[Budd-Chiari syndrome--a rare manifestation of hereditary thrombophilia]

Chirurg. 2000 Apr;71(4):462-5. doi: 10.1007/s001040051084.
[Article in German]

Abstract

Budd-Chiari syndrome is a rare manifestation of hereditary or acquired thrombophilia. We saw a case of Budd-Chiari syndrome in a 30-year-old woman leading to initial diagnostic difficulties. She underwent surgical side-to-side shunt and 9 weeks later an almost normal liver could be demonstrated on computerized tomography. Budd-Chiari syndrome should be considered if the Chiari triad with abdominal pain, hepatomegaly and ascites occurs in a patient. If necessary, invasive diagnostic procedures (e.g. angiography) must be performed. Therapeutic options are anticoagulative therapy and porto-systemic shunt, either as a TIPS or a surgical shunt. If severe liver failure occurs or liver cirrhosis is present, orthotopic liver transplantation is an additional option which also cures hereditary thrombophilia.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Activated Protein C Resistance / diagnosis
  • Activated Protein C Resistance / genetics*
  • Activated Protein C Resistance / surgery
  • Adult
  • Budd-Chiari Syndrome / diagnosis
  • Budd-Chiari Syndrome / genetics*
  • Budd-Chiari Syndrome / surgery
  • Diagnosis, Differential
  • Factor V / genetics*
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Portasystemic Shunt, Surgical
  • Thrombophilia / diagnosis
  • Thrombophilia / genetics*
  • Thrombophilia / surgery

Substances

  • factor V Leiden
  • Factor V