Resumen. DIAZ CONCEPCION, Alina. Acquired von Willebrand’s disease. General aspects. Rev Cubana Hematol Inmunol Hemoter [online]. , vol, n La hemofilia A adquirida (HAA) es un trastorno hemorrágico poco frecuente entre otros, enfermedades autoinmunes y malignas y durante el embarazo, parto y .. of the management of acquired haemophilia and von Willebrand syndrome. enfermedad von willebrand adquirida pdf. Quote. Postby Just» Tue Aug 28, am. Looking for enfermedad von willebrand adquirida pdf. Will be.
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Successful use of mycophenolate mofetil and prednisone in willebran 14 year-old girl with acquired hemophilia A. Summary Acquired Von Willebrand disease is an unusual situation arising within the context of self-immune diseases, lymphoproliferative and mieloproliferative disorders. Thromb Diath Haemorr ; Mudad R, Kane WH.
A description of three cases and literature review. The use of recombinant factor VIIa in the treatment of bleeding disorders.
Experience of two Italian Centres wilebrand 17 new cases. Case report and review of the literature. Clin Appl Thromb Hemost ;6: Tolerability and safety of Rituximab Mabthera. A longitudinal analysis of 24 patients.
What is the abbreviation for enfermedad de von Willebrand adquirida?
Los productos que sortean el efecto del inhibidor: Bulevar Artigas CP The management of acquired haemophilia. A review of the literature with special reference to the value of steroid and immunosuppresive treatment.
All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Chemotherapy with thalidomide, cyclophosphamide and dexamethasone was indicated for the base disease and there was favourable evolution, the hemorrhagic syndrome remitted and there was a tendency to crasis normalization, the same as globular and platelets values ongoing normalization after six series of treatment.
Acquired disorders of coagulation. Basic Principles and Clinical Practice. Br J Haematol ; Ciudad de La Habana, Cuba.
enfermedad von willebrand adquirida pdf
Hemorrhagic manifestations are variable and mainly of mucous cutaneous type. A more uniform measurement of factor VIII inihibitors.
Epidemiology and general guidelines of the management of acquired haemophilia and von Willebrand syndrome. Sibilia J, Sordet C. Am J Haematol ; Am J Hematol ; International recommendations on the diagnosis and treatment of patients with acquired hemophilia Voh.
Enfermedad de von Willebrand adquirida. Aspectos generales
Lippincott, Williams and Wilkins; Inhibitors against factor VIII in patients with cancer. Semin Thromb Hemost ; Successful treatment with Rituximab followed by sigmoidectomy. Adquiridq of acquired haemophilia with factor eight inhibitor bypassing activity.
Baillieres Clin Haematol ;9: Guidelines on the investigation and management of the anti-phospholipid syndrome.
Rituximab for autoimmune haemophilia: Abshire T, Kenet G. Postpartum acquired factor VIII inhibitors: Review and meta-analysis focused on therapy adquiridz prognostic factors. A prospective, randomized trial of prednisone and cyclophosphamide in the treatment of patients with factor VIII autoantibodies.