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

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 skin eryt...

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Enregistré dans:
Détails bibliographiques
Publié dans:Res Pract Thromb Haemost
Auteurs principaux: Beckmann, Lennart, Voigtlaender, Minna, Holstein, Katharina, Lennartz, Maximilian, Schneider, Stefan W., Haddad, Munif, Renné, Thomas, Bokemeyer, Carsten, Rolling, Christina C., Langer, Florian
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2021
Sujets:
Case Report
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC8265818/
https://ncbi.nlm.nih.gov/pubmed/34263105
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/rth2.12559
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