Zusammenfassung
Es gibt bisher nur wenig gesicherte Erkenntnisse zur Ätiologie der Weichteil- und Knochensarkome. Einige genetische Syndrome gehen mit einer leicht erhöhten Inzidenz von Weichteilsarkomen einher. Dazu gehören neben der Neurofibromatosis Recklinghausen das Basalzellnävus-, Werner-, Gardner- und Li-Fraumeni-Syndrom sowie die tuberöse Sklerose und die familiäre Polyposis intestini, für die eine besondere Häufung von Desmoidtumoren nachgewiesen wurde.
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Budach, V., Schmitt, G. (1996). Bewegungs- und Stützorgane. In: Scherer, E., Sack, H. (eds) Strahlentherapie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79432-2_37
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