Monocyte activation and acquired autoimmune protein S deficiency promote disseminated intravascular coagulation in a patient with primary antiphospholipid syndrome

Abstract Autoimmune protein S (PS) deficiency is a highly thrombotic, potentially life‐threatening disorder. Its pathophysiological relevance in the context of primary antiphospholipid syndrome (APS) is unclear. Here, we report the case of a 76‐year‐old woman, who presented with a painful reticular...

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Váldodahkkit:	Lennart Beckmann, Minna Voigtlaender, Katharina Holstein, Maximilian Lennartz, Stefan W. Schneider, Munif Haddad, Thomas Renné, Carsten Bokemeyer, Christina C. Rolling, Florian Langer
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Elsevier 2021-07-01
Ráidu:	Research and Practice in Thrombosis and Haemostasis
Fáttát:	antiphospholipid syndrome disseminated intravascular coagulation monocytes protein S tissue factor
Liŋkkat:	https://doi.org/10.1002/rth2.12559
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