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环磷酰胺相关的肝毒性。

Cyclophosphamide-associated hepatotoxicity.

作者信息

Goldberg J W, Lidsky M D

出版信息

South Med J. 1985 Feb;78(2):222-3. doi: 10.1097/00007611-198502000-00034.

DOI:10.1097/00007611-198502000-00034
PMID:3975725
Abstract

Cyclophosphamide, a potent alkylating agent, is effective therapy for some rheumatic diseases. Despite primary hepatic activation of the drug, hepatic toxicity has been reported only in one case. We have reported two episodes of hepatic dysfunction associated with oral cyclophosphamide administration in patients with systemic rheumatic diseases.

摘要

环磷酰胺是一种强效烷化剂,对某些风湿性疾病是有效的治疗药物。尽管该药主要在肝脏激活,但仅报道过1例肝毒性病例。我们报告了2例系统性风湿性疾病患者口服环磷酰胺后出现肝功能障碍的情况。

相似文献

1
Cyclophosphamide-associated hepatotoxicity.环磷酰胺相关的肝毒性。
South Med J. 1985 Feb;78(2):222-3. doi: 10.1097/00007611-198502000-00034.
2
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Am J Transl Res. 2019 Oct 15;11(10):6444-6453. eCollection 2019.
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J Physiol Biochem. 2015 Sep;71(3):435-54. doi: 10.1007/s13105-015-0423-y. Epub 2015 Jul 14.
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Challenge of liver disease in systemic lupus erythematosus: Clues for diagnosis and hints for pathogenesis.
系统性红斑狼疮中肝脏疾病的挑战:诊断线索与发病机制提示
World J Hepatol. 2014 Jun 27;6(6):394-409. doi: 10.4254/wjh.v6.i6.394.
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Peroxisome Proliferator Activator Receptor (PPAR)- γ Ligand, but Not PPAR- α , Ameliorates Cyclophosphamide-Induced Oxidative Stress and Inflammation in Rat Liver.过氧化物酶体增殖物激活受体 (PPAR)-γ 配体,但不是 PPAR-α,可改善环磷酰胺诱导的大鼠肝氧化应激和炎症。
PPAR Res. 2014;2014:626319. doi: 10.1155/2014/626319. Epub 2014 Apr 2.
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Dose adaptation of antineoplastic drugs in patients with liver disease.肝病患者抗肿瘤药物的剂量调整
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Acute icteric hepatitis induced by a short course of low-dose cyclophosphamide in a patient with lupus nephritis.一名狼疮性肾炎患者因短期小剂量环磷酰胺诱发急性黄疸型肝炎。
Dig Dis Sci. 2005 Dec;50(12):2364-5. doi: 10.1007/s10620-005-3065-z.
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Reversible hepatic dysfunction in association with cyclophosphamide therapy.与环磷酰胺治疗相关的可逆性肝功能障碍。
Eur J Pediatr. 1995 May;154(5):411-2. doi: 10.1007/BF02072117.