Recurrence of primary biliary cirrhosis and primary sclerosing cholangitis after liver transplantation in Japan

被引:19
|
作者
Yamagiwa, Satoshi
Ichida, Takafumi
机构
[1] Juntendo Univ, Sch Med, Div Gastroenterol & Hepatol, Nagaoka, Izunokuni 4102295, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Div Gastroenterol & Hepatol, Niigata, Japan
关键词
living-donor liver transplantation; primary biliary cirrhosis; primary sclerosing cholangitis; recurrence;
D O I
10.1111/j.1872-034X.2007.00250.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Although there was some initial controversy, there is now a consensus that primary biliary cirrhosis (PBC) does indeed recur in both cadaveric and living donated allografts. Recurrence rate after deceased donor liver transplantation (LT) was reported to be 10.9-23% at 5 years. In the present study, we reviewed 221 PBC patients who underwent living-donor liver transplantation (LDLT) in Japan. The 5-year overall survival rate was 79%, and the rate of recurrence based on histological findings was 10% (7/70) after a median time of 36 months. Primary immunosuppression, withdrawal of corticosteroids and human leukocyte antigen matches were not associated with the recurrence. Recurrent PBC appears to have little impact on graft function and survival, but this may become a greater problem with longer follow up. It is noteworthy that the 10-year survival of primary sclerosing cholangitis (PSC) patients who underwent LDLT wasfound to be only 39.1% in Japan, whereas that of PBC was 72.9%. Factors associated with the poor prognosis include biliary strictures, hepatobiliary and colorectal malignancies, and recurrence of PSC. In our study, we reviewed 66 patients with PSC who underwent LDLT in Japan. The 5-year survival rate was 72%, and the rate of recurrence diagnosed on histological and cholangiographic findings was 25% (11/44). Well-defined diagnostic criteria and longer studies are required to characterize the nature of recurrent PSC and its impact on graft survival in more detail.
引用
收藏
页码:S449 / S454
页数:6
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