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血管内皮生长因子抑制剂眼内给药的全身和肾脏毒性。

Systemic and kidney toxicity of intraocular administration of vascular endothelial growth factor inhibitors.

机构信息

Service de néphrologie-transplantation rénale, Hôpital Foch, Suresnes, France.

出版信息

Am J Kidney Dis. 2011 May;57(5):756-9. doi: 10.1053/j.ajkd.2010.11.030. Epub 2011 Feb 4.

DOI:10.1053/j.ajkd.2010.11.030
PMID:21295897
Abstract

Intravenous injection of angiogenesis-inhibitor drugs is used widely to treat cancers. Associated renal complications primarily involve proteinuria and hypertension, and thrombotic microangiopathies also have been described. Intravitreal anti-vascular endothelial growth factor (VEGF) therapy currently is used by ophthalmologists to treat neovascularization in age-related macular degeneration. However, there is some evidence that intravitreal anti-VEGF injections may result in systemic absorption, with the potential for injury in organs that are reliant on VEGF, such as the kidney. We report the first case to our knowledge of a patient who developed an acute decrease in kidney function, nonimmune microangiopathic hemolytic anemia with schistocytes, and thrombocytopenia after 4 intravitreal injections of ranibizumab. Light microscopy of a kidney biopsy specimen showed segmental duplications of glomerular basement membranes with endothelial swelling and several recanalized arteriolar thrombi. Because of the increasing use of intravitreal anti-VEGF agents, ophthalmologists and nephrologists should be aware of the associated risk of kidney disease. Early detection is crucial so that intravitreal injections can be stopped before severe kidney disease occurs.

摘要

静脉注射血管生成抑制剂药物被广泛用于治疗癌症。相关的肾脏并发症主要涉及蛋白尿和高血压,也已描述过血栓性微血管病。眼科医生目前使用玻璃体内抗血管内皮生长因子 (VEGF) 疗法来治疗与年龄相关的黄斑变性的新生血管。然而,有一些证据表明,玻璃体内注射抗 VEGF 可能导致全身吸收,从而对依赖 VEGF 的器官造成损伤,如肾脏。我们报告了首例已知的患者病例,该患者在接受了 4 次雷珠单抗玻璃体内注射后,出现肾功能急性下降、非免疫性微血管性溶血性贫血伴裂体细胞和血小板减少症。肾脏活检标本的光镜检查显示肾小球基底膜的节段性重复,伴有内皮肿胀和几个再通的小动脉血栓。由于玻璃体内抗 VEGF 药物的使用越来越多,眼科医生和肾病学家应该意识到相关的肾脏疾病风险。早期发现至关重要,以便在严重的肾脏疾病发生之前停止玻璃体内注射。

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