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贝伐单抗联合化疗诱发的可逆性后部白质脑病综合征在结直肠癌中的情况

Reversible posterior leukoencephalopathy syndrome induced by bevacizumab plus chemotherapy in colorectal cancer.

作者信息

Wang Wei, Zhao Li-Rong, Lin Xiu-Qiang, Feng Fen

机构信息

Wei Wang, Li-Rong Zhao, Xiu-Qiang Lin, Fen Feng, Department of Gastroenterology, Foshan First People's Hospital, Foshan 520800, Guangdong Province, China.

出版信息

World J Gastroenterol. 2014 Jun 7;20(21):6691-7. doi: 10.3748/wjg.v20.i21.6691.

Abstract

Reversible posterior leukoencephalopathy syndrome (RPLS) is a rare brain-capillary leak syndrome, characterized by clinical symptoms of headache, visual loss, seizures and altered mental functioning. This syndrome is usually reversible and is associated with hypertension, nephropathy, and use of immunosuppressive medication and cytotoxic agents. We describe two rare cases of RPLS occurring in colorectal cancer, both of which presented with coma, that we believe can be directly attributed to bevacizumab, a monoclonal antibody that inhibits the angiogenesis of tumours by specifically blocking vascular endothelial growth factor. We analysed the clinical features, risk factors and outcomes of RPLS in these two patients, and although no typical finding was identified on imaging examination, we found that inadequate blood pressure control was one of the risk factors leading to RPLS and that supportive treatment including intensive blood pressure control improved outcomes. Due to the increasing use of bevacizumab in colorectal cancer, clinicians should be aware of this potential complication.

摘要

可逆性后部白质脑病综合征(RPLS)是一种罕见的脑毛细血管渗漏综合征,其特征为头痛、视力丧失、癫痫发作和精神功能改变等临床症状。该综合征通常是可逆的,与高血压、肾病以及免疫抑制药物和细胞毒性药物的使用有关。我们描述了两例发生在结直肠癌患者中的罕见RPLS病例,这两例患者均表现为昏迷,我们认为这可直接归因于贝伐单抗,一种通过特异性阻断血管内皮生长因子来抑制肿瘤血管生成的单克隆抗体。我们分析了这两名患者RPLS的临床特征、危险因素和结局,尽管在影像学检查中未发现典型表现,但我们发现血压控制不佳是导致RPLS的危险因素之一,包括强化血压控制在内的支持性治疗改善了结局。由于贝伐单抗在结直肠癌中的使用日益增加,临床医生应意识到这种潜在并发症。

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