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Ultrastructural observations in port wine stains.

作者信息

Schneider B V, Mitsuhashi Y, Schnyder U W

机构信息

University Hospital of Zurich, Department of Dermatology, Switzerland.

出版信息

Arch Dermatol Res. 1988;280(6):338-45. doi: 10.1007/BF00426611.

DOI:10.1007/BF00426611
PMID:3190266
Abstract

The cause for the progressive vascular dilatation in port wine stains remains unclear. We compared the histology and ultrastructure of lesional and adjacent normal skin in paired biopsy specimens of 12 and 8 patients, respectively (age range, 6 to 53 years). In semithin sections, the lesions of all patients showed ectatic vessels and a fine-fibrous or hyaline thickening of the walls of postcapillary venules, as well as in some instances a loosening of the surrounding connective tissue. Ultrastructurally, the wall material consisted predominantly of peripheral deposits of amorphous material interspersed with collagen fibrils (diameter, 35 +/- 4 nm); occasionally the number of basal laminae in the inner part was also increased. Cross-banded filamentous aggregates with a periodicity of 95 nm were observed in and around the walls. The endothelium of many patients displayed fenestrations and/or small gaps. Various kinds of alterations of the intervascular connective tissue were found. We conclude that structural alterations of the vascular and later also of the intervascular connective tissue are related to the dilatation of the vessels. These findings are in agreement with the immunopathologically demonstrated increase of basement membrane components in the same biopsy specimens, but are interpreted as secondary phenomena. Endothelial stability and permeability may also be affected.

摘要

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本文引用的文献

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[On plane angiomas; naevi hyperaemici].[关于平面血管瘤;充血性痣]
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Int J Mol Sci. 2022 Oct 12;23(20):12139. doi: 10.3390/ijms232012139.
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Br J Dermatol. 2022 Nov;187(5):730-742. doi: 10.1111/bjd.21723. Epub 2022 Jul 31.
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Therapeutic Strategies for Untreated Capillary Malformations of the Head and Neck Region: A Systematic Review and Meta-Analyses.头颈部未治疗毛细血管畸形的治疗策略:系统评价和荟萃分析。
Am J Clin Dermatol. 2021 Sep;22(5):603-614. doi: 10.1007/s40257-021-00616-5. Epub 2021 Jun 23.
6
Development of a core outcome domain set for clinical research on capillary malformations (the COSCAM project).制定毛细血管畸形临床研究的核心结局领域集(COSCAM 项目)。
J Eur Acad Dermatol Venereol. 2021 Sep;35(9):1888-1895. doi: 10.1111/jdv.17376. Epub 2021 Jun 16.
7
Site-specific pharmaco-laser therapy: A novel treatment modality for refractory port wine stains.特定部位药物激光治疗:难治性葡萄酒色斑的一种新型治疗方式。
J Clin Transl Res. 2019 May 1;5(1):1-24. eCollection 2019 Sep 8.
8
The Pathogenesis of Port Wine Stain and Sturge Weber Syndrome: Complex Interactions between Genetic Alterations and Aberrant MAPK and PI3K Activation.葡萄酒色斑和脑面血管瘤病的发病机制:遗传改变与异常 MAPK 和 PI3K 激活之间的复杂相互作用。
Int J Mol Sci. 2019 May 7;20(9):2243. doi: 10.3390/ijms20092243.
9
Glucose in Conjunction with Multiple Laser Pulses on Laser Treatment of Port-wine Stain: An in vivo Study.葡萄糖联合多脉冲激光治疗鲜红斑痣的体内研究
Lasers Med Sci. 2018 Aug;33(6):1295-1306. doi: 10.1007/s10103-018-2481-1. Epub 2018 Mar 14.
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Coexistence of Eph receptor B1 and ephrin B2 in port-wine stain endothelial progenitor cells contributes to clinicopathological vasculature dilatation.Eph 受体 B1 和 Ephrin B2 在葡萄酒色斑内皮祖细胞中的共存有助于临床病理血管扩张。
Br J Dermatol. 2017 Dec;177(6):1601-1611. doi: 10.1111/bjd.15716. Epub 2017 Nov 16.
4
Capillary alterations in scleroderma.硬皮病中的毛细血管改变。
J Am Acad Dermatol. 1980 Feb;2(2):161-70. doi: 10.1016/s0190-9622(80)80396-3.
5
The nature and evolution of port wine stains: a computer-assisted study.葡萄酒色斑的本质与演变:一项计算机辅助研究。
J Invest Dermatol. 1980 Mar;74(3):154-7. doi: 10.1111/1523-1747.ep12535052.
6
Port wine stains and the response to argon laser therapy: successful treatment and the predictive role of color, age, and biopsy.葡萄酒色斑与氩激光治疗反应:成功的治疗以及颜色、年龄和活检的预测作用
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