Zusammenfassung
Die autoimmunhämolytischen Anämien sind bei Kindern selten. Wenn sie auftreten, sind sie meistens durch eine akute und schwere Hämolyse gekennzeichnet. Wichtigster diagnostischer Test ist neben dem Blutbild der positive direkte Coombs-Test. Nach dem Reaktionsoptimum der Autoantikörper unterscheidet man Wärmeautoantikörper und Kälteautoantikörper. In der Regel sind die autoimmunhämolytischen Anämien sekundäre Erkrankungen, so dass nach primären Grunderkrankungen, besonders solchen aus dem Formenkreis der Autoimmunerkrankungen und nach Immundefekten, gesucht werden muß. Auch im Rahmen von Infektionen können sie auftreten. Medikamentös induzierte Formen sind bei Kindern selten. Für eine adäquate Behandlung ist eine enge Zusammenarbeit zwischen Klinik und Transfusionsmedizin erforderlich, zumal sich die Transfusionstherapie, vor allem im Initialstadium, schwierig gestalten kann.
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Salama, A., Gaedicke, G. (2006). Autoimmunhämolytische Anämien. In: Gadner, H., Gaedicke, G., Niemeyer, C., Ritter, J. (eds) Pädiatrische Hämatologie und Onkologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-29036-2_11
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DOI: https://doi.org/10.1007/3-540-29036-2_11
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