Takeuchi Masaru, Harimoto Kozo, Taguchi Manzo, Sakurai Yutaka
Department of Ophthalmology, National Defense Medical College, 3-2 Namiki, Tokorozawa City, Saitama, 359-8513, Japan.
BMC Ophthalmol. 2015 Dec 12;15:177. doi: 10.1186/s12886-015-0162-4.
Behçet's disease (BD)-associated uveitis causes retinal damage leading to severe visual disturbance. The early morphological changes in the retina are revealed by disappearance or disruption of the external limiting membrane (ELM), inner segment ellipsoid zone (EZ) and cone interdigitation zone (CIZ) in the outer retina shown on spectral domain-optical coherence tomography (SD-OCT). However, it is unknown whether these changes in the retina are reversible in BD-associated uveitis.
A 38-year-old man was referred to our hospital with 5 years history of panuveitis in both eyes. Recurrent oral ulcer, folliculitis, and genital ulcer were noted as systemic complications. Moderate cell infiltration into the anterior chamber, and diffuse vitritis were observed in both eyes, and best corrective visual acuity (BCVA) was 20/60 in the right and 20/200 in the left eye. Fluorescein angiography (FA) showed severe dye leakage from extensive retinal vessels in both eyes. Spectral domain-optical coherence tomography (SD-OCT) revealed retinal cysts and disruption of the external limiting membrane (ELM), inner segment ellipsoid zone (EZ) and cone interdigitation zone (CIZ) in the macular region of both eyes. BD was diagnosed based on the ocular features and systemic lesions, and infliximab therapy was initiated for the severe visual disturbance. After treatment with infliximab, foveal excavation was first recovered with disappearance of retinal cysts, and then ELM and EZ were gradually reconstituted on SD-OCT. Finally, CIZ became distinguishable after 24 months of infliximab therapy. BCVA was recovered to 20/25 in both eyes, and ocular inflammatory attack did not recur after the initiation of infliximab therapy.
Disruption of ELM, EZ, and CIZ shown on SD-OCT in BD-associated uveitis could be reconstituted by continuous infliximab treatment, which leaded to the improvement of visual acuity.
白塞病(BD)相关性葡萄膜炎可导致视网膜损伤,进而引起严重的视力障碍。光谱域光学相干断层扫描(SD - OCT)显示,视网膜外层的外限制膜(ELM)、内节椭圆体带(EZ)和视锥细胞指状交叉带(CIZ)消失或破坏,提示视网膜早期形态学改变。然而,BD相关性葡萄膜炎患者视网膜的这些改变是否可逆尚不清楚。
一名38岁男性因双眼全葡萄膜炎5年病史转诊至我院。患者有复发性口腔溃疡、毛囊炎和生殖器溃疡等全身并发症。双眼均可见中度前房细胞浸润和弥漫性玻璃体炎,右眼最佳矫正视力(BCVA)为20/60,左眼为20/200。荧光素血管造影(FA)显示双眼广泛视网膜血管严重染料渗漏。光谱域光学相干断层扫描(SD - OCT)显示双眼黄斑区视网膜囊肿以及外限制膜(ELM)、内节椭圆体带(EZ)和视锥细胞指状交叉带(CIZ)破坏。根据眼部特征和全身病变诊断为BD,并因严重视力障碍开始使用英夫利昔单抗治疗。英夫利昔单抗治疗后,首先视网膜囊肿消失,黄斑中心凹凹陷恢复,随后SD - OCT显示ELM和EZ逐渐重建。最终,英夫利昔单抗治疗24个月后CIZ变得清晰可辨。双眼BCVA恢复至20/25,英夫利昔单抗治疗开始后眼部炎症未复发。
BD相关性葡萄膜炎患者SD - OCT显示的ELM、EZ和CIZ破坏可通过持续英夫利昔单抗治疗得以重建,从而提高视力。