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Tumorassoziierte Genodermatosen

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Braun-Falco's Dermatologie, Venerologie und Allergologie

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Zusammenfassung

Die tumorassoziierten Genodermatosen sind extrem seltene autosomal-dominant erbliche Erkrankungen, die durch typische Hauterscheinungen charakterisiert sind und zur Entstehung maligner Tumoren verschiedener Organe disponieren. Die diagnostische Einordnung der häufig vorangehenden Hauterscheinungen ermöglicht daher die Identifizierung von Patienten mit einem angeborenen Risiko für die Entwicklung spezifischer Krebserkrankungen und liefert somit einen wichtigen Beitrag zur Krebsprävention.

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Author information

Authors and Affiliations

  1. Klinik und Poliklinik für Dermatologie, Universitätsklinikum Regensburg, Regensburg, Deutschland

    Mark Berneburg

  2. Gemeinschaftspraxis für Dermatologie, Paderborn, Deutschland

    Roland Kruse

Authors
  1. Mark Berneburg
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  2. Roland Kruse
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Corresponding author

Correspondence to Mark Berneburg .

Editor information

Editors and Affiliations

  1. Dermatologie und Allergologie, Universitätsklinikum München Klinik und Poliklinik für, München, Bayern, Germany

    Gerd Plewig

  2. Dermatologie und Allergologie, Universitätsklinikum München Klinik und Poliklinik für, München, Bayern, Germany

    Thomas Ruzicka

  3. J.W.Goethe-Universität, Klinik für Dermatologie, Venerologie und Allergologie, Frankfurt, Hessen, Germany

    Roland Kaufmann

  4. Univ.Klinikum Marburg Klinik für Dermatologie und Allergologie, Marburg, Germany

    Michael Hertl

Section Editor information

  1. Direktor der Klinik für Dermatologie, Venerologie und Allergologie, Klinikum der J.W.Goethe-Universität, Frankfurt am Main, Deutschland

    Roland Kaufmann

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Berneburg, M., Kruse, R. (2018). Tumorassoziierte Genodermatosen. In: Plewig, G., Ruzicka, T., Kaufmann, R., Hertl, M. (eds) Braun-Falco's Dermatologie, Venerologie und Allergologie. Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-49546-9_114-1

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  • DOI: https://doi.org/10.1007/978-3-662-49546-9_114-1

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  • Print ISBN: 978-3-662-49546-9

  • Online ISBN: 978-3-662-49546-9

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