gms | German Medical Science

67. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)
Joint Meeting mit der Koreanischen Gesellschaft für Neurochirurgie (KNS)

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

12. - 15. Juni 2016, Frankfurt am Main

The role of vasa vasorum activities in human carotid atherosclerosis is associated with plaque development and vulnerability

Meeting Abstract

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  • Sung-Pil Joo - Department of Neurosurgery, Chonnam National University Hospital, Korea
  • Tae Sun Kim - Department of Neurosurgery, Chonnam National University Hospital, Korea

Deutsche Gesellschaft für Neurochirurgie. 67. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), 1. Joint Meeting mit der Koreanischen Gesellschaft für Neurochirurgie (KNS). Frankfurt am Main, 12.-15.06.2016. Düsseldorf: German Medical Science GMS Publishing House; 2016. DocDI.05.04

doi: 10.3205/16dgnc121, urn:nbn:de:0183-16dgnc1214

Veröffentlicht: 8. Juni 2016

© 2016 Joo et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

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Objective: The aim of this study was to investigate the correlation between the activities of the carotid vasa vasorum and carotid plaque vulnerability using indocyanine green-video angiography (ICG-VA) during Carotid endarterectomy (CEA), focusing on how the carotid artery vasa vasorum is depicted.

Method: Sixty-nine patients who underwent CEA were enrolled prospectively from September 2013 to December 2014. ICG was injected intravenously as a bolus before and after resecting the atheroma during CEA. We also performed immunohistochemistry using CD68 (macrophage), CD117 (mast cell), CD4 (T-cell), and CD8 (T-cell) antibodies for resected plaque specimens.

Results: Active vasa vasorum density was observed in all patients on ICG-VA (n = 69). The vasa vasorum externa (VVE) and -interna (VVI) were seen in 11 (16%) and 57 patients (82.6%), respectively. The types of VVE were strongly associated with preoperative angiographic instability (90.0%, p = 0.005) and carotid plaque vulnerability (100%, p = 0.007) macroscopically. In contrast, the types of VVI were less associated with angiographic instability (36.1%) and plaque vulnerability (49.1%, p=0.003). CD68- and CD117-stained macrophages and mast cells were observed more frequently in unstable plaque, compared to those in stable plaque (p< 0.0001, p= 0.002, respectively.

Conclusions: The early appearance of VVE on ICG-VA was strongly associated with unstable carotid plaque and many microvessel channels that provided nutrients to the developing and expanding atheroma. Macrophages and mast cells were involved in the formation of microvessels in the unstable plaque phenotype.