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阿扎胞苷所致的快速起病性肝损伤可能是通过一种独特的肝脏低灌注机制。

Rapid Onset Liver Injury Due to Azacitidine Through Possibly a Unique Mechanism of Hypoperfusion of the Liver.

作者信息

Hatipoglu Dilara, Jamali Arsia, Sheng Emily, Reddy K Rajender

机构信息

University of Pennsylvania, Philadelphia, USA.

出版信息

J Investig Med High Impact Case Rep. 2025 Jan-Dec;13:23247096251344720. doi: 10.1177/23247096251344720. Epub 2025 May 21.

Abstract

Azacitidine and venetoclax are important anti-neoplastic agents used in the treatment of acute myeloid leukemia. Azacitidine has been implicated to cause nonhepatic ischemic injury. Here we report a case of severe, short latency drug-induced liver injury following the infusion of azacitidine and venetoclax in a patient which was subsequently mitigated through pretreatment with a vasodilatory agent.

摘要

阿扎胞苷和维奈克拉是用于治疗急性髓系白血病的重要抗肿瘤药物。阿扎胞苷已被认为可导致非肝脏缺血性损伤。在此,我们报告一例患者在输注阿扎胞苷和维奈克拉后发生严重的、潜伏期短的药物性肝损伤病例,该损伤随后通过使用血管扩张剂预处理得到缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71c9/12099081/133ea30bddaf/10.1177_23247096251344720-fig1.jpg

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