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本文引用的文献

1
Mast cells in cutaneous tumors: innocent bystander or maestro conductor?皮肤肿瘤中的肥大细胞:无辜旁观者还是指挥大师?
Int J Dermatol. 2014 Jul;53(7):806-11. doi: 10.1111/j.1365-4632.2012.05745.x. Epub 2013 Apr 28.
2
β1-Adrenoceptor mRNA level reveals distinctions between infantile hemangioma and vascular malformations.β1-肾上腺素能受体 mRNA 水平揭示了婴幼儿血管瘤与血管畸形之间的区别。
Pediatr Res. 2013 Apr;73(4 Pt 1):409-13. doi: 10.1038/pr.2013.16. Epub 2013 Jan 31.
3
Preliminary experience on treatment of infantile hemangioma with low-dose propranolol in China.中国低剂量普萘洛尔治疗婴幼儿血管瘤的初步经验。
Eur J Pediatr. 2013 May;172(5):653-9. doi: 10.1007/s00431-012-1928-9. Epub 2013 Jan 23.
4
Pericytes from infantile hemangioma display proangiogenic properties and dysregulated angiopoietin-1.婴儿血管瘤中的周细胞表现出促血管生成特性和血管生成素-1 失调。
Arterioscler Thromb Vasc Biol. 2013 Mar;33(3):501-9. doi: 10.1161/ATVBAHA.112.300929. Epub 2013 Jan 3.
5
The role of β-adrenergic receptor signaling in the proliferation of hemangioma-derived endothelial cells.β-肾上腺素能受体信号在血管瘤衍生内皮细胞增殖中的作用。
Cell Div. 2013 Jan 3;8(1):1. doi: 10.1186/1747-1028-8-1.
6
CD133 selected stem cells from proliferating infantile hemangioma and establishment of an in vivo mice model of hemangioma.CD133 分选增殖期婴幼儿血管瘤干细胞及其在体动物模型的建立。
Chin Med J (Engl). 2013 Jan;126(1):88-94.
7
Orchestral actions of angiopoietin-1 in vascular regeneration.血管生成素-1 在血管再生中的交响乐作用。
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8
Copy number variation analysis in 98 individuals with PHACE syndrome.98 例 PHACE 综合征个体的拷贝数变异分析。
J Invest Dermatol. 2013 Mar;133(3):677-684. doi: 10.1038/jid.2012.367. Epub 2012 Oct 25.
9
E-selectin mediates stem cell adhesion and formation of blood vessels in a murine model of infantile hemangioma.E-选择素介导了幼年型血管瘤小鼠模型中的干细胞黏附和血管形成。
Am J Pathol. 2012 Dec;181(6):2239-47. doi: 10.1016/j.ajpath.2012.08.030. Epub 2012 Oct 4.
10
VEGF-directed blood vessel patterning: from cells to organism.血管内皮生长因子导向的血管模式形成:从细胞到机体。
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婴儿血管瘤的发病机制。

Pathogenesis of infantile haemangioma.

机构信息

The Department of Dermatology, Sheba Medical Center, Ramat-Gan 52621, Israel.

出版信息

Br J Dermatol. 2013 Jul;169(1):12-9. doi: 10.1111/bjd.12435.

DOI:10.1111/bjd.12435
PMID:23668474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3707963/
Abstract

Haemangioma is a vascular tumour of infancy that is well known for its rapid growth during the first weeks to months of a child's life, followed by a spontaneous but slow involution. During the proliferative phase, the vessels are disorganized and composed of immature endothelial cells. When the tumour involutes, the vessels mature and enlarge but are reduced in number. Fat, fibroblasts and connective tissue replace the vascular tissue, with few, large, feeding and draining vessels evident. Both angiogenesis and vasculogenesis have been proposed as mechanisms contributing to the neovascularization in haemangioma tumours. In recent years, several of the 'building blocks', the cells comprising the haemangioma, have been isolated. Among them are haemangioma progenitor/stem cells, endothelial cells and pericytes. This review focuses on these cell types, and the molecular pathways within these cells that have been implicated in driving the pathogenesis of infantile haemangioma.

摘要

血管瘤是一种婴儿期的血管肿瘤,其特征是在儿童生命的最初几周至几个月内迅速生长,随后自发但缓慢地退化。在增殖期,血管排列紊乱,由不成熟的内皮细胞组成。当肿瘤退化时,血管成熟并增大,但数量减少。脂肪、成纤维细胞和结缔组织取代血管组织,可见少量大的供养和引流血管。血管生成和血管发生都被认为是导致血管瘤新生血管形成的机制。近年来,已经分离出几种“构建块”,即组成血管瘤的细胞。其中包括血管瘤祖细胞/干细胞、内皮细胞和成纤维细胞。这篇综述重点介绍了这些细胞类型,以及这些细胞内的分子途径,这些途径被认为与婴儿血管瘤的发病机制有关。