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Myelodysplastische Syndrome

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Geriatrische Onkologie

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Zusammenfassung

Die Myelodysplastischen Syndrome (MDS) sind eine heterogene Gruppe erworbener klonaler Erkrankungen des Knochenmarks. Sie sind mit einem medianen Manifestationsalter zwischen 70 und 80 Jahren vorwiegend eine Erkrankung des älteren Menschen. Ein MDS tritt zumeist primär ohne erkennbaren Grund oder in Folge einer Exposition gegenüber Chemotherapeutika, Strahlen oder anderen Noxen (z. B. Benzol) auf. Klinisch manifestiert sich das MDS durch ein fortschreitendes Knochenmarkversagen bei ineffektiver Hämatopoese mit peripherer Zytopenie und einem Risiko für eine Transformation in eine akute myeloische Leukämie (AML). Die Prognose und das Risiko für eine Transformation in eine AML werden vor allem durch den Blastenanteil und molekulargenetische bzw. zytogenetische Aberrationen bestimmt. Die therapeutischen Strategien umfassen reine Supportivmaßnahmen, Therapien mit immunmodulatorischen Substanzen, demethylierende Substanzen sowie die allogene Stammzelltransplantation als einzige kurative Therapie.

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Correspondence to Franziska La Meir .

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La Meir, F., Boch, T., Nowak, D., Metzgeroth, G., Hofmann, WK. (2018). Myelodysplastische Syndrome. In: Ebert, M., Härtel, N., Wedding, U. (eds) Geriatrische Onkologie. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-48727-3_14

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  • DOI: https://doi.org/10.1007/978-3-662-48727-3_14

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