Biofluid, Tissue and Solid Mechanics for Medical Applications, Institute Biomedical Technology, Department of Electronics and Information Systems, iMinds Future Health Department, Ghent University, Gent, Belgium.
J Anat. 2014 Apr;224(4):509-17. doi: 10.1111/joa.12156. Epub 2014 Jan 17.
Although a full understanding of the hepatic circulation is one of the keys to successfully perform liver surgery and to elucidate liver pathology, relatively little is known about the functional organization of the liver vasculature. Therefore, we materialized and visualized the human hepatic vasculature at different scales, and performed a morphological analysis by combining vascular corrosion casting with novel micro-computer tomography (CT) and image analysis techniques. A human liver vascular corrosion cast was obtained by simultaneous resin injection in the hepatic artery (HA) and portal vein (PV). A high resolution (110 μm) micro-CT scan of the total cast allowed gathering detailed macrovascular data. Subsequently, a mesocirculation sample (starting at generation 5; 88 × 68 × 80 mm³) and a microcirculation sample (terminal vessels including sinusoids; 2.0 × 1.5 × 1.7 mm³) were dissected and imaged at a 71-μm and 2.6-μm resolution, respectively. Segmentations and 3D reconstructions allowed quantifying the macro- and mesoscale branching topology, and geometrical features of HA, PV and hepatic venous trees up to 13 generations (radii ranging from 13.2 mm to 80 μm; lengths from 74.4 mm to 0.74 mm), as well as microvascular characteristics (mean sinusoidal radius of 6.63 μm). Combining corrosion casting and micro-CT imaging allows quantifying the branching topology and geometrical features of hepatic trees using a multiscale approach from the macro- down to the microcirculation. This may lead to novel insights into liver circulation, such as internal blood flow distributions and anatomical consequences of pathologies (e.g. cirrhosis).
虽然全面了解肝脏循环是成功进行肝脏手术和阐明肝脏病理学的关键之一,但人们对肝脏脉管系统的功能组织知之甚少。因此,我们通过血管腐蚀铸型与新型微计算机断层扫描(CT)和图像分析技术相结合,实现并可视化了人体肝脏脉管系统的不同尺度,并进行了形态学分析。通过同时向肝动脉(HA)和门静脉(PV)内注入树脂,获得了人体肝脏血管腐蚀铸型。对整个铸型进行高分辨率(110μm)微 CT 扫描,可收集详细的大血管数据。随后,对中循环样本(从第 5 代开始;88×68×80mm³)和微循环样本(包括窦状隙在内的终末血管;2.0×1.5×1.7mm³)进行解剖和以 71μm 和 2.6μm 的分辨率成像。分割和 3D 重建允许定量分析 HA、PV 和肝静脉树的宏观和中观分支拓扑结构以及几何特征,直到第 13 代(半径范围为 13.2mm 至 80μm;长度范围为 74.4mm 至 0.74mm),以及微血管特征(平均窦状隙半径为 6.63μm)。结合腐蚀铸型和微 CT 成像,使用从宏观到微循环的多尺度方法可以定量分析肝树的分支拓扑结构和几何特征。这可能会深入了解肝脏循环,例如内部血流分布和病理学(如肝硬化)的解剖学后果。