眼科 ›› 2026, Vol. 35 ›› Issue (2): 109-113.doi: 10.13281/j.cnki.issn.1004-4469.2026.02.005

• 论著 • 上一篇    下一篇

孤立性盘周脉络膜炎临床特征分析

郝宏翔1   马雅1   彭晓燕1,2,3
  

  1. 1北京爱尔眼科医院,北京 100101; 2首都医科大学附属北京同仁医院 北京同仁眼科中心 眼科学与视觉科学北京市重点实验室,北京 100730; 3北京爱尔英智眼科医院,北京 100021

  • 收稿日期:2025-03-15 出版日期:2026-03-25 发布日期:2026-03-25
  • 通讯作者: 彭晓燕,Email: drpengxy@163.com

Analysis of clinical characteristics of solitary peripapillary choroiditis

Hao Hongxiang1, Ma Ya1, Peng Xiaoyan1,2,3   

  1. 1Beijing Aier Eye Hospital, Beijing 100101, China; 2Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Beijing 100730, China; 3Beijing Aier Yingzhi Eye Hospital, Beijing 100021, China
  • Received:2025-03-15 Online:2026-03-25 Published:2026-03-25
  • Contact: Peng Xiaoyan, Email: drpengxy@163.com

摘要:  目的  描述孤立性盘周脉络膜炎患者的临床及眼底影像学特征。设计  回顾性病例系列。研究对象  2013年6月至2025年1月就诊于北京同仁医院、北京爱尔眼科医院、北京爱尔英智眼科医院的孤立性盘周脉络膜炎患者6例(9眼),中位数年龄31岁,其中男性3例(3眼),女性3例(6眼),3例患者为双眼同时发病。方法  收集整理患者的临床资料,包括病史、全身情况及眼科检查资料,排除合并感染性疾病或自身免疫性疾病的病例。分析患者彩色眼底像、相干光断层扫描(OCT)、荧光素眼底血管造影(FFA)及吲哚青绿脉络膜血管造影(ICGA)的影像学资料并进行总结。随访时长1~48个月,平均13.1个月。主要指标  眼底影像的特征表现。结果  6例患者(9眼)眼底均表现为紧邻视盘一侧或围绕视盘的单一病灶。病灶范围及病变程度变化较大,其中3眼盘周视网膜色素变动、1眼视盘水肿、1眼盘周视网膜下黄白色渗出、5眼盘周视网膜下纤维增生膜、5眼继发脉络膜新生血管(CNV)并累及黄斑中心凹,伴有黄斑水肿及硬性渗出。9眼OCT表现均为盘周病灶区域视网膜色素上皮层(RPE)反射模糊且不连续,其下方脉络膜毛细血管层及中血管层萎缩,伴有视网膜外层结构破坏;其中5眼因继发视网膜下纤维化表现为视网膜下致密高反射,并因继发CNV表现为黄斑囊样水肿。行FFA及ICGA检查的4例患者(6眼)中,1眼FFA表现为早期盘周边界不清的稍高荧光,晚期荧光着染;5眼因继发CNV,FFA表现为盘周病灶内荧光渗漏,晚期荧光积存;ICGA检查中,6眼盘周病灶均表现为持续低荧光,病灶区脉络膜大血管影减少。结论  孤立性盘周脉络膜炎表现为紧邻视盘一侧或环形围绕视盘的单一脉络膜炎性病灶,主要累及RPE层、脉络膜毛细血管层及脉络膜中血管层,可继发视网膜下纤维化及CNV。

关键词: 脉络膜炎, 视网膜色素上皮, 脉络膜新生血管, 多模态影像

Abstract:  Objective To describe clinical and fundus imaging features of solitary peripapillary choroiditis patients. Design Retrospective case series. Participants Patients diagnosed as solitary peripapillary choroiditis in Beijing Tongren Hospital, Beijing Aier Eye Hospital and Beijing Aier Yingzhi Eye Hospital from June 2013 to January 2025. Six patients (9 eyes) with solitary peripapillary choroiditis were enrolled. There were 3 males (3 eyes) and 3 females (6 eyes) with the median age of 31 years. Three of them had binocular disease at onset of disease. Methods History of systemic comorbidities and results of systemic and ophthalmological examinations, including fundus photography, optical coherence tomography (OCT), fluorescein fundus angiography (FFA) and indocyanine green angiography (ICGA) were evaluated. Cases with infectious diseases or autoimmune diseases were excluded. Follow-up duration ranged from 1 month to 48 months, with an average of 13.1 months. Main Outcome Measures Characteristic signs of fundus imaging. Results In 9 eyes of the 6 patients, the lesion of solitary peripapillary choroiditis was unifocal, adjoining to one side of the optic disc, or surrounding the optic disc in all eyes. The area and severity of the lesion vary from peripapillary retinal pigment irregularity (3 eyes), to optic disc edema (1 eye), peripapillary subretinal yellow-whitish exudation (1 eye), and peripapillary subretinal fibrotic membrane (5 eyes), along with cystoid macular edema and macular hard exudates secondary to choroidal neovascularization (CNV) (5 eyes). In all the 9 eyes, OCT showed discontinuity and blurred reflection of retinal pigment epithelium, (RPE) with underlying choriocapillaris and choroidal Sattler layer atrophy, as well as destruction of the outer retina above. Furthermore, macular edema can be found when secondary CNV arose in 5 eyes. Four patients (6 eyes) received FFA and ICGA. FFA showed ill-defined slightly hyperfluorescent lesion temporally adjoining to optic disc in the early phase, and staining in late phase in 1 eye. In the rest 5 eyes, due to secondary CNV, the FFA showed fluorescence leakage inside the peripapillary lesion, and pooling in late phase. On ICGA of all 6 eyes, persistent hypofluorescence and reduce of choroidal large vessels were seen correspondingly. Conclusions The prominent fundus appearance of solitary peripapillary choroiditis is unifocal lesion adjoining to optic disc or surrounding optic disc. It is a kind of idiopathic choroiditis mainly affected RPE, choriocapillaris and choroidal Sattler layer. Secondary subretinal fibrosis and CNV can be seen.

Key words:  Choroiditis, Retinal pigment epithelium, Choroidal neovascularization, Multimodal imaging