Araştırma Makalesi

Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience

Cilt: 8 Sayı: 2 29 Haziran 2026
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Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience

Öz

Objective: Primary sclerosing cholangitis is a chronic, progressive cholestatic liver disease that frequently leads to liver transplantation. Although liver transplantation remains the only definitive treatment for advanced disease, post-transplant recurrence may adversely influence long-term outcomes. This study aimed to evaluate recurrence rates and clinical outcomes after liver transplantation in patients with primary sclerosing cholangitis. Matherial and Methods: This retrospective single-center study included thirty-seven patients who underwent liver transplantation between December 2004 and April 2025 due to primary sclerosing cholangitis. Demographic characteristics, clinical findings, surgical approaches, medical treatments, complications, recurrence patterns, and survival outcomes were evaluated using descriptive statistical methods. Results: The cohort consisted of sixteen males and twenty-one females with a mean age of 41.9 years at the time of transplantation. The mean disease duration was 6.1 years and the mean Model for End-Stage Liver Disease score was 18.4. Inflammatory bowel disease was present in 43 percent of patients, all diagnosed with ulcerative colitis. Living donor liver transplantation was performed in thirty-six patients, while one patient received a deceased donor graft. Incidental cholangiocarcinoma was identified in two explanted livers. During follow-up, disease recurrence developed in nine patients at a mean of 45.6 months, and two patients required re-transplantation. Five-year mortality was 13.5 percent, with three deaths associated with recurrence and related complications. Conclusion: Liver transplantation provides favorable long-term survival in patients with primary sclerosing cholangitis; however, recurrence remains a significant challenge. Structured long-term surveillance, optimized medical management, and multidisciplinary follow-up are essential to improve post-transplant outcomes.

Anahtar Kelimeler

Destekleyen Kurum

No supporting institution or financial support was received for this study.

Etik Beyan

The study was approved by the local ethics committee of the İstanbul Demiroğlu Bilim University, School of Medicine (Approval No: 51016662/44696, Date: 29.01.2025).

Kaynakça

  1. Broome U, Olsson R, Loof L, et al. Natural history and prognostic factors in 305 Swedish patients with primary sclerosing cholangitis. Gut. 1996;38(4):610-615.
  2. Farrant JM, Hayllar KM, Wilkinson ML, et al. Natural history and prognostic variables in primary sclerosing cholangitis. Gastroenterology. 1991;100(6):1710-1717.
  3. Wiesner RH, Grambsch PM, Dickson ER, et al. Primary sclerosing cholangitis: natural history, prognostic factors and survival analysis. Hepatology. 1989;10(4):430-436.
  4. Boonstra K, Beuers U, Ponsioen CY. Epidemiology of primary sclerosing cholangitis and primary biliary cirrhosis: a systematic review. J Hepatol. 2012;56(5):1181-1188.
  5. Singh S, Talwalkar JA. Primary sclerosing cholangitis: diagnosis, prognosis, and management. Clin Gastroenterol Hepatol. 2013;11(8):898-907.
  6. Lutz H, Trautwein C, Tischendorf JW. Primary sclerosing cholangitis: diagnosis and treatment. Dtsch Arztebl Int. 2013;110(51-52):867-874.
  7. EASL Clinical Practice Guidelines on sclerosing cholangitis. J Hepatol. 2022;77(3):761-806.
  8. Wheless WH, Russo MW. Treatment of Primary Sclerosing Cholangitis Including Transplantation. Clin Liver Dis. 2024;28(1):171-182.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Genel Cerrahi

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

29 Haziran 2026

Gönderilme Tarihi

8 Şubat 2026

Kabul Tarihi

31 Mart 2026

Yayımlandığı Sayı

Yıl 2026 Cilt: 8 Sayı: 2

Kaynak Göster

APA
Yazıcı, S. E., Atasever, A., Acar, Ş., & Yuzer, Y. (2026). Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience. Hitit Medical Journal, 8(2), 360-368. https://doi.org/10.52827/hititmedj.1884545
AMA
1.Yazıcı SE, Atasever A, Acar Ş, Yuzer Y. Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience. Hitit Medical Journal. 2026;8(2):360-368. doi:10.52827/hititmedj.1884545
Chicago
Yazıcı, Sinan Efe, Ahmet Atasever, Şencan Acar, ve Yıldıray Yuzer. 2026. “Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience”. Hitit Medical Journal 8 (2): 360-68. https://doi.org/10.52827/hititmedj.1884545.
EndNote
Yazıcı SE, Atasever A, Acar Ş, Yuzer Y (01 Haziran 2026) Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience. Hitit Medical Journal 8 2 360–368.
IEEE
[1]S. E. Yazıcı, A. Atasever, Ş. Acar, ve Y. Yuzer, “Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience”, Hitit Medical Journal, c. 8, sy 2, ss. 360–368, Haz. 2026, doi: 10.52827/hititmedj.1884545.
ISNAD
Yazıcı, Sinan Efe - Atasever, Ahmet - Acar, Şencan - Yuzer, Yıldıray. “Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience”. Hitit Medical Journal 8/2 (01 Haziran 2026): 360-368. https://doi.org/10.52827/hititmedj.1884545.
JAMA
1.Yazıcı SE, Atasever A, Acar Ş, Yuzer Y. Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience. Hitit Medical Journal. 2026;8:360–368.
MLA
Yazıcı, Sinan Efe, vd. “Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience”. Hitit Medical Journal, c. 8, sy 2, Haziran 2026, ss. 360-8, doi:10.52827/hititmedj.1884545.
Vancouver
1.Sinan Efe Yazıcı, Ahmet Atasever, Şencan Acar, Yıldıray Yuzer. Liver Transplantation for Primary Sclerosing Cholangitis: A 20-Year Single-Center Experience. Hitit Medical Journal. 01 Haziran 2026;8(2):360-8. doi:10.52827/hititmedj.1884545