Haen Sebastian P, Spaide Richard F
Vitreous Retina Macula Consultants of New York, New York, New York, USA.
Am J Ophthalmol. 2008 May;145(5):847-53. doi: 10.1016/j.ajo.2008.01.008. Epub 2008 Mar 10.
To investigate the autofluorescence findings associated with multifocal choroiditis and panuveits (MCP), a condition that has marked potential to affect the retinal pigment epithelium (RPE).
Observational case series.
This is a retrospective review of consecutive patients with MCP examined in a retinal referral practice. Each patient was given a comprehensive examination including fundus photographs, angiographic studies, and autofluorescence photography with an excitation filter with the bandpass wavelengths of 535 to 585 nm and a barrier filter with a bandpass of 615 to 715 nm. Integrative analysis was performed of the ocular imaging to ascertain abnormalities caused by the disease.
Thirty-six eyes of 18 consecutive patients were evaluated. The mean duration of symptoms was 86.2 months and the mean visual acuity was 20/50. Of the 36 eyes, 23 had choroidal neovascularization (CNV). Chorioretinal hypoautofluorescent spots >or= 125 microns usually, but not always, had the clinically evident correlate of a punched-out scar visible by color fundus photography. Chorioretinal hypoautofluorescent spots less than 125 microns, which could number in the hundreds, typically were not visible by color fundus photography. All chorioretinal scars visible by color fundus photography were visible by autofluorescence photography. During follow-up many patients developed new clinically evident chorioretinal scars, which were presaged in earlier autofluorescence photographs. CNV had a hyperautofluorescent boundary, making it readily visible.
Patients with MCP have much more widespread involvement of the RPE than would be suspected by other means of imaging. Autofluorescence photography supplies information about inflammatory damage and secondary CNV in a noninvasive manner.
研究与多灶性脉络膜炎和全葡萄膜炎(MCP)相关的自发荧光表现,MCP这种病症具有显著影响视网膜色素上皮(RPE)的可能性。
观察性病例系列。
这是一项对在视网膜转诊诊所接受检查的连续性MCP患者的回顾性研究。每位患者均接受了全面检查,包括眼底照相、血管造影研究以及使用带通波长为535至585nm的激发滤光片和带通为615至715nm的阻挡滤光片进行的自发荧光照相。对眼部成像进行综合分析以确定由该疾病引起的异常。
对18例连续患者的36只眼进行了评估。症状的平均持续时间为86.2个月,平均视力为20/50。在这36只眼中,23只存在脉络膜新生血管(CNV)。脉络膜视网膜低自发荧光斑点≥125微米通常(但并非总是)在彩色眼底照相中具有可见的典型凿孔样瘢痕的临床明显对应表现。小于125微米的脉络膜视网膜低自发荧光斑点,其数量可达数百个,通常在彩色眼底照相中不可见。所有在彩色眼底照相中可见的脉络膜视网膜瘢痕在自发荧光照相中也可见。在随访期间,许多患者出现了新的临床明显的脉络膜视网膜瘢痕,这些瘢痕在早期的自发荧光照片中已有预示。CNV有一个高自发荧光边界,使其易于观察到。
MCP患者的RPE受累范围比通过其他成像方式所怀疑的要广泛得多。自发荧光照相以非侵入性方式提供有关炎症损伤和继发性CNV的信息。