Literature DB >> 6403924

[Antifactor VIII antibody in Rosai-Dorfman disease].

J L Lorenzini, J P Allain, J M Chalopin, G Rifle, E Devilliers, P M Carli, P Cortet, J Bonhomme.   

Abstract

The case of a 72 year-old man with a sinus histiocytosis is reported. The clinical course was characterised by an hemorrhagic disorder linked to a factor VIII inhibitor. The characteristics of the antibody titer, affinity and saturability have been studied. In an attempt to stop the bleeding treatment included human and porcine factor VIII concentrates, plasmapheresis and immunosuppressive drugs. Repeated plasma exchanges did not modify the inhibitor titer for more than 24 h.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6403924

Source DB:  PubMed          Journal:  Nouv Rev Fr Hematol


  1 in total

1.  Haemophilia due to factor VIII inhibitors in a patient suffering from an autoimmune disease: treatment with intravenous immunoglobulin. A case report.

Authors:  A Gianella-Borradori; A Hirt; A Lüthy; H P Wagner; P Imbach
Journal:  Blut       Date:  1984-06
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.