gms | German Medical Science

65. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

11. - 14. Mai 2014, Dresden

Impact of endothelial tight junction alterations on cavernous malformation bleeding propensity

Meeting Abstract

  • Dejan Jakimovski - Klinik für Neurochirurgie, UniversitätsSpital Zürich; Klinik für Neurochirurgie, RWTH, Uniklinik Aachen
  • Hannah Schneider - Klinik für Neurochirurgie, UniversitätsSpital Zürich; Labor für Molekulare Neuro-Onkologie, UniversitätsSpital Zürich
  • Karl Frei - Klinik für Neurochirurgie, UniversitätsSpital Zürich; Labor für Molekulare Neuro-Onkologie, UniversitätsSpital Zürich
  • Lieven N. Kennes - Institut für Medizinische Statistik, RWTH, Uniklinik Aachen
  • Helmut Bertalanffy - Klinik für Neurochirurgie, UniversitätsSpital Zürich; International Neuroscience Institute, Hannover

Deutsche Gesellschaft für Neurochirurgie. 65. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC). Dresden, 11.-14.05.2014. Düsseldorf: German Medical Science GMS Publishing House; 2014. DocMO.02.02

doi: 10.3205/14dgnc002, urn:nbn:de:0183-14dgnc0020

Veröffentlicht: 13. Mai 2014

© 2014 Jakimovski et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.de). Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.


Gliederung

Text

Objective: Endothelial tight junction (TJ) expression in cerebral cavernous malformations (CCM) is mostly absent, which causes increased perilesional erythrocyte and fluid oozing. However, in a subset of CCM lesions, foci of preserved TJ staining are observed along endothelial cell contacts. We evaluated the clinical relevance of the focal TJ protein expression and the association with CCM bleeding propensity.

Method: Immunohistochemical staining for the TJ proteins claudin-5, occludin and ZO-1 was performed on 32 CCM specimens, surgically resected in the period 2008-2010. The patients were allocated in two groups according to TJ protein expression and the clinical and radiological parameters of aggressiveness were analyzed and compared.

Results: Complete absence was identified in 20 and focal TJ protein expression in 12 specimen. CCM’s with absent TJ immunoreactivity had significantly larger size (p=0.02) as well as higher propensity for development of frank hematomas (p=0.03) and perilesional edema (p=0.01). Symptom severity, multiplicity, DVA presence and CCM location did not show a significant difference depending on TJ expression.

Conclusions: In a univariate analysis we observed significantly lesser propensity for frank hematomas and perilesional edema as well as smaller size in CCM lesions with focal TJ expression. Although it cannot be used in predictive manner, the observed difference in TJ protein expression might be the rational for different bleeding propensity of the CCM lesions. This is a basis for further multivariate analyses of possible CCM biologic predictors.