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Analyzing the human liver vascular architecture by combining vascular corrosion casting and micro-CT scanning: a feasibility study

机译:结合血管腐蚀铸模和显微CT扫描分析人体肝脏的血管结构:可行性研究

摘要

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).
机译:尽管对肝循环的充分了解是成功进行肝脏手术和阐明肝脏病理的关键之一,但对肝脏脉管系统的功能组织知之甚少。因此,我们物化并可视化了不同规模的人类肝血管,并通过将血管腐蚀铸件与新型微计算机断层扫描(CT)和图像分析技术相结合进行了形态分析。通过同时在肝动脉(HA)和门静脉(PV)中注入树脂,获得了人类肝脏血管腐蚀铸件。整个铸件的高分辨率(110microμm)显微CT扫描允许收集详细的大血管数据。随后,解剖了中循环样本(从第5代开始; 88×68×80mm³)和微循环样本(包括正弦波的末端血管; 2.0×1.5×1.7mm³)并以71μm和2.6μm的分辨率成像,分别。分割和3D重建可以量化宏观和中尺度分支拓扑结构,以及HA,PV和肝静脉树的几何特征,最多可生成13代(半径从13.2 13.mm至80μm;长度从74.4 mm至0.74 mm)。表现为微血管特征(平均正弦半径为6.63μm)。结合使用腐蚀铸造和微CT成像,可以使用从宏观到微循环的多尺度方法来量化肝树的分支拓扑和几何特征。这可能会导致对肝脏循环的新颖见解,例如内部血流分布和病理解剖学后果(例如肝硬化)。

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