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肝癌原位肝移植后酪氨酸血症临床特征的消退。

Resolution of the clinical features of tyrosinemia following orthotopic liver transplantation for hepatoma.

作者信息

Van Thiel D H, Gartner L M, Thorp F K, Newman S L, Lindahl J A, Stoner E, New M I, Starzl T E

出版信息

J Hepatol. 1986;3(1):42-8. doi: 10.1016/s0168-8278(86)80144-1.

DOI:10.1016/s0168-8278(86)80144-1
PMID:3018074
Abstract

The clinical history before transplantation and subsequent clinical and biochemical course of 3 children and one adult with hereditary tyrosinemia treated by orthotopic hepatic transplantation is described. All four patients are now free of their previous dietary restrictions and appear to be cured of both their metabolic disease and their hepatic neoplasm.

摘要

本文描述了3名儿童和1名成人遗传性酪氨酸血症患者原位肝移植术前的临床病史以及术后的临床和生化病程。所有4名患者现已摆脱先前的饮食限制,代谢疾病和肝肿瘤似乎均已治愈。

相似文献

1
Resolution of the clinical features of tyrosinemia following orthotopic liver transplantation for hepatoma.肝癌原位肝移植后酪氨酸血症临床特征的消退。
J Hepatol. 1986;3(1):42-8. doi: 10.1016/s0168-8278(86)80144-1.
2
[Surgical excision of a hepatoma complicating chronic tyrosinemia (author's transl)].[慢性酪氨酸血症合并肝癌的手术切除(作者译)]
Arch Fr Pediatr. 1980 Mar;37(3):187-90.
3
Liver transplantation for tyrosinemia. A review of 10 cases from the University of Pittsburgh.酪氨酸血症的肝移植。匹兹堡大学10例病例回顾。
Dig Dis Sci. 1990 Jan;35(1):153-7. doi: 10.1007/BF01537237.
4
Liver transplantation for hereditary tyrosinemia in the presence of hepatocellular carcinoma.存在肝细胞癌情况下的遗传性酪氨酸血症的肝移植
Transplant Proc. 1989 Feb;21(1 Pt 2):2445-6.
5
Tyrosinaemia type I: orthotopic liver transplantation as the only definitive answer to a metabolic as well as an oncological problem.I型酪氨酸血症:原位肝移植是解决代谢及肿瘤问题的唯一确切办法。
J Inherit Metab Dis. 1989;12 Suppl 2:339-42. doi: 10.1007/BF03335416.
6
Early liver transplantation is indicated for tyrosinemia type I.对于Ⅰ型酪氨酸血症,建议早期进行肝移植。
J Pediatr Gastroenterol Nutr. 1991 Jul;13(1):10-5. doi: 10.1097/00005176-199107000-00002.
7
The occurrence of hepatoma in the chronic form of hereditary tyrosinemia.遗传性酪氨酸血症慢性形式中肝癌的发生。
J Pediatr. 1976 Mar;88(3):434-8. doi: 10.1016/s0022-3476(76)80259-4.
8
Liver transplantation in type I tyrosinemia.I型酪氨酸血症的肝移植
Transplant Proc. 1995 Aug;27(4):2301-2.
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Hereditary tyrosinemia type I (chronic form): pathologic findings in the liver.遗传性I型酪氨酸血症(慢性型):肝脏的病理表现
Hum Pathol. 1989 Feb;20(2):149-58. doi: 10.1016/0046-8177(89)90179-2.
10
Outcome of therapy of hereditary tyrosinemia.遗传性酪氨酸血症的治疗结果
Acta Paediatr Jpn. 1988 Aug;30(4):425-8. doi: 10.1111/j.1442-200x.1988.tb02532.x.

引用本文的文献

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Plasma succinylacetone is persistently raised after liver transplantation in tyrosinaemia type 1.血浆琥珀酰丙酮在 1 型酪氨酸血症肝移植后持续升高。
J Inherit Metab Dis. 2013 Jan;36(1):15-20. doi: 10.1007/s10545-012-9482-1. Epub 2012 Mar 29.
2
Renal function in tyrosinaemia type I after liver transplantation: a long-term follow-up.肝移植后I型酪氨酸血症患者的肾功能:长期随访
J Inherit Metab Dis. 2005;28(6):871-6. doi: 10.1007/s10545-005-0059-0.
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Imaging features of type 1 hereditary tyrosinemia: a review of 30 patients.1型遗传性酪氨酸血症的影像学特征:30例患者的回顾
Pediatr Radiol. 1996 Dec;26(12):845-51. doi: 10.1007/BF03178035.
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Liver transplantation in tyrosinaemia type I: the Groningen experience.
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Successful treatment of homozygous protein C deficiency by hepatic transplantation.肝移植成功治疗纯合子蛋白C缺乏症。
Lancet. 1988 Feb 27;1(8583):435-8. doi: 10.1016/s0140-6736(88)91231-7.
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Visceral pathology of hereditary tyrosinemia type I.I型遗传性酪氨酸血症的内脏病理学
Am J Hum Genet. 1990 Aug;47(2):317-24.
7
Liver transplantation for tyrosinemia. A review of 10 cases from the University of Pittsburgh.酪氨酸血症的肝移植。匹兹堡大学10例病例回顾。
Dig Dis Sci. 1990 Jan;35(1):153-7. doi: 10.1007/BF01537237.
8
Treatment of inherited metabolic disorders by liver transplantation.通过肝移植治疗遗传性代谢紊乱
J Inherit Metab Dis. 1991;14(4):604-18. doi: 10.1007/BF01797930.