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- Title
PUBLICATION ONLY ABSTRACTS.
- Abstract
B Disclosure of Interest b : None declared PU07 ACQUIRED VON WILLEBRAND SYNDROME J. Cabral SP 1,* sp ; M. Calheiros SP 1 sp ; C. Calaza SP 1 sp ; A. Marques SP 1 sp SP 1 sp I Immunohemotherapy Service, Hospital de Braga, Braga, Portugal i B Introduction b : The acquired von Willebrand syndrome (AvWS) is a rare bleeding disorder with laboratory findings similar to those of inherited vWD, however, AvWS occurs in patients with negative personal and family history of bleeding. After the chemotherapy treatment, complete remission of the lymphoma was observed, accompanied by normal haemostasis with no new episodes of haemorrhagic diathesis after more than one year of follow-up. B Discussion/Conclusion b : A prolonged aPTT could be indicative of avWD especially in patients with other underlying haematological disease. Service offerd by center is clinical, laboratory,counselling,therapeutic and physiotherapy and all specialist service available as center situated at government hospital, Surat Total number of hemophilia A patient- 575 Total number of hemophilia B patient - 75 Out of this patient total number of inhibitor patient 50 in our hemophilia care center. A. Amireche SP 1,* sp ; A. Kessira SP 1 sp ; H. Brouk SP 1 sp SP 1 sp I Hemobiology and blood transfusion center, Faculty of medicine, University Badji Mokhtar of Annaba, Annaba, Algeria i B Introduction b : Acquired hemophilia A (AHA) is a rare hemorrhagic disease secondary to the development of an autoantibody to factor VIII.
- Subjects
VON Willebrand disease; AVULSION fractures; HEALTH facilities; BLOOD coagulation disorders; CIRCULATING anticoagulants
- Publication
Haemophilia, 2023, Vol 29, p203
- ISSN
1351-8216
- Publication type
Article
- DOI
10.1111/hae.14716