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Spinale Tumoren

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Klinische Neurologie

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Zusammenfassung

Abhängig von der Lage im Spinalkanal werden intradurale und extradurale Tumoren unterschieden. Unter den extraduralen Tumoren sind Weichteiltumoren sowie primäre und sekundäre knöcherne Tumoren zu differenzieren. Intradurale Tumoren werden entsprechend ihrer Beziehung zum Rückenmark in intra- und extramedulläre Tumoren unterteilt. Es gibt zusätzliche Untergruppen: einige extramedulläre, intradurale Tumoren wachsen direkt durch die Dura hindurch oder entlang einer Nervenwurzel in den extraduralen Raum hinein. Es gibt exophytische intramedulläre Tumoren, die aus dem Rückenmark herauswachsen wie auch primäre extramedulläre Tumoren, die in das Rückenmark eindringen. Mit Ausnahme knöcherner Tumoren ist die weit überwiegende Zahl der spinalen Tumoren gutartig. Ein spinaler Tumor ist daher zuallererst eine chirurgisch zu behandelnde Erkrankung. Aussagen zur Prognose setzen eine Klärung der histologischen Diagnose voraus, die anhand der Klinik und der Bildgebung allenfalls näherungsweise getroffen werden kann.

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Correspondence to Jörg Klekamp .

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Klekamp, J. (2018). Spinale Tumoren. In: Berlit, P. (eds) Klinische Neurologie. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-44768-0_71-1

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  • DOI: https://doi.org/10.1007/978-3-662-44768-0_71-1

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