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玻璃体内注射抗血管内皮生长因子治疗眼组织胞浆菌病脉络膜新生血管化

Intravitreal anti-vascular endothelial growth factor for choroidal neovascularization in ocular histoplasmosis.

作者信息

Hu Jennifer, Hoang Quan V, Chau Felix Y, Blair Michael P, Lim Jennifer I

机构信息

Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois.

出版信息

Retin Cases Brief Rep. 2014 Winter;8(1):24-9. doi: 10.1097/ICB.0b013e3182a48bcc.

DOI:10.1097/ICB.0b013e3182a48bcc
PMID:25372202
Abstract

PURPOSE

To report eight cases of long-term successful treatment of choroidal neovascularization because of ocular histoplasmosis syndrome with intravitreal anti-vascular endothelial growth factor agents.

METHODS

Retrospective case series. This article reviewed the course of eight eyes in seven patients who underwent intravitreal injection of bevacizumab and/or ranibizumab for treatment of choroidal neovascularization secondary to ocular histoplasmosis syndrome. Outcomes were assessed using pre- and post-anti-vascular endothelial growth factor visual acuities.

RESULTS

Eight eyes in seven patients were found to have new ocular histoplasmosis syndrome-associated subfoveal choroidal neovascularization lesions, as evidenced on clinical examination, fluorescein angiography, and optical coherence tomography. Intravitreal anti-vascular endothelial growth factor injections were used as initial or early treatment with successful resolution of the choroidal neovascularization lesions in most cases. Mean visual acuity improved from 20/60 to 20/47 over an average of 121.4 weeks. Either bevacizumab or ranibizumab was administered with an average of 2.6 injections per year of follow-up. Three eyes (37.5%) experienced a gain in visual acuity with a mean increase of 7.7 lines, 1 eye (12.5%) experienced no change, and 2 eyes (25%) experienced a loss of visual acuity of 2 or more lines. Six eyes (75%) were able to avoid mild visual loss (2 lines or less).

CONCLUSIONS

Intravitreal anti-vascular endothelial growth factor agents may successfully treat or at least stabilize neovascular complications of ocular histoplasmosis syndrome when used as a first-line treatment.

摘要

目的

报告8例因眼组织胞浆菌病综合征导致的脉络膜新生血管化经玻璃体内抗血管内皮生长因子药物长期成功治疗的病例。

方法

回顾性病例系列研究。本文回顾了7例患者8只眼的病程,这些患者接受了玻璃体内注射贝伐单抗和/或雷珠单抗治疗继发于眼组织胞浆菌病综合征的脉络膜新生血管化。使用抗血管内皮生长因子治疗前后的视力评估结果。

结果

7例患者的8只眼被发现有新的与眼组织胞浆菌病综合征相关的黄斑下脉络膜新生血管病变,临床检查、荧光素血管造影和光学相干断层扫描均证实了这一点。玻璃体内抗血管内皮生长因子注射被用作初始或早期治疗,大多数病例中脉络膜新生血管病变成功消退。平均视力在平均121.4周内从20/60提高到20/47。随访期间每年平均注射贝伐单抗或雷珠单抗2.6次。3只眼(37.5%)视力提高,平均提高7.7行;1只眼(12.5%)视力无变化;2只眼(25%)视力下降2行或更多。6只眼(75%)能够避免轻度视力丧失(2行或更少)。

结论

玻璃体内抗血管内皮生长因子药物作为一线治疗时,可成功治疗或至少稳定眼组织胞浆菌病综合征的新生血管并发症。

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