| Literature DB >> 7532860 |
P J Van Genderen1, D N Papatsonis, J J Michiels, J J Wielenga, J Stibbe, F J Huikeshoven.
Abstract
Patients with acquired von Willebrand disease may present with severe bleeding, which is usually difficult to manage. Adequate haemostasis in acquired von Willebrand disease may be achieved with the infusion of factor VIII/von Willebrand factor concentrates or with the administration of desmopressin. We report a case of acquired von Willebrand disease with severe postoperative bleeding, responding poorly to classical von Willebrand factor replacement therapy but successfully treated with high-dose intravenous gammaglobulins. This new treatment mode of acquired von Willebrand disease is discussed in the light of a critical analysis of the literature.Entities:
Mesh:
Substances:
Year: 1994 PMID: 7532860 PMCID: PMC2398043 DOI: 10.1136/pgmj.70.830.916
Source DB: PubMed Journal: Postgrad Med J ISSN: 0032-5473 Impact factor: 2.401