Flutamide-induced hepatotoxicity: A case report

O. Kassid, S. Odhaib, M. Altemimi
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引用次数: 2

Abstract

Flutamide is a non-steroidal anti-androgen drug effective in the management of prostatic carcinoma. The drug appears to be well tolerated with mild gastrointestinal adverse events and gynecomastia. Flutamide-induced hepatotoxicity may range from minor elevation in liver enzymes to hepatic failure. Here, we tried to discuss the possibility of hepatotoxicity induced by flutamide as antiandrogen therapy in a patient with prostatic adenocarcinoma. Here we present a 75-year-old man who commenced flutamide as a postoperative anti-androgen for prostatic adenocarcinoma for two months. He had markedly elevated levels of liver enzymes due to acute liver failure and subsequent multi-organ failure. The patient died after the failure of the resuscitation measures. The temporal relationship between the flutamide initiation and the emergence of hepatotoxicity is not clear, with a possible latency of 12-16 weeks. Careful monitoring of liver function test during flutamide therapy is essential to prevent serious hepatotoxicity.
氟他胺致肝毒性1例报告
氟他胺是一种治疗前列腺癌的非甾体抗雄激素药物。该药耐受性良好,有轻微的胃肠道不良反应和男性乳房发育。氟他胺引起的肝毒性可从肝酶轻微升高到肝功能衰竭。在这里,我们试图讨论氟他胺作为抗雄激素治疗前列腺癌患者引起肝毒性的可能性。在这里,我们报告了一位75岁的男性,他开始使用氟他胺作为前列腺腺癌术后的抗雄激素治疗两个月。由于急性肝功能衰竭和随后的多器官功能衰竭,他的肝酶水平明显升高。病人在复苏措施失败后死亡。氟他胺起始与出现肝毒性之间的时间关系尚不清楚,可能潜伏期为12-16周。在氟他胺治疗期间仔细监测肝功能检查是必要的,以防止严重的肝毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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