Zusammenfassung
Das PZNSL macht etwa 2% aller intrakraniellen Tumoren aus. Histologisch handelt es sich ganz überwiegend um diffuse großzellige B-Zell-Lymphome. Von nodalen Lymphomen mit der gleichen Histologie unterscheidet sich das PZNSL durch seine starke ZNS-Affinität mit geringer Neigung zur systemischen Ausbreitung, sehr aggressiven Verlauf und ungewöhnliche Empfindlichkeit auf Hochdosismethotrexat (HDMTX). HDMTX ist daher das wichtigste Therapieelement bei PZNSL, wobei das optimale Protokoll aufgrund der Seltenheit der Erkrankung bisher nicht etabliert ist. Die wichtigsten Prognosefaktoren sind Alter und Allgemeinzustand. Bei jüngeren Patienten sollten intensivierte Chemotherapieprotokolle mit kurativem Behandlungsziel eingesetzt werden. Bei älteren Patienten ist eine Heilung meist nicht möglich, und die Therapie bedarf dringend einer Optimierung. Ein wichtiges Ziel bei allen Patienten mit PZNSL ist die Vermeidung einer potenziell schweren therapieassoziierten ZNS-Toxizität.
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Korfel, A., Schlegel, U. (2015). Primäre Zentralnervensystemlymphome (PZNSL). In: Adamietz, I., et al. Weiterbildung Onkologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-44835-9_13
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