Zusammenfassung
Es werden mindestens 15 histologische Subtypen unterschieden, wobei die histopathologische Typisierung von geringerer prognostischer Relevanz ist als der histopathologische Differenzierungsgrad und die Tumorgröße; diese beiden Prognosefaktoren sind daher in der Stadieneinteilung der UICC berücksichtigt [1, 4, 5, 6].
In diesem Kapitel werden ausschießlich Weichteilsarkome des Erwachsenen berücksichtigt. Hinsichtlich der Therapie von Ewing- und Kaposi-Sarkomen wird auf die entsprechenden Kapitel dieses Buches, hinsichtlich der Therapie von Weichteilsarkomen des Kindes- und Jugendalters auf entsprechende pädiatrische Behandlungsprotokolle verwiesen.
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Scütte, J., Stuschke, M., Seeber, S. (1995). Weichteilsarkome. In: Seeber, S., Schütte, J. (eds) Therapiekonzepte Onkologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-10494-1_35
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