Zusammenfassung
Mit ein bis zwei Erkrankungen pro 1.000.000 Personen pro Jahr handelt es sich bei den Neoplasien des Magens um eine sehr seltene Tumorentität. Bezogen auf alle gastrointestinalen neuroendokrinen Neoplasien (gen) sind circa 9 % primär gastrale Neoplasien. Hauptlokalisation sind Magenfundus und -korpus. Die neuroendokrinen Neoplasien des Magens sind in drei bzw. vier Subtypen unterteilt. Das therapeutische Vorgehen hängt neben dem Subtyp der gastralen neuroendokrinen Neoplasie von Funktionalität, Differenzierungsgrad, Stadium, ECOG-Performance-Status und nicht zuletzt der Komorbidität des Patienten ab. Prognostisch bestehen erhebliche Unterschiede zwischen den Genen-Subtypen.
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Luley, K. (2023). Neuroendokrine Neoplasien des Magens. In: Lehnert, H., Märker-Hermann, E., Marx, N., Meyhöfer, S.M. (eds) DGIM Innere Medizin. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-54676-1_509-2
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DOI: https://doi.org/10.1007/978-3-642-54676-1_509-2
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Neuroendokrine Neoplasien des Magens- Published:
- 27 August 2023
DOI: https://doi.org/10.1007/978-3-642-54676-1_509-2
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Neuroendokrine Neoplasien des Magens- Published:
- 13 October 2015
DOI: https://doi.org/10.1007/978-3-642-54676-1_509-1