Comparative microanatomy and histology of spinal and cerebral veins: Implications for dural arteriovenous fistula clinical presentations.

Cerebral veins Dural arteriovenous fistulas Hemorrhagic presentation Spinal veins

Journal

Tissue & cell
ISSN: 1532-3072
Titre abrégé: Tissue Cell
Pays: Scotland
ID NLM: 0214745

Informations de publication

Date de publication:
28 Oct 2024
Historique:
received: 18 09 2024
revised: 25 10 2024
accepted: 25 10 2024
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 31 10 2024
Statut: aheadofprint

Résumé

Cranial dural arteriovenous fistulas (DAVFs) that display cortical venous drainage are at risk of hemorrhage, unlike spinal DAVFs, which seldom bleed. The underlying mechanism for this difference is poorly understood. We hypothesized that cerebral veins are more fragile than spinal veins due to differences in histologic compositions. Thus, spinal and cerebral veins from five formalin-fixed human cadavers were examined through macroscopic and histological analysis, using hematoxylin, eosin and safran (HES), and orcein stains to compare them. Twenty-four cerebral veins and thirteen spinal veins were analyzed. The mean diameter of the cerebral veins was 1.02 ± 0.59 mm, while that of spinal veins was 0.52 ± 0.26 mm (p = 0.003). The mean thickness of cerebral veins was similar to their spinal counterparts (0.09 ± 0.07 mm vs 0.06 ± 0.02 mm; p = 0.12). The mean diameter-to-thickness ratio was 13.76 ± 6.05 mm for cerebral veins and 10.06 ± 7.23 mm for spinal veins (p = 0.023). In most of the analyzed vessels, the venous wall was composed of endothelial cells resting on layers of smooth muscle, separated by elastica lamina. Cerebral and spinal veins exhibit distinct calibers while maintaining comparable wall thicknesses, resulting in a greater diameter-to-thickness ratio for cerebral veins compared to spinal veins. This difference may after their resistance to pressure. Furthermore, variations in the transparietal pressure gradient between cranial and spinal subarachnoid space, along with differences in arterial blood flow through the fistulous veins, might contribute to the observed differences in clinical presentation.

Identifiants

pubmed: 39481222
pii: S0040-8166(24)00298-2
doi: 10.1016/j.tice.2024.102597
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102597

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest All authors declare: no support from any organization for this study; no financial relationships with any organizations that might have an interest in the submitted work.

Auteurs

Etienne Lefevre (E)

Department of Neurosurgery, APHP, Hôpital de la Pitié-Salpêtrière, Paris, France; Laboratory of Anatomy, University of Bordeaux, Bordeaux, France. Electronic address: etienne.lefevre@neurochirurgie.fr.

Mégane Le Quang (M)

Department of Pathology, University Hospital of Bordeaux, Place Amélie Raba-Léon, Bordeaux, France.

Vincent Jecko (V)

Laboratory of Anatomy, University of Bordeaux, Bordeaux, France; Neurosurgery Department A, Place Amélie Raba-Léon, Bordeaux, France.

Maxime Nogues (M)

Laboratory of Anatomy, University of Bordeaux, Bordeaux, France.

Dominique Liguoro (D)

Laboratory of Anatomy, University of Bordeaux, Bordeaux, France; Neurosurgery Department A, Place Amélie Raba-Léon, Bordeaux, France.

Franck Bielle (F)

Department of Neuropathology, APHP, Hôpital de la Pitié-Salpêtrière, Paris, France.

Paul Roblot (P)

Laboratory of Anatomy, University of Bordeaux, Bordeaux, France; University Hospital of Bordeaux, Place Amélie Raba-Léon, Bordeaux, France; Neurosurgery Department A, Place Amélie Raba-Léon, Bordeaux, France.

Classifications MeSH