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Pediatric metabolic liver diseases:Evolving role of liver transplantation 被引量:1

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摘要 Metabolic liver diseases(MLD)are the second most common indication for liver transplantation(LT)in children.This is based on the fact that the majority of enzymes involved in various metabolic pathways are present within the liver and LT can cure or at least control the disease manifestation.LT is also performed in metabolic disorders for end-stage liver disease,its sequelae including hepatocellular cancer.It is also performed for preventing metabolic crisis’,arresting progression of neurological dysfunction with a potential to reverse symptoms in some cases and for preventing damage to end organs like kidneys as in the case of primary hyperoxalosis and methyl malonic acidemia.Pathological findings in explant liver with patients with metabolic disease include unremarkable liver to steatosis,cholestasis,inflammation,variable amount of fibrosis,and cirrhosis.The outcome of LT in metabolic disorders is excellent except for patients with mitochondrial disorders where significant extrahepatic involvement leads to poor outcomes and hence considered a contraindication for LT.A major advantage of LT is that in the post-operative period most patients can discontinue the special formula which they were having prior to the transplant and this increases their well-being and improves growth parameters.Auxiliary partial orthotopic LT has been described for patients with noncirrhotic MLD where a segmental graft is implanted in an orthotopic position after partial resection of the native liver.The retained native liver can be the potential target for future gene therapy when it becomes a clinical reality.
出处 《World Journal of Transplantation》 2021年第6期161-179,共19页 世界移植杂志
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  • 1Urata K,Kawasaki S,Matsunami H,et al.Calculation of child and adult standard liver volume for liver transplantation. Hepatology . 1995
  • 2Bosma PJ,Chowdhury JR,Bakker C,et al.The genetic basis of the reduced expression of bilirubin UDP-glucu-ronosyltransferase 1 in Gilbert’s syndrome. The New England Journal of Medicine . 1995
  • 3Schauer R,Stangl M,Lang T, et al.Treatment of Crigler-Najjar type 1 disease: relevance of early liver transplantation. Journal of Pediatric Surgery . 2003
  • 4Oakden W K,Moore A M,Blaser S,et al.HMR spec-troscopic characteristics of kernicterus:apossible meta-bolic signature. American Journal of Neuroradiology . 2005
  • 5Katar S,Akay HO,Taskesen M.Clinical and cranial magnetic resonance imaging(MRI ) findings of 21 patients with serious hyperbilirubinemia. Journal of Child Neurology . 2008
  • 6Ozcay F,Alehan F,Sevmis S, et al.Living related liver transplantation in Crigler-Najjar syndrome type 1. Transplantation Proceedings . 2009
  • 7Yohannan MD,Terry HJ,Littlewood JM.Long term phototherapy in Crigler-Najjar syndrome. Archives of Disease in Childhood . 1983
  • 8Sugama S,Soeda A,Eto Y.Magnetic resonance imaging in three children with kernicterus. Pediatric Neurology . 2001
  • 9Rela,M,Muiesan,P,Vilca-Melendez,H,Dhawan,A.Auxiliary partial orthotopic liver transplantation for Crigler-Najjar syndrome type I. Annals of Surgery . 1999
  • 10van der Veere CN,Sinaasappel M,McDonagh AF,Rosenthal P,Labrune P,Odievre M, et al.Current therapy for Crigler- Najjar syndrome type 1: report of a world registry. Hepatology . 1996

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