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全身红斑狼疮和抗磷脂综合征继发黄斑水肿玻璃体内注射贝伐单抗后加重的毛细血管无灌注。

Aggravated capillary non-perfusion after intravitreal bevacizumab for macular edema secondary to systemic lupus erythematosus and anti-phospholipid syndrome.

机构信息

Department of Ophthalmology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Lupus. 2012 Mar;21(3):335-7. doi: 10.1177/0961203311422095. Epub 2011 Oct 5.

Abstract

A 22-year-old female with history of systemic lupus erythematosus (SLE) was referred for evaluation of decreased visual acuity in her right eye. Her best-corrected visual acuity (BCVA) at the time of presentation was 20/160. Widespread cotton wool spots and macular edema were seen on biomicroscopy. Fluorescein angiography (FA) revealed retinal arterial and venous obstruction with capillary nonperfusion at the superotemporal retina. Antiphospholipid syndrome (APS) was diagnosed based on positive lupus anti-coagulant and ocular manifestations. Scattered laser photocoagulation was applied at the nonperfusion area but the visual acuity continued to deteriorate due to macular edema. Intravitreal bevacizumab (IVB) was administered for macular edema. One day after IVB, the BCVA decreased to count fingers. FA revealed extended non-perfusion from the superotemporal area to the posterior pole. Use of intravitreal bevacizumab for macular edema secondary to SLE or APS should be considered carefully and patients monitored closely for vascular complications.

摘要

一位 22 岁的女性,有系统性红斑狼疮 (SLE) 病史,因右眼视力下降就诊。她就诊时的最佳矫正视力 (BCVA) 为 20/160。在生物显微镜下可见广泛的棉絮斑和黄斑水肿。荧光素血管造影 (FA) 显示视网膜动脉和静脉阻塞,上方视网膜有毛细血管无灌注。根据狼疮抗凝物阳性和眼部表现诊断为抗磷脂综合征 (APS)。在无灌注区进行了散在的激光光凝,但由于黄斑水肿,视力继续恶化。为黄斑水肿行玻璃体内注射贝伐单抗(IVB)。IVB 治疗后 1 天,BCVA 降至指数。FA 显示上方区域的无灌注范围扩展到后极。对于继发于 SLE 或 APS 的黄斑水肿,应慎重考虑使用玻璃体内注射贝伐单抗,并密切监测血管并发症。

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