Living Donor Liver Transplantation for Pediatric Patients with Inheritable Metabolic Disorders

American Journal of Transplantation - Tập 5 Số 11 - Trang 2754-2763 - 2005
Daisuke Morioka1,2, Mureo Kasahara2, Yasutsugu Takada3, Jose Pablo Garbanzo Corrales3, Atsushi Yoshizawa2, Seisuke Sakamoto2, Kaoru Taira3, Elena Yukie Yoshitoshi3, Hiroto Egawa2, Hiroshi Shimada1, Kōichi Tanaka3
1Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine, 3-9, Fukuura, Kanazawa-ku, Yokohama, 236-0004, Japan
2Organ Transplant Unit, Kyoto University Hospital
3Department of Transplantation and Immunology, Kyoto University, Faculty of Medicine 54, Shogoin‐kawara‐cho, Sakyo‐ku, Kyoto, 606‐8507, Japan

Tóm tắt

Từ khóa


Tài liệu tham khảo

Shneider, 2002, Pediatric liver transplantation in metabolic disease: clinical decision making, Pediatr Transplant, 6, 25, 10.1034/j.1399-3046.2002.1p057.x

Burdelski, 2002, Liver transplantation in metabolic diseases: current status, Pediatr Transplant, 6, 361, 10.1034/j.1399-3046.2002.2e031.x

Asonuma, 1999, Living related liver transplantation from heterozygote genetic carriers to children with Wilson's disease, Pediatr Transplant, 3, 201, 10.1034/j.1399-3046.1999.00014.x

Morioka D, Takada Y, Kasahara M et al. Living donor liver transplantation for non-cirrhotic inheritable metabolic liver diseases: impact of the use of heterozygous donors. Transplantation 2005 (in press).

Kasahara, 1998, Treatment of ornithine transcarbamylase deficiency in girls by auxiliary liver transplantation: conceptual changes in living‐donor program, J Pediatr Surg, 33, 1753, 10.1016/S0022-3468(98)90278-0

Yorifuji, 2000, Living‐related liver transplantation for neonatal‐onset propionic acidemia, J Pediatr, 137, 572, 10.1067/mpd.2000.108391

Kasahara, 2004, Functional portal flow competition after auxiliary partial orthotopic living donor liver transplantation in noncirrhotic metabolic liver disease, J Pediatr Surg, 39, 1138, 10.1016/j.jpedsurg.2004.03.079

Whitington, 1998, Liver transplantation for the treatment of urea cycle disorders, J Inherit Metab Dis, 21, S112, 10.1023/A:1005317909946

Russo, 2001, Tyrosinemia: a review, Pediatr Dev Pathol, 4, 212, 10.1007/s100240010146

Matern, 1999, Liver transplantation for glycogen storage disease types I, III and IV, Eur J Pediatr, 158, S43, 10.1007/PL00014320

Bove, 2004, Bile acid synthetic defects and liver disease: a comprehensive review, Pediatr Dev Pathol, 7, 315, 10.1007/s10024-002-1201-8

Do, 2002, Benefits of chronic plasmapheresis and intravenous heme‐albumin in erythropoietic protoporphyria after orthotopic liver transplantation, Transplantation, 73, 469, 10.1097/00007890-200202150-00024

Morimoto, 1996, Guidelines for donor selection and an overview of the donor operation in living related liver transplantation, Transpl Int, 9, 208, 10.1111/j.1432-2277.1996.tb00881.x

Fujita, 2000, Hepatic grafts from live donors: donor morbidities for 470 cases of liver donation, Transpl Int, 13, 333, 10.1111/j.1432-2277.2000.tb01006.x

Hauser, 1990, Allopurinol‐induced orotiduria. A test for mutaions at the ornithine carbamoyltransferase locus in women, N Eng J Med, 322, 1641, 10.1056/NEJM199006073222305

Arranz, 1999, Optimization of allopurinol challenge: sample purification, protein intake control and the use of orotidine response as a discriminative variable improve performance of the test for diagnosing ornithine carbamoyltransferase deficiency, Clin Chem, 45, 995, 10.1093/clinchem/45.7.995

Yorifuji, 1998, X‐inactivation pattern in the liver of a manifesting female with ornithine transcarbamylase (OTC) deficiency, Clin Genet, 54, 349, 10.1034/j.1399-0004.1998.5440415.x

Egawa, 2004, Impact of age on outcome of ABO‐incompatible living donor liver transplantation, Transplantation, 77, 403, 10.1097/01.TP.0000110295.88926.5C

Miyagawa‐Hayashino, 2004, Outcome and risk factors of de novo autoimmune hepatitis in living‐donor liver transplantation, Transplantation, 78, 128, 10.1097/01.TP.0000132328.33460.43

Do, 2002, Benefits of chronic plasmapheresis and intravenous heme‐albumin in erythropoietic protoporphyria after orthotopic liver transplantation, Transplantation, 73, 469, 10.1097/00007890-200202150-00024

Dellon, 2002, Treatment of recurrent allograft dysfunction with intravenous hematin after liver transplantation for erythropoietic protoporphyria, Transplantation, 73, 911, 10.1097/00007890-200203270-00014

Van't Hoff, 1998, Combined liver‐kidney transplantation in methylmalonic academia, J Pediatr, 132, 1043, 10.1016/S0022-3476(98)70407-X

Bhattacharya, 2004, The benefits of liver transplantation in glycogenosis type Ib, J Inherit Metab Dis, 27, 539, 10.1023/B:BOLI.0000037400.49488.20

Chou, 2002, Type I glycogen storage diseases: disorders of the glucose‐6‐phosphate complex, Curr Mol Med, 2, 121, 10.2174/1566524024605798

Stankovics, 1994, Overexpression of human methylmalonic CoA mutase in mice after in vivo gene transfer with asialoglycoprotein/ polylysine/ DNA complexes, Hum Gene Ther, 5, 1095, 10.1089/hum.1994.5.9-1095

Richard, 2004, Hematopoietic stem cell gene therapy of murine protoporphyria by methylguanine‐DNA‐methyltransferase‐mediated in vivo drug selection, Gene Ther, 11, 1638, 10.1038/sj.gt.3302335

Broelsch, 1990, Application of reduced‐size liver transplants as split grafts, auxiliary orthotopic grafts and living related segmental transplants, Ann Surg, 212, 368, 10.1097/00000658-199009000-00015

Kasahara, 2003, Living‐donor liver transplantation with monosegments, Transplantation, 76, 694, 10.1097/01.TP.0000079446.94204.F9

Yersiz, 2003, One‐hundred in situ split‐liver transplantations: a single‐center experience, Ann Surg, 238, 496, 10.1097/01.sla.0000089852.29654.72

Ito, 2003, Surgery‐related morbidity in living donors of right‐lobe liver graft: lessons from the first 200 cases, Transplantation, 76, 158, 10.1097/01.TP.0000072372.42396.47

Akabayashi, 2004, The first donor death after living‐related liver transplantation in Japan, Transplantation, 77, 634, 10.1097/01.TP.0000115342.98226.7C

Plochl, 1999, Death after transplantation of a liver from a donor with unrecognized ornithine transcarbamylase deficiency, N Engl J Med, 341, 921, 10.1056/NEJM199909163411214