Acquired factor V inhibitor: aetiology, bleeding risk and treatment with regard to three cases.

Citation
N. Schleinitz et al., Acquired factor V inhibitor: aetiology, bleeding risk and treatment with regard to three cases., REV MED IN, 22(11), 2001, pp. 1119-1123
Citations number
23
Categorie Soggetti
General & Internal Medicine
Journal title
REVUE DE MEDECINE INTERNE
ISSN journal
02488663 → ACNP
Volume
22
Issue
11
Year of publication
2001
Pages
1119 - 1123
Database
ISI
SICI code
0248-8663(200111)22:11<1119:AFVIAB>2.0.ZU;2-H
Abstract
Introduction. - Acquired factor V inhibitor is rare and clinical symptoms a re quite variable. Bleeding is the leading symptom but some patients are as ymptomatic. Several diseases or conditions are associated with factor V inh ibitors. Various treatments have been attempted but randomized or prospecti ve trials are not available. Exegesis. - Here we report three cases of acquired factor V inhibitor These reports highlight the clinical variability of this disorder. Pathogenesis and therapy with reference to the literature are discussed. Conclusion. - Factor V inhibitors are rare and associated to several diseas es or conditions. Pathogenesis is still unclear except in patients exposed to bovine thrombin. The majority of the cases developed after surgery. In a few cases there is an association to a malignant or autoimmune disease. Pl asmapheresis and platelet transfusions might be the best treatment in case of severe bleeding. High-dose intravenous immunoglobulin infusions have bee n used successfully in some cases and we report here their efficacy in two cases. (C) 2001 Editions scientifiques et medicales Elsevier SAS.