Zusammenfassung
Zentrale vestibuläre Schwindelformen entstehen durch Läsionen entlang der vestibulären Verbindungen von den Vestibulariskernen in der Medulla oblongata zu den okulomotorischen Kernen und Integrationszentren im rostralen Mittelhirn sowie zum Vestibulozerebellum, Thalamus und vestibulären Kortex im temporoparietalen Großhirn (Brandt und Dieterich 1995). Es handelt sich oft um klar definierte klinische Syndrome unterschiedlicher Ätiologie, deren typische Befunde aus Okulomotorik, Wahrnehmung und Haltungsregulation eine topische Hirnstammdiagnostik erlauben. Die Analyse des Nystagmus kann für die lokalisatorische Zuordnung hilfreich sein (Büttner et al. 1995). Auf diese typischen Befunde soll hier eingegangen werden. Zentrale vestibuläre Syndrome können je nach Größe der Läsion isoliert vorkommen oder aber Teil eines komplexen infratentoriellen Syndroms sein, wobei als weitere Symptome supranukleäre oder nukleare Okulomotorikstörungen und/oder weitere neurologische Hirnstammausfälle vorkommen (z.B. Wallenberg-Syndrom mit „ocular tilt reaction“ sowie Horner-Syndrom, Sensibilitätsstörungen, Ataxie, Gaumensegelparese, Dysarthrophonie und Dysphagie).
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Brandt, T., Strupp, M., Dieterich, M. (2004). Zentrale vestibuläre Schwindelformen. In: Vertigo. Steinkopff, Heidelberg. https://doi.org/10.1007/978-3-662-13375-0_3
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DOI: https://doi.org/10.1007/978-3-662-13375-0_3
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