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Neuroendokrine Neoplasien des Magens

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DGIM Innere Medizin

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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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Correspondence to Kim Luley .

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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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Chapter history

  1. Latest

    Neuroendokrine Neoplasien des Magens
    Published:
    27 August 2023

    DOI: https://doi.org/10.1007/978-3-642-54676-1_509-2

  2. Original

    Neuroendokrine Neoplasien des Magens
    Published:
    13 October 2015

    DOI: https://doi.org/10.1007/978-3-642-54676-1_509-1