{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,1]],"date-time":"2025-11-01T12:54:55Z","timestamp":1762001695065},"reference-count":30,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2012,2,24]],"date-time":"2012-02-24T00:00:00Z","timestamp":1330041600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatric Transplantation"],"published-print":{"date-parts":[[2012,3]]},"abstract":"<jats:p>Ko JS, Yi N\u2010J, Suh KS, Seo JK. Pediatric liver transplantation for fibropolycystic liver disease. Pediatr Transplantation 2012: 16: 195\u2013200. \u00a9 2012 John Wiley &amp; Sons A\/S.<\/jats:p><jats:p><jats:bold>Abstract:\u2002<\/jats:bold> Fibropolycystic liver disease includes CHF, Caroli\u2019s syndrome, and Caroli\u2019s disease. Patients with Caroli\u2019s disease and Caroli\u2019s syndrome have an increased risk of recurrent cholangitis, intrahepatic calculi, biliary cirrhosis, and cholangiocarcinoma. The aim of this study was to examine the post\u2010transplantation outcomes of children with fibropolycystic liver disease. Of the 158 children transplanted at Seoul National University Hospital, there were four patients with Caroli\u2019s syndrome, two patients with CHF, and one patient with Caroli\u2019s disease. One patient underwent combined liver\/kidney transplantation. Associated renal manifestations included ARPKD in three children and nephronophthisis in one child. The indications for LT were recurrent cholangitis, decompensated cirrhosis, and refractory complications of portal hypertension. Both graft and patient survival rates were 100% at a median follow\u2010up period of two\u2003yr after LT. Three children with growth failure achieved catch\u2010up growth after LT. In three patients with ARPKD, mean serum creatinine levels increased from 0.53\u2003mg\/dL at the time of LT to 0.91\u2003mg\/dL at the last follow\u2010up (p<jats:italic>\u2003<\/jats:italic>=<jats:italic>\u2003<\/jats:italic>0.01). LT is an excellent option for children with complications from fibropolycystic liver disease. Renal function should be monitored cautiously after LT in the patients with ARPKD.<\/jats:p>","DOI":"10.1111\/j.1399-3046.2012.01661.x","type":"journal-article","created":{"date-parts":[[2012,2,24]],"date-time":"2012-02-24T07:14:44Z","timestamp":1330067684000},"page":"195-200","source":"Crossref","is-referenced-by-count":27,"title":["Pediatric liver transplantation for fibropolycystic liver disease"],"prefix":"10.1111","volume":"16","author":[{"given":"Jae Sung","family":"Ko","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nam\u2010Joon","family":"Yi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kyung Suk","family":"Suh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jeong 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