Wang Yu Tung, Tadarati Mongkol, Scholl Hendrik P, Bressler Neil M
*Retina Division, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland; and †Department of Ophthalmology, Rajavithi Hospital, College of Medicine, Rangsit University, Bangkok, Thailand.
Retin Cases Brief Rep. 2016 Winter;10(1):63-71. doi: 10.1097/ICB.0000000000000207.
To describe visual acuity changes associated with several cycles of accumulation, disappearance, and reaccumulation of vitelliform material in Best disease, with fundus photographs, fluorescein angiograms, and optical coherence tomography images documenting these stages.
Case report with 70 months of follow-up using fundus photography, fluorescein angiography, and optical coherence tomography to image the retina. A non-Hispanic white 33-year-old man with Best disease (positive for a mutation in the BEST1 gene, namely p.Tyr167Cys:c.500A>G).
The patient had a history of choroidal neovascularization (CNV) followed by scarring of the macula with sustained vision loss of ∼20/250 in the left eye when he was in his twenties. He subsequently presented in his thirties with acute vision loss in the right eye 3 times during a 70-month follow-up period. Each episode of vision loss in the right eye was preceded by several months of reaccumulation of vitelliform material in the macula apparent on fundus photographs, fluorescein angiograms, and optical coherence tomography, but no evidence of CNV on presentation. Each of the three episodes of vision loss in the right eye was followed by spontaneous gradual improvement in visual acuity over the next several months, correlating with decreasing amounts of the vitelliform material on clinical examination and fundus photographs. After the third documented recovery of visual acuity, at a time of stable vision, the patient developed CNV in the right eye, treated with intravitreal ranibizumab.
This case demonstrates that vitelliform material can reaccumulate and resorb several times in Best disease, with temporary visual acuity decline after each episode of vitelliform material accumulation. There is a need for continued vigilance for the development of CNV in patients presenting with acute vision loss, although this patient developed CNV at a time of stable vision.
通过眼底照片、荧光素血管造影和光学相干断层扫描图像记录这些阶段,描述与贝斯特病中玻璃膜疣状物质的几个积累、消失和再积累周期相关的视力变化。
病例报告,随访70个月,使用眼底摄影、荧光素血管造影和光学相干断层扫描对视网膜进行成像。一名33岁非西班牙裔白人男性患有贝斯特病(BEST1基因存在p.Tyr167Cys:c.500A>G突变)。
该患者有脉络膜新生血管(CNV)病史,随后黄斑形成瘢痕,20多岁时左眼视力持续丧失至约20/250。他在30多岁时,在70个月的随访期间右眼急性视力丧失3次。右眼每次视力丧失发作前,眼底照片、荧光素血管造影和光学相干断层扫描显示黄斑区玻璃膜疣状物质有几个月的再积累,但就诊时无CNV证据。右眼三次视力丧失发作后,接下来几个月视力均自发逐渐改善,这与临床检查和眼底照片上玻璃膜疣状物质数量减少相关。在第三次记录的视力恢复后,在视力稳定时,患者右眼发生CNV,接受了玻璃体内注射雷珠单抗治疗。
该病例表明,在贝斯特病中玻璃膜疣状物质可多次再积累和吸收,每次玻璃膜疣状物质积累后视力会暂时下降。对于出现急性视力丧失的患者,尽管该患者在视力稳定时发生了CNV,但仍需持续警惕CNV的发生。