女性静脉曲张疼痛的形态特征:紊乱的胶原蛋白和内皮细胞的可能作用

Shivani Thakur BA , Jasmin Dominguez Cervantes BS , Ahmed Zabiba BS
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引用次数: 0

摘要

本研究旨在探讨小静脉疼痛患者与大静脉疼痛症状性静脉曲张(VVs)患者的静脉壁厚度、胶原排列、肌肉层分布、内皮细胞排列的免疫组化表现以及静脉外膜层位置的差异程度。方法本研究于 2022 年 6 月至 2022 年 9 月在农村静脉科门诊诊所 Valley Vein Health Center 进行。从三名受试者中各采集了 10 个样本(n = 3):其中 5 个是症状较轻的小静脉,5 个是症状较重的大静脉。所有组织块都被横向切割成 5 微米厚的切片,垂直于血管轴线。选择了三种染色方法:马森三色染色法、苏木精和伊红染色法以及分化簇 31(CD31)染色法。使用 GraphPad 统计程序进行统计分析。结果小静脉的平均厚度小于大静脉(分别为 426 μm ± 26.1 μm vs 480 μm ± 19.2 μm;P <.001)。用苏木精、伊红和三色染色法对无症状的小静脉进行组织学和免疫组化(CD31)分析,结果显示内皮层覆盖在介质上,大部分是弹性组织纤维和平滑肌束。CD31 表达分析显示,与较小的血管相比,增大的静脉中膜有更多的内皮通道。大静脉的显微结构多变,胶原排列不规则,弹性蛋白层呈团块状,肌肉层呈羽毛状分布,血管外膜层增厚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Morphologic characteristics of painful varicose veins in women: possible role of disordered collagen and endothelial cells

Objective

This study examines to what extent vein wall thickness, collagen arrangements, muscular layers distribution, immunohistochemical presentation of endothelial cell arrangement, and adventitia layer placement differed in patients with small painful veins vs large painful symptomatic varicose veins (VVs).

Methods

This study was conducted from June 2022 to September 2022 at Valley Vein Health Center, a rural phlebology outpatient clinic. Ten samples from each of the three subjects were collected (n = 3): five were small symptomatic veins, and five were large symptomatic veins. All tissue blocks were cut transversely, perpendicular to the vessel axis, into 5-μm-thick sections. Three stains were chosen: Masson trichrome, hematoxylin and eosin, and a cluster of differentiation 31 (CD31). Statistical analysis was performed with the GraphPad statistical program. Comparisons between vein wall thicknesses were made using Student’s t test.

Results

The average thickness of small veins was less than that of large veins (426 μm ± 26.1 μm vs 480 μm ± 19.2 μm, respectively; P < .001). Histologic and immunohistochemical (CD31) analysis of small symptomatic VVs by hematoxylin and eosin and trichrome stain showed an endothelial layer overlying the media, mostly of elastic tissue fibers, and smooth muscle bundles. CD31 expression analysis demonstrated more endothelial channels in the tunica media of the enlarged veins compared with smaller vessels. The larger vein’s microscopic structure was variable with irregular collagen arrangement, clumped elastin layer appearance, feathered muscular layer distribution, and thickened adventitia layer placement.

Conclusions

The morphological distinctions in VVs highlighted in this study need to be considered to develop potential drug therapies tailored to women.

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