首页> 外文期刊>Journal of cutaneous pathology >Myopericytoma and arterial intimal thickening: the relationship between myopericytes and myointimal cells.
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Myopericytoma and arterial intimal thickening: the relationship between myopericytes and myointimal cells.

机译:肌细胞瘤和动脉内膜增厚:肌细胞与肌内膜细胞之间的关系。

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摘要

BACKGROUND: Myopericytomas with intravascular growth have been reported and have been occasionally documented as intraarterial. In a retrospective study, we assessed intraarterial growth in myopericytomas, co-existence with arterial intimal thickening (IT) and the relationship between the two. METHODS: This retrospective study was undertaken using 11 myopericytomas evaluated in serial microscopical sections. The results in light microscopy, electron microscopy and immunohistochemistry [including alpha-smooth muscle actin (SMA), desmin and h-caldesmon] were evaluated. RESULTS: In four myopericytomas, we found intraarterial growth, with large areas of disrupted arterial wall and attachment of veins and venules, exhibiting angiogenic phenomena. Arterial IT was present and partially incorporated within the tumor (simulating medium-sized vessels). The neointimal (myointimal) cells shared morphological and immunohistochemical phenotype with the myopericytoma myoid cells, including alpha-SMA positivity and desmin negativity. Four of the remaining myopericytomas showed structures similar to arterial IT within the tumor. CONCLUSIONS: The findings shown here, including the association between myopericytomas and arterial IT, the incorporation of the latter into the tumor and the similar phenotype of their respective myoid and myointimal cells, support a close relationship between these processes. Histogenically, the pericytes of the penetrating neovasculature originating from the attached venules and veins may contribute to both lesions.
机译:背景:有血管内生长的肌细胞瘤已有报道,偶有文献记载为动脉内瘤。在一项回顾性研究中,我们评估了肌细胞瘤中的动脉内生长,与动脉内膜增厚(IT)并存以及两者之间的关系。方法:本回顾性研究是使用连续显微切片中评估的11种肌细胞瘤进行的。评估了光学显微镜,电子显微镜和免疫组织化学的结果[包括α-平滑肌肌动蛋白(SMA),结蛋白和h-caldesmon]。结果:在四个肌细胞瘤中,我们发现动脉内生长,大面积的动脉壁破裂以及静脉和小静脉的附着,表现出血管生成现象。存在动脉IT,并且部分纳入肿瘤内(模拟中型血管)。新内膜(肌内膜)细胞与肌细胞瘤肌样细胞共享形态学和免疫组织化学表型,包括α-SMA阳性和结蛋白阴性。剩下的四个肌细胞瘤显示出与肿瘤内动脉IT相似的结构。结论:这里显示的发现,包括肌细胞瘤和动脉IT之间的关联,后者掺入肿瘤中以及它们各自的肌样和肌内膜细胞的相似表型,都支持了这些过程之间的密切关系。从组织学上讲,起源于附着的小静脉和静脉的穿透性新脉管系统的周细胞可能对这两种病变都有影响。

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