Treatment of Acquired von Willebrand Syndrome with Intravenous Immunoglobulin

Yale S Arkel; Jean Lynch; Mikio Kamiyama

doi:10.1055/s-0038-1648928

Thrombosis and Haemostasis, Inhaltsverzeichnis

Thromb Haemost 1994; 72(04): 643-644
DOI: 10.1055/s-0038-1648928

Letter to the Editor

Schattauer GmbH Stuttgart

Treatment of Acquired von Willebrand Syndrome with Intravenous Immunoglobulin

Autor*innen

Yale S Arkel

The Blood Disorder Center, Overlook Hospital, Summit, NJ, USA
Jean Lynch

The Blood Disorder Center, Overlook Hospital, Summit, NJ, USA
Mikio Kamiyama

The Blood Disorder Center, Overlook Hospital, Summit, NJ, USA

Abstract

als PDF herunterladen

PDF (136 kb)

Referenzen

References
1 Mannucci PM, Lombardi R, Bader R, Horellou MH, Finazzi G, Besana C, Conard J, Samama M. Studies of the pathophysiology of acquired von Willebrand’s Disease in seven patients with lymphoproliferative disorders or benign monoclonal gammopathies. Blood 1984; 64: 614-621
2 Handin RI, Martin V, Moloney WC. Antibody-induced von Willebrand,s disease: A newly defined inhibitor syndrome. Blood 1976; 48: 393-405
3 Simone JV, Cornet JA, Abildgaard CF. Acquired von Willebrand,s syndrome in systemic lupus erythematosus. Blood 1968; 31: 806-812
4 Joist JH, Cowan JF, Zimmerman TS. Acquired von Willebrand,s disease, evidence for a quantitative and qualitative factor VIII deficiency. New Eng J Med 1978; 298: 988-991
5 McGrath KM, Johnson CA, Stuart JJ. Acquired von Willebrand,s disease associated with an inhibitor to Factor VIII antigen and gastrointestinal telangiectasia. Am J Med 1979; 67: 693-696
6 Meyer D, Frommel D, Larrieu MJ, Zimmerman TS. Selective absence of large forms of factor VUI/von Willebrand factor in acquired von Willebrand,s syndrome. Response to transfusion. Blood 1970; 54: 600-606
7 Sampson BM, Greaves M, Malia RG, Preston FE. Acquired von Willebrand,s disease: Demonstration of a circulating inhibitor to the factor VIII complex in four cases. Br J Haematol 1983; 54: 233-244
8 Stableforth P, Tamagnini GL, Dormandy KM. Acquired von Willebrand,s syndrome with inhibitors both to factor VIII clotting activity and ristocetin-induced platelet aggregation. Br J Haematol 1976; 33: 565-573
9 Hanley D, Arkel YS, Lynch J, Kamiyama M. Acquired von Willebrand,s Syndrome in Association with a Lupus-Like Anticoagulant Corrected by Intravenous Immunoglobulin. Am J Hematol 1994; 46: 141-146
10 Delmer A, Horellou MH, Brechot JM, Prudent J, Potevin F, Lecrubier C, Girard-Longhini C, Samama M, Zittoun R. Acquired von Willebrand,s disease: Correction of hemostatic defect by high-dose intravenous immunoglobulins. Am J Hematol 1992; 40: 151-152
11 White LA, Chisholm M. Gastro-intestinal bleeding in acquired von Willebrand,s disease: efficacy of high-dose immuno-globulin where substitution treatment failed. Br J Haematol 1993; 84: 332-334