quan Dong, Leung Loh-Shan Bryan

机构信息

Department of Ophthalmology, Byers Eye Institute, Stanford University School of Medicine, 2452 Watson Court, Palo Alto, CA, 94303, USA.

Department of Pathology, Stanford University School of Medicine, Lane Building, L235, 300 Pasteur Drive, Stanford, CA, 94305, USA.

出版信息

Am J Ophthalmol Case Rep. 2022 Aug 6;27:101683. doi: 10.1016/j.ajoc.2022.101683. eCollection 2022 Sep.

Abstract

PURPOSE

This article reports the case of a 21-year-old woman with both hypertensive retinopathy and Purtscher-like retinopathy in association with C3 glomerulopathy.

OBSERVATIONS

The patient was referred for bilateral painless vision loss with posterior pole cotton wool spots, optic disc edema, and confluent retinal whitening suggesting a mixed picture of hypertensive retinopathy, with initial blood pressure 236/152, and Purtscher-like retinopathy. She was subsequently diagnosed with C3 glomerulopathy which likely caused her severe hypertension and which likely occurred alongside Purtscher-like retinopathy due to a shared pathogenesis of complement dysregulation. Follow up examination and imaging revealed gradual improvement in visual acuity, almost complete resolution of fundus exam abnormalities, improvement in macular nonperfusion, resolution of disc leakage and choroidal leakage, resolution of macular edema, and residual outer retinal hyperreflective foci in both eyes.

CONCLUSION AND IMPORTANCE

This case represents the first report of both Purtscher-like retinopathy and hypertensive retinopathy occurring in association with C3 glomerulopathy. It supports investigation of anti-complement therapy as a potential treatment for Purtscher-like retinopathy.

摘要

目的

本文报告了一名21岁女性患者的病例,该患者患有高血压性视网膜病变和类似Purtscher样视网膜病变,并伴有C3肾小球病。

观察结果

该患者因双侧无痛性视力丧失就诊,后极部有棉絮斑、视盘水肿和融合性视网膜变白,提示为高血压性视网膜病变的混合表现,初始血压为236/152,同时伴有类似Purtscher样视网膜病变。她随后被诊断为C3肾小球病,该病可能导致了她的严重高血压,并且由于补体调节异常的共同发病机制,可能与类似Purtscher样视网膜病变同时发生。随访检查和影像学显示视力逐渐改善,眼底检查异常几乎完全消退,黄斑无灌注改善,视盘渗漏和脉络膜渗漏消退,黄斑水肿消退,双眼均残留视网膜外层高反射灶。

结论与意义

本病例是首例同时出现类似Purtscher样视网膜病变和高血压性视网膜病变并伴有C3肾小球病的报告。它支持将抗补体治疗作为类似Purtscher样视网膜病变的潜在治疗方法进行研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7fc/9395975/1e43e90e6bba/gr1.jpg

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