Zusammenfassung
Myelitiden können idiopathisch, immunologisch vermittelt, nichtinfektiös und infektiös verursacht auftreten. Klinisch gibt es Gemeinsamkeiten, je nach Ätiologie, aber auch bedeutende Unterschiede. Die differenzialdiagnostische Abklärung der Ätiologie hat zentralen Stellenwert zur Therapieentscheidung und Abschätzung der Prognose. Im Folgenden wird im allgemeinen Teil auf gemeinsame epidemiologische, klinische, diagnostische und therapeutische Aspekte eingegangen, bevor im speziellen Teil die verschiedenen Myelitiden je nach Ätiologie dargestellt werden.
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Krämer, M., Berlit, P. (2018). Entzündliche Rückenmarkerkrankungen. In: Berlit, P. (eds) Klinische Neurologie. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-44768-0_69-1
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DOI: https://doi.org/10.1007/978-3-662-44768-0_69-1
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