Acquired hemophilia A and von Willebrand syndrome in a patient with late-onset systemic lupus erythematosus

Acquired hemophilia A (AHA) and acquired von Willebrand Syndrome (AVWS) are both rare bleeding disorders that can be associated with lymphoproliferative or autoimmune diseases. AHA is uniformly caused by inhibitory autoantibodies against coagulation factor VIII (FVIII), while the pathophysiology of...

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Autors principals: Dicke, Christina, Holstein, Katharina, Schneppenheim, Sonja, Dittmer, Rita, Schneppenheim, Reinhard, Bokemeyer, Carsten, Iking-Konert, Christof, Budde, Ulrich, Langer, Florian
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2014
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4147383/
https://ncbi.nlm.nih.gov/pubmed/25170428
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2162-3619-3-21
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