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聚乙二醇化脂质体阿霉素相关的肾局限性血栓性微血管病继发急性肾损伤

Acute Kidney Injury Secondary to Pegylated Liposomal Doxorubicin-Associated Renal-limited Thrombotic Microangiopathy.

作者信息

Karam Tarek S, Sarkar Mrinalini, Zuckerman Jonathan E

机构信息

Department of Nephrology, University of California, Los Angeles Medical Center, Los Angeles, CA.

Department of Pathology and Laboratory Medicine, University of California, Los Angeles Medical Center, Los Angeles, CA.

出版信息

Kidney Med. 2025 Mar 19;7(5):100998. doi: 10.1016/j.xkme.2025.100998. eCollection 2025 May.

Abstract

The emergence of pegylated liposomal doxorubicin (PLD) as a preferred treatment for various malignancies, because of its reduced cardiotoxicity compared with conventional doxorubicin, has raised significant interest. However, the association between PLD and thrombotic microangiopathy (TMA) remains a concerning and relatively rare complication. Here, we present the case of an 80-year-old man with metastatic Kaposi sarcoma who underwent extended PLD monotherapy, subsequently developing kidney-limited TMA demonstrated on kidney biopsy. This led to acute kidney injury necessitating hemodialysis. The patient's clinical history, laboratory, and kidney biopsy data supported PLD chemotherapy as the primary etiologic factor for the observed kidney-limited TMA, an insidious condition with poor prognosis. This report highlights the need for vigilance and early kidney biopsy in patients with rising serum creatinine concentrations or worsening proteinuria/hematuria during PLD therapy. Understanding the mechanisms underlying PLD-induced TMA, likely involving reactive oxygen species-mediated endothelial dysfunction and platelet aggregation, remains a crucial area for future research to optimize monitoring and management strategies for this rare yet severe complication associated with PLD therapy.

摘要

聚乙二醇化脂质体阿霉素(PLD)因其与传统阿霉素相比心脏毒性降低,已成为各种恶性肿瘤的首选治疗方法,这引起了人们的极大兴趣。然而,PLD与血栓性微血管病(TMA)之间的关联仍然是一种令人担忧且相对罕见的并发症。在此,我们报告一例80岁转移性卡波西肉瘤男性患者,接受了延长的PLD单药治疗,随后肾活检显示出现了局限于肾脏的TMA。这导致了急性肾损伤,需要进行血液透析。患者的临床病史、实验室检查和肾活检数据支持PLD化疗是观察到的局限于肾脏的TMA的主要病因,这是一种预后不良的隐匿性疾病。本报告强调,在接受PLD治疗期间血清肌酐浓度升高或蛋白尿/血尿恶化的患者中,需要保持警惕并尽早进行肾活检。了解PLD诱导TMA的潜在机制,可能涉及活性氧介导的内皮功能障碍和血小板聚集,仍然是未来研究的关键领域,以优化对这种与PLD治疗相关的罕见但严重并发症的监测和管理策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aaf/12049883/263e851a927f/gr1.jpg

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