Fulminant Budd-Chiari syndrome associated with polycythemia rubra Vera and factor V Leiden mutation


AKYILDIZ M., Karasu Z. , Dheir H., Osmanoglu N., Akay S., Ilter T.

EUROPEAN JOURNAL OF INTERNAL MEDICINE, cilt.17, ss.66-67, 2006 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 17 Konu: 1
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1016/j.ejim.2005.08.007
  • Dergi Adı: EUROPEAN JOURNAL OF INTERNAL MEDICINE
  • Sayfa Sayıları: ss.66-67

Özet

Budd-Chiari syndrome (BCS) is a severe disorder characterized by hepatic venous outflow obstruction. Hypercoagulable states are the major etiological factors for the development of BCS and can be identified in about 75% of patients. Multiple etiological factors can be found in the same patient. Hematologic abnormalities, especially myeloproliferative disorders, are the most common causes of BCS. Furthermore, the prevalence of factor V Leiden mutation is three times greater in patients with BCS. Although the clinical course tends to be chronic, BCS may, on rare occasions, cause acute liver failure. Herein, we report a patient who had factor V Leiden mutation and polycythemia rubra vera, presented as fulminant BCS. (C) 2005 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved.