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Saphenofemoral venous channels associated with recurrent varicose veins are not neovascular

El Wajeh, Y., Giannoukas, A.D., Gulliford, C.J., Suvarna, S.K., Chan, P. (2004) Saphenofemoral venous channels associated with recurrent varicose veins are not neovascular. European Journal of Vascular and Endovascular Surgery, 28 (6). pp. 590-594. ISSN 1078-5884. (doi:10.1016/j.ejvs.2004.09.011) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:78335)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
https://doi.org/10.1016/j.ejvs.2004.09.011

Abstract

Background. Recurrence of varicose veins after apparently adequate surgery is common. Neovascularisation, the formation of new vascular channels between a venous surgery site and new varicosities, is thought to be an important cause of recurrence. The aim of this study was to provide histological evidence of the 'neovascularisation' process. Method. Tissue samples from the region of the previously ligated saphenofemoral junction (SFJ) were taken from 14 limbs with recurrent varicose veins and from nine control limbs. Tissue samples were analysed histologically for overall vascularity, and the presence of intimal circular fibrosis, intimal eccentric fibrosis, medial thickened elastosis, and thrombosis in the microscopic thin walled vessels within the tissue. The same samples were analysed immunohistoligically for S100, a neural marker, and Ki-67 (Mib 1), a marker of endothelial proliferation. Absent S100 and positive Ki-67 were considered as evidence of new vessels. Result. No significant difference was found between the venous recurrence and control groups in respect to histological features. S100 positive nerve fibrils were seen associated with dilated venous channels in the majority of both redo and control groups (p=1, Fisher's exact test). Only one section stained positively with Ki-67 (Mib1) in a single vascular channel for a few endothelial cells. The remaining control and redo cases were negative for Mib 1 (p=1, Fisher's exact test). Conclusion. We found little evidence of neovascularisation associated with recurrent varicose veins in the saphenofemoral region. The venous channels that develop at the previously ligated SFJ may represent adaptive dilatation of pre-existing venous channels (vascular remodelling), probably in response to abnormal haemodynamic forces.

Item Type: Article
DOI/Identification number: 10.1016/j.ejvs.2004.09.011
Uncontrolled keywords: Histology, Neovascularisation, Recurrent varicose veins, biological marker, monoclonal antibody Ki 67, protein S 100, adult, aged, article, cell proliferation, clinical article, controlled study, elastosis, endothelium cell, femoral vein, Fisher exact test, histology, human, human cell, human tissue, immunohistology, neovascularization (pathology), neurofilament, priority journal, recurrent disease, saphenous vein, thrombosis, varicosis, vascular fibrosis, vascularization, vein dilatation, Adult, Aged, Endothelium, Vascular, Femoral Vein, Humans, Immunohistochemistry, Ki-67 Antigen, Middle Aged, Neovascularization, Pathologic, Recurrence, S100 Proteins, Saphenous Vein, Varicose Veins
Divisions: Divisions > Division of Natural Sciences > Kent and Medway Medical School
Depositing User: Philip Chan
Date Deposited: 07 Nov 2019 15:11 UTC
Last Modified: 05 Nov 2024 12:42 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/78335 (The current URI for this page, for reference purposes)

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