Zusammenfassung
Das Chemotherapie-assoziierte hämolytisch-urämische Syndrom (c-HUS) gehört zum Formenkreis der thrombotischen Mikroangiopathien, die sich durch systemische oder renale Thrombozytenaggregation, Thrombozytopenie, mechanische Schädigung der Erythrozyten mit hämolytischer Anämie und mögliche Endorganschädigung durch Okklusionen kleiner Gefäße auszeichnen. Dem c-HUS liegt eine primäre Endothelschädigung zugrunde, was zu einem Verlust der antithrombogenen Charakteristika des Endothels führt, gefolgt von einer Freisetzung von ultralangen Multimeren des von-Willebrand-Faktors, Gefäßwandverdickung und intraluminalen Thrombozytenthromben. Typische Onkologika als Auslöser eines c-HUS sind Mitomycin C, Gemcitabine, Cisplatin sowie gegen VEGF gerichtete monoklonale Antikörper oder orale Tyrosinkinaseinhibitoren. Obwohl es sich beim c-HUS um eine sehr seltene unerwünschte Arzneimittelwirkung handelt, sollte der behandelnde Onkologe auf Zeichen eines möglichen c-HUS achten. Die Behandlung umfasst den sofortigen Therapiestopp, eine antihypertensiven Behandlung, Plasmaaustausch oder Dialyse falls indiziert. Die zusätzliche Gabe von Steroiden oder Thrombozytenaggregationshemmern bringt keinen klinischen Nutzen.
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Joerger, M., Cerny, T. (2020). Tumorassoziiertes hämolytisch-urämisches Syndrom (c-HUS) durch antineoplastische Substanzen. In: Schmoll, HJ. (eds) Kompendium Internistische Onkologie . Springer Reference Medizin. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-46764-0_288-1
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