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Myositiden als Leitsymptom maligner Tumoren. Diagnostische und pathogenetische Aspekte

  • Conference paper
Hämoblastosen Zentrale Motorik Iatrogene Schäden Myositiden

Part of the book series: Verhandlungen der Deutschen Gesellschaft für Neurologie ((VDGNEUROLOGIE,volume 2))

Zusammenfassung

Das Syndrom der Dermato-Polymyositiden (DPM) ist so häufig mit malignen Tumoren kombiniert, daß in jedem einzelnen Fall eine genaue und nötigenfalls wiederholte Suche nach einem Malignom durchgeführt werden muß. Sie wird zwischen 3 % (42) und 26 % (30) der Patienten erfolgreich sein, im Mittel in 12 % (unter 2520 DPM-Fallen aus 30 Literaturstellen findet sich 294mal die Kombination mit einem Tumor (56)). Die Angaben schwanken, je nachdem ob allein die Polymyositis (PM), die Dermatomyo-sitis (DM) oder beide zusammen betrachtet wurden, je nach Größe des Kollektivs, nach Alters- und Geschlechtsverteilung und mit dem Spektrum der jeweils möglichen Untersuchungen.

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Authors
  1. K. Schimrigk
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  2. J. Steffen
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Editor information

Editors and Affiliations

  1. Neurologische Abteilung, Allgemeinen Krankenhauses St. Georg, Lohmühlenstr. 5, D-2000, Hamburg 1, Deutschland

    Dieter Seitz

  2. Neurologische Universitätsklinik, Sigmund-Freud-Str. 25, D-5300, Bonn-Venusberg, Deutschland

    Peter Vogel

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© 1983 Springer-Verlag Berlin Heidelberg

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Schimrigk, K., Steffen, J. (1983). Myositiden als Leitsymptom maligner Tumoren. Diagnostische und pathogenetische Aspekte. In: Seitz, D., Vogel, P. (eds) Hämoblastosen Zentrale Motorik Iatrogene Schäden Myositiden. Verhandlungen der Deutschen Gesellschaft für Neurologie, vol 2. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-45561-2_32

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  • DOI: https://doi.org/10.1007/978-3-642-45561-2_32

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-12341-5

  • Online ISBN: 978-3-642-45561-2

  • eBook Packages: Springer Book Archive

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