【激光扫描检眼镜的红细胞荧光血管造影图像】。

J E Nasemann
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引用次数: 0

摘要

红细胞与荧光素结合在其表面,但在荧光素血管造影术中,红细胞不吸收细胞内的染料。因此,与血浆相比,这些细胞的荧光度较低。由于视网膜血管中红血球的高速运动,在常规血管造影中没有观察到这种现象。然而,扫描激光眼科检查允许视网膜成像具有非常高的时间分辨率。扫描激光束对单个红细胞的曝光时间仅为100纳秒。因此,扫描激光检眼镜允许成像快速移动的红细胞在大视网膜血管。病理性血流量减少清晰可见,可通过数字图像分析测量。3例血管闭塞患者的数值在0.1 ~ 1.8 mm/s之间。在循环完整的病例中,数字图像分析不足以测量红细胞速度。即使使用速度计对红细胞和移动的黑点进行半定量比较,叠加在血管造影上,也只能在红细胞速度降低的情况下获得可靠的结果。然而,对于临床医生来说,在扫描激光血管造影中观察红细胞流动是一种新的和迷人的工具。
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[Fluorescence angiography image of erythrocytes with the scanning laser ophthalmoscope].

Erythrocytes bind fluorescein to their surface, but they do not take up the dye intracellularly during fluorescein angiography. The cells are therefore hypofluorescent compared to blood plasma. Due to the high velocity of red blood cells in retinal vessels, this phenomenon has not been observed during conventional angiography. Scanning laser ophthalmoscopy, however, allows imaging of the retina with a very high temporal resolution. The exposure time of the scanning laser beam for a single erythrocyte is in the range of only 100 ns. Therefore, scanning laser ophthalmoscopy permits imaging of fast-moving red blood cells in large retinal vessels. Pathologically reduced blood flow is clearly visible and can be measured with digital image analysis. The values found in three patients with vascular occlusions were between 0.1 and 1.8 mm/s. In cases with intact circulation, digital image analysis was not sufficient to measure red blood cell velocity. Even if a velocimeter that permits semiquantitative comparison between erythrocytes and moving black dots is used, superimposed on the angiogram, reliable results can only be obtained in cases with reduced red cell velocity. Nevertheless, for the clinician observation of erythrocyte flow during scanning laser angiography is a new and fascinating tool.

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