消失的胆管综合征:替莫唑胺和左乙拉西坦诱发胆汁淤积性肝损伤的后遗症。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL BMJ Case Reports Pub Date : 2024-11-14 DOI:10.1136/bcr-2024-260830
Lindsey Martens, Olawale Babalola, Awais Aslam, Rabiah Ashraf
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引用次数: 0

摘要

在治疗胶质母细胞瘤方面,替莫唑胺(TMZ)-左乙拉西坦(LEV)联合疗法的疗效优于TMZ单药疗法,正逐渐成为一种主流疗法。虽然以前曾有过肝毒性病例,但还没有与 TMZ-LEV 联合用药相关的胆管消失综合征(VBDS)的报道。本病例报告详细描述了一名 50 多岁的男性患者最近完成了右额叶胶质母细胞瘤的 TMZ 和 LEV 治疗。3 天后,他出现无痛性黄疸、深色尿液和苍白粪便。实验室评估显示他患有明显的高胆红素血症和转氨酶炎。对黄疸的肝内外原因进行了广泛检查,但均无结果,因此有必要进行肝活检。肝脏病理检查显示,非特异性组织形态学模式提示药物引起的肝损伤和胆汁淤积,并伴有严重的导管减少症。确诊为 TMZ 和 LEV 引起的 VBDS。由于肝功能检查持续升高,患者在消化内科门诊随访了 6 个月,最后心脏骤停死亡。
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Vanishing bile duct syndrome: a sequela of temozolomide and levetiracetam-induced cholestatic liver injury.

Temozolomide (TMZ)-levetiracetam (LEV) combination therapy in glioblastoma management is gradually becoming a mainstay treatment given its superior effect compared with TMZ monotherapy. While there have been previous cases of hepatotoxicity, there are no prior reports of vanishing bile duct syndrome (VBDS) associated with TMZ-LEV combination use. This case report details a male in his 50s who had recently completed TMZ and LEV for right frontal lobe glioblastoma. He presented 3 days later with painless jaundice, dark urine and pale stools. Laboratory evaluation was remarkable for marked hyperbilirubinemia and transaminitis. Extensive work up for hepatic and extra-hepatic causes of jaundice was of no yield, thus necessitating a liver biopsy. Liver pathology showed a non-specific histomorphology pattern suggesting drug-induced liver injury and cholestasis with severe ductopenia. VBDS due to TMZ and LEV was diagnosed. The patient followed with the gastroenterology clinic over 6 months for persistently elevated liver function tests before suffering a fatal cardiac arrest.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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