与lenvatinib治疗相关的血栓性微血管病。

Macarena Contreras Angulo, Belén García Izquierdo, Laura Armengod Grao, Nuria Palacios García
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引用次数: 0

摘要

摘要:全身性血栓性微血管病(TMA)是一种严重的疾病,早期治疗对降低发病率和死亡率至关重要。仅累及肾脏的TMA与酪氨酸激酶抑制剂有关,包括lenvatinib,一种用于某些晚期肿瘤的药物。迄今为止,与该药物相关的系统性TMA尚未被描述。我们提出的情况下,患者进展性转移甲状腺癌谁开发了这种并发症后,开始与lenvatinib治疗。我们描述了导致诊断的体征和症状以及恢复所需的治疗。学习要点:血栓性微血管病(TMA)是一组以内皮损伤引起的毛细血管和小动脉血栓形成为特征的疾病。局部形式和系统形式都有描述。TMA累及全身的特点是溶血性贫血、低血小板和器官损害。血管内皮生长因子信号抑制剂与TMA相关,要么局限于肾脏,要么累及全身。Lenvatinib很少与TMA相关。虽然迄今为止只描述了孤立的或主要累及肾脏的形式,但也可能出现主要的全身形式。lenvatinib诱导的系统性TMA必须通过测量ADAMTS-13来区分。治疗包括停药和支持措施。当接受lenvatinib治疗的患者同时存在贫血和血小板减少症时,建议进行外周血涂片以排除TMA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Thrombotic microangiopathy associated with lenvatinib therapy.

Thrombotic microangiopathy associated with lenvatinib therapy.

Thrombotic microangiopathy associated with lenvatinib therapy.

Summary: Systemic thrombotic microangiopathy (TMA) is a serious condition whose early treatment is essential to reduce morbidity and mortality. TMA with only renal involvement has been associated with tyrosine kinase inhibitors, including lenvatinib, a drug used for certain advanced neoplasms. To date, TMA with systemic involvement associated with this drug has not been described. We present the case of a patient with progressive metastatic thyroid cancer who developed this complication after starting treatment with lenvatinib. We describe the signs and symptoms that led to the diagnosis and the treatment required for her recovery.

Learning points: Thrombotic microangiopathy (TMA) is a group of disorders characterized by thrombosis in capillaries and arterioles due to an endothelial injury. Both, localized and systemic forms have been described.TMA with systemic involvement is characterized by hemolytic anemia, low platelets, and organ damage.Vascular endothelial growth factor signaling inhibitors have been associated with TMA, either restricted to the kidney or with systemic involvement.Lenvatinib has been rarely associated with TMA. Although only forms with isolated or predominantly renal involvement had been described so far, a predominantly systemic form can occur.Lenvatinib-induced systemic TMA must be distinguished from primary forms by measuring ADAMTS-13. Treatment includes discontinuation of the drug and supportive measures.When anemia and thrombocytopenia coexist in a patient receiving treatment with lenvatinib, a peripheral blood smear to exclude TMA is recommended.

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