Reversible Posterior Leukoencephalopathy Syndrome in Patients Undergoing Chemotherapy for Solid Tumors. A Case Report and Review of the Literature

Konstantinos Tsapakidis, Vasilis Papadopoulos, T. Nikolaos, P. Michailidis, Chrysoula Doxani, K. Kamposioras
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Abstract

Introduction: Reversible posterior leukoencephalopathy syndrome (RPLS) is a clinical entity of subtle onset of headaches, seizures, impaired vision and usually acute hypertension associated with characteristic neuroimaging findings of subcortical oedema affecting the posterior cerebral circulation. In the last two decades the causative relationship of cytotoxic and targeted antineoplastic agents with RPLS is increasingly recognized among cancer patients. Material and Methods: Herein we present a case of advanced gastric cancer that developed RPLS after treatment with the combination of chemotherapy and Trastuzumab. A comprehensive review of the English literature and the association of cytotoxic agents used in the treatment of solid tumors, with RPLS is analyzed. Results: 65 cases, median age 54.2 years, mainly female (83%) developed RPLS after chemotherapy-based treatment. Colorectal and lung cancer was the most frequent diagnosis, while platinum and gemcitabine based treatment was commonly related with the syndrome. Hypertension, seizures, headache and visual disturbance were the usual presenting symptoms. In the majority of the cases symptoms improved partially or completely in average in average 6.5 days after conservative management. Complete radiologic resolution of the symptoms was observed in 4.2 weeks in 57,5% of the cases and partial improvement in 2.6 weeks (42,5% of the cases). Conclusions: Combination or single-agent chemotherapy as well as novel anticancer drugs are associated with RPLS. Clinicians need to have a high index of suspicion and the combination of the clinical picture with the characteristic neuroimaging findings can help in the prompt diagnosis. RPLS can be reversible with appropriate supportive treatment and discontinuation of the causative factors.
实体瘤化疗患者的可逆性后脑白质病综合征。一例病例报告及文献回顾
简介:可逆性后脑白质病综合征(RPLS)是一种临床症状,表现为轻微的头痛、癫痫发作、视力受损和急性高血压,并伴有影响后脑循环的皮质下水肿的特征性神经影像学表现。在过去的二十年中,细胞毒性和靶向抗肿瘤药物与RPLS的因果关系在癌症患者中得到越来越多的认识。材料和方法:在此,我们报告了一例晚期胃癌在化疗和曲妥珠单抗联合治疗后发生RPLS的病例。全面回顾英文文献和关联的细胞毒性药物用于治疗实体肿瘤,与RPLS分析。结果:65例患者,中位年龄54.2岁,以女性为主(83%),经化疗后发生RPLS。结直肠癌和肺癌是最常见的诊断,而铂和吉西他滨为基础的治疗通常与该综合征有关。高血压、癫痫、头痛和视力障碍是常见的症状。大多数病例在保守治疗后的平均6.5天内症状部分或完全改善。52.5%的病例在4.2周内症状完全缓解,在2.6周内部分改善(42.5%)。结论:联合或单药化疗以及新型抗癌药物与RPLS相关。临床医生需要有高度的怀疑指数,结合临床图片和特征性的神经影像学发现可以帮助及时诊断。通过适当的支持性治疗和停止致病因素,RPLS是可逆的。
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