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Erschienen in: Herz 4/2017

27.04.2017 | CME

Inflammatorische Kardiomyopathie und Myokarditis

verfasst von: Prof. Dr. B. Maisch, Prof. A. D. Ristic, Prof. Dr. S. Pankuweit

Erschienen in: Herz | Ausgabe 4/2017

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Zusammenfassung

In diesem Beitrag werden Diagnostik, Differenzialdiagnostik, multimodale Bildgebung sowie medikamentöse und invasiv diagnostische Therapie der inflammatorischen Kardiomyopathie und Myokarditis unter ätiologischen Gesichtspunkten und in Anlehnung und Fortentwicklung des Positionspapiers der Working Group Myocardial and Pericardial Disease der European Society of Cardiology beschrieben. Im Vordergrund der Diagnostik steht die ätiopathogenetische Einordnung der inflammatorischen Kardiomyopathie, die klinisches Bild, Verlauf, Therapie und Prognose prägen. Die virale Myokarditis wird von der sterilen autoreaktiven (autoimmunen) Form durch histologische und molekulare Untersuchungen in der Myokardbiopsie abgegrenzt. Dies führt zu einer individualisierten, ätiologisch fundierten und gezielten Behandlung jenseits einer reinen Herzinsuffizienzbehandlung.
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Metadaten
Titel
Inflammatorische Kardiomyopathie und Myokarditis
verfasst von
Prof. Dr. B. Maisch
Prof. A. D. Ristic
Prof. Dr. S. Pankuweit
Publikationsdatum
27.04.2017
Verlag
Springer Medizin
Erschienen in
Herz / Ausgabe 4/2017
Print ISSN: 0340-9937
Elektronische ISSN: 1615-6692
DOI
https://doi.org/10.1007/s00059-017-4569-y

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