Fernandes N F, Geller S A, Fong T L
Center for Liver Diseases and Transplantation and Department of Pathology and Laboratory Medicine, Cedars Sinai Medical Center, Los Angeles, California 90048, USA.
Am J Gastroenterol. 1998 Mar;93(3):459-60. doi: 10.1111/j.1572-0241.1998.00459.x.
We report a patient who developed significant liver dysfunction following therapy with terbinafine. At the end of a 3 1/2-wk course of terbinafine, he developed progressive jaundice and pruritus. His serum bilirubin peaked at 30.9 mg/dl 3 wk after discontinuing terbinafine. A liver biopsy revealed mild to moderate mixed cellular infiltrate in the portal tracts, and hepatocellular and canicular cholestasis. His liver tests normalized 100 days after stopping terbinafine.
我们报告了一名患者,其在接受特比萘芬治疗后出现了严重的肝功能障碍。在为期3.5周的特比萘芬疗程结束时,他出现了进行性黄疸和瘙痒。停用特比萘芬3周后,他的血清胆红素峰值达到30.9mg/dl。肝脏活检显示门管区有轻度至中度混合细胞浸润,以及肝细胞性和胆小管性胆汁淤积。停用特比萘芬100天后,他的肝功能检查恢复正常。