Department of Basic Medical Sciences, Faculty of Medicine, University of La Laguna, Tenerife, Spain.
Department of Pathology, Eurofins® Megalab-Hospiten Hospitals, Tenerife, Spain.
Histol Histopathol. 2021 Feb;36(2):217-228. doi: 10.14670/HH-18-292. Epub 2020 Dec 18.
Intussusceptive angiogenesis (IA) is the process by which pre-existing blood vessels split, expand and remodel through intravascular pillar formation. In previous works, we studied the morphologic characteristics of intravascular papillary endothelial hyperplasia (IPEH) and suggested the participation of IA in the histogenesis of the lesion. Our current goal is to demonstrate that myriad papillae in IPEH are in fact myriad pillars, the hallmarks of IA. For this purpose, specimens of 14 cases of IPEH were used for conventional histologic techniques, immunohistochemistry and immunofluorescence in confocal microscopy. The studies showed the following pillar characteristics: a) structural composition by an endothelial cell (EC) cover and a connective core, b) characteristic pillar image and its appearance and disappearance in whole-mounted and series of individual views in confocal microscopy (requirements for pillar identification), c) arrangement in masses, alignments and meshes, and d) formation from vein intimal ECs, which extend and originate loops that encircle vein wall components (interstitial tissue structures: ITSs) and fibrin. The encircling ECs form the pillar cover and the encircled ITSs or fibrin form the initial core. Intraluminal endothelial bridges also originate from the vessel wall and from the pillars (nascent and thin pillars). In conclusion, the formation of myriad pillars, predominantly in veins, is the basis of IPEH. This lesion may therefore be considered an excessive expression of IA: IA becomes a lesion.
腔内芽生血管生成(IA)是指血管内支柱形成导致预先存在的血管分裂、扩张和重塑的过程。在之前的研究中,我们研究了血管内乳头状内皮增生(IPEH)的形态特征,并提出了 IA 参与该病变的组织发生。我们目前的目标是证明 IPEH 中的无数乳突实际上是无数的支柱,这是 IA 的标志。为此,使用了 14 例 IPEH 标本进行常规组织学技术、免疫组织化学和共聚焦显微镜免疫荧光检查。研究表明,支柱具有以下特征:a)由内皮细胞(EC)覆盖和结缔核心组成的结构组成;b)特征性支柱图像及其在共聚焦显微镜的整体和系列单个视图中的出现和消失(支柱识别的要求);c)在团块、排列和网眼中的排列;d)从静脉内膜 EC 形成,这些 EC 延伸并形成环绕静脉壁成分(间质组织结构:ITS)和纤维蛋白的环。环绕的 EC 形成支柱覆盖物,环绕的 ITS 或纤维蛋白形成初始核心。腔内内皮桥也起源于血管壁和支柱(新生和薄支柱)。总之,众多支柱的形成,主要是在静脉中,是 IPEH 的基础。因此,该病变可被认为是 IA 的过度表达:IA 成为了病变。