Living donor liver transplantation in Budd-Chiari syndrome: a single-center experience

G S Choi1, J B Park, G O Jung

  • 1Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Insights

Living donor liver transplantation (LDLT) is a viable option for Budd-Chiari syndrome (BCS) patients. Surgical modifications enable successful LDLT for BCS, achieving excellent patient and graft survival rates.

Area of Science:

  • Hepatology
  • Transplantation Surgery
  • Vascular Surgery

Background:

  • Budd-Chiari syndrome (BCS) involves hepatic venous outflow obstruction, often treated with caval resection, precluding liver transplantation.
  • Living donor liver transplantation (LDLT) presents unique challenges for BCS patients due to potential caval involvement.

Purpose of the Study:

  • To evaluate the safety and efficacy of LDLT in BCS patients.
  • To describe surgical modifications for LDLT in BCS, addressing hepatic venous and inferior vena cava (IVC) obstruction.

Main Methods:

  • Retrospective analysis of 4 BCS patients undergoing LDLT between January 2003 and December 2007.
  • Surgical techniques included RHV resection with IVC anastomosis, retrohepatic IVC reconstruction, and mesoatrial shunt conversion.

Main Results:

  • All 4 patients successfully underwent LDLT for BCS.
  • 100% patient and graft survival rates were observed.
  • Minimal complications occurred in donors and recipients.

Conclusions:

  • LDLT is a safe and effective treatment for BCS when employing appropriate venous drainage techniques.
  • Anticoagulant therapy and diligent follow-up are crucial for managing BCS post-LDLT and preventing recurrence.