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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Detalles Bibliográficos
Autores principales: Beckmann, Lennart, Voigtlaender, Minna, Holstein, Katharina, Lennartz, Maximilian, Schneider, Stefan W., Haddad, Munif, Renné, Thomas, Bokemeyer, Carsten, Rolling, Christina C., Langer, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265818/
https://www.ncbi.nlm.nih.gov/pubmed/34263105
http://dx.doi.org/10.1002/rth2.12559

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265818/
https://www.ncbi.nlm.nih.gov/pubmed/34263105
http://dx.doi.org/10.1002/rth2.12559

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