首页> 外文期刊>International ophthalmology >Retinal fluorescein and indocyanine green angiography and optical coherence tomography in successive stages of Vogt-Koyanagi-Harada disease.
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Retinal fluorescein and indocyanine green angiography and optical coherence tomography in successive stages of Vogt-Koyanagi-Harada disease.

机译:Vogt-Koyanagi-Harada病连续阶段的视网膜荧光素和吲哚菁绿血管造影和光学相干断层扫描。

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Objective To report features of retinal fluorescein (FA) and indocyanine green (ICGA) angiography and optical coherence tomography (OCT) at successive stages of Vogt-Koyanagi-Harada (VKH) disease. Methods FA and ICGA were systematically performed in cases of VKH disease, at admission, 1 month later, and at the end of the follow-up. In addition, the most recent patients underwent OCT. In the follow-up, the clinical evolution and extent of treatment were related to the angiographic and tomographic features. Results FA and ICGA showed a diffuse delayed choroidal perfusion, including a delayed arterial, choriocapillar, and venous filling. This delayed choroidal perfusion involved the posterior pole and the hole periphery. The classically described serous retinal detachments were slowly filled from numerous pin points that could correspond to leakage through areas of damaged retinal pigment epithelium due to the choroidal ischemia. An uneven background choroidal fluorescence visible at the mid phase of ICGAwas the result of multiple hypofluorescent round lesions in the choroidal stroma. Choroidal folds appeared hypofluorescent in FA and hyperfluorescent in ICGA. Some of these angiographic findings were present at the very early neurologic stage of the disease. Moreover, under treatment, a persisting altered choroidal perfusion could increase the incidence of retinal detachment relapses. Discussion Various pathological conditions are characterized by choroidal involvement and serous retinal detachment. Angiographical findings may be helpful in the diagnosis. Conclusion FA coupled with ICGA can be an useful tool in the early diagnosis of VKH disease as well as during the tapering of immunosuppressive drugs.
机译:目的报道福格特-小柳市-原田病(VKH)疾病连续阶段的视网膜荧光素(FA)和吲哚菁绿(ICGA)血管造影和光学相干断层扫描(OCT)特征。方法在入院时,1个月后和随访结束时,对VKH病患者进行系统的FA和ICGA检查。另外,最近的患者接受了OCT。在随访中,临床进展和治疗范围与血管造影和断层扫描特征有关。结果FA和ICGA表现为弥漫性延迟脉络膜灌注,包括延迟动脉,脉络​​膜毛细血管和静脉充盈。这种延迟的脉络膜灌注涉及后极和孔的周围。古典描述的浆液性视网膜脱离是由许多针尖缓慢填充的,这些针尖可能对应于由于脉络膜局部缺血通过受损的视网膜色素上皮区域的渗漏。 ICGA中期可见的背景脉络膜荧光不均匀是脉络膜基质中多个次荧光圆形病变的结果。脉络膜褶皱在FA中显示为低荧光,在ICGA中显示为超荧光。这些血管造影结果中的一些表现在疾病的早期神经系统阶段。此外,在治疗下,持续的脉络膜灌注改变可能会增加视网膜脱离复发的发生率。讨论各种病理状况的特征是脉络膜受累和浆液性视网膜脱离。血管造影结果可能有助于诊断。结论FA结合ICGA可作为VKH疾病的早期诊断以及免疫抑制药物逐渐减少的有用工具。

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