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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Detalles Bibliográficos
Autores principales: Dicke, Christina, Holstein, Katharina, Schneppenheim, Sonja, Dittmer, Rita, Schneppenheim, Reinhard, Bokemeyer, Carsten, Iking-Konert, Christof, Budde, Ulrich, Langer, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147383/
https://www.ncbi.nlm.nih.gov/pubmed/25170428
http://dx.doi.org/10.1186/2162-3619-3-21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147383/
https://www.ncbi.nlm.nih.gov/pubmed/25170428
http://dx.doi.org/10.1186/2162-3619-3-21

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