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Leiomyosarkom des Magens

  • Conference paper
Maligne gastrointestinale Tumoren

Part of the book series: Angewandte Onkologie ((AONKOLOGIE))

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Zusammenfassung

Maligne mesenchymale Tumoren sind seltene gastrointestinale Raumforderungen. Etwa 1%–3,5% aller primären Malignóme des Magens stellen Leiomyosarkome dar. Ihr Altersgipfel liegt zwischen dem 54. und 64. Lebensjahr; Männer sind etwas häufiger betroffen als Frauen, wobei jedoch in anderen Arbeiten eine umgekehrte Geschlechtsprävalenz beobachtet wurde [1, 2]. Bei Patienten mit Leiomyosarkomen wurden chromosomale Abnormalitäten beobachtet [3]. Ein seltenes Syndrom mit einer deutlichen Prävalenz des weiblichen Geschlechts stellt das Carney-Syndrom [4, 5] dar, bei dem es im jungen Lebensalter zum Auftreten von Leiomyosarkomen (bzw. Leiomyoblastomen), extraadrenalen Paragangliomen und chondromatösen Hamartomen in der Lunge kommt.

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Authors
  1. J. Kettenbach
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Editors and Affiliations

  1. Chirurgischen Abteilung der Robert-Rössle-Klinik für Onkologie, Virchow-Klinikum der Humboldt-Universität, Berlin, Bundesrepublik Deutschland

    Peter M. Schlag (Direktor) (Direktor)

  2. 3. Medizinischen Abteilung mit Onkologie, Kaiser-Franz-Josef-Spital, Wein, Österreich

    Christian Dittrich (Vorstand Leiter) (Vorstand Leiter)

  3. Ludwig-Boltzmann-Instituts für Angewandte Kresbsforschung, Kaiser-Franz-Josef-Spital, Wein, Österreich

    Christian Dittrich (Vorstand Leiter) (Vorstand Leiter)

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© 1995 Springer-Verlag/Wien

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Kettenbach, J. (1995). Leiomyosarkom des Magens. In: Schlag, P.M., Dittrich, C. (eds) Maligne gastrointestinale Tumoren. Angewandte Onkologie. Springer, Vienna. https://doi.org/10.1007/978-3-7091-9417-1_7

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  • DOI: https://doi.org/10.1007/978-3-7091-9417-1_7

  • Publisher Name: Springer, Vienna

  • Print ISBN: 978-3-211-82716-1

  • Online ISBN: 978-3-7091-9417-1

  • eBook Packages: Springer Book Archive

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