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Extractions: Z USAMMENFASSUNG Hintergrund: Klinisches Bild: Eine ausgeprägte Thrombophilie, rezidivierende Fehlgeburten sowie eine Thrombozytopenie charakterisieren die klinische Trias des Antiphospholipidsyndroms. Andere klinische Manifestationen umfassen: Migräne, Chorea minor, hämolytische Anämie, Erkrankungen der Herzklappen, Budd-Chiari-Syndrom, rezidivierende Pankreatitiden, intestinale Apoplexie, maligne Hypertonie, Livedo reticularis, Präeklampsie, fetale Wachstumsverzögerungen oder das sogenannte katastrophale Antiphospholipidantikörpersyndrom". Im Gegensatz zum primären Antiphospholipidantikörpersyndrom" finden sich Lupusantikoagulanzien und Anticardiolipinantikörper beim sekundären Antiphospholipidantikörpersyndrom" im Rahmen von Autoimmunerkrankungen, von Neoplasien und Infektionen oder sind mit dem Gebrauch bestimmter Medikamente assoziiert. Therapie:
