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Histopathology of retinoblastoma eyes enucleated after intra-arterial chemotherapy

机译:在动脉内化疗后视网膜母细胞瘤眼的组织病理学

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To demonstrate histopathological findings in retinoblastoma eyes enucleated after intra-arterial chemotherapy (IAC) with special emphasis on vascular toxicity and local tumour control.Retrospective study with a consecutive series of 23 retinoblastoma eyes enucleated after IAC where histopathological work-up was available.From November 2010 to June 2019 23 eyes were enucleated after the attempt of eye salvaging therapy with IAC using melphalan. IAC was the first line treatment in nine and salvage treatment in 14 eyes. Doses of melphalan ranged from 3 to 7.5?mg, whereby a strict protocol with age-appropriate dosage was not used until 2015. The mean number of treatment cycles was 1.8. The main indications for enucleation were poor treatment response or tumour progression in 14 eyes, severe vascular complications in five eyes and a total exudative retinal detachment with amaurosis in the remaining four eyes. We found active disease in 15 eyes with an indication for adjuvant chemotherapy due to high risk factors for metastases in four eyes. To date none of these patients developed metastatic disease. Concerning vascular toxicity, we detected a central retinal artery occlusion in three eyes, severe vasculitis in another three, ischaemic outer retina atrophy and choroidal ischaemia in seven eyes with one eye developing a severe proliferative retinopathy.IAC is a highly effective treatment option for advanced retinoblastoma, but the described potential risks should be kept in mind. These include severe vascular complications, as well as the possibility of persisting vital tumour cells fulfilling high-risk criteria for adjuvant chemotherapy.
机译:在动脉内化疗(IAC)之后,以特殊强调血管毒性和局部肿瘤对照的特性化组织病理学发现。在IAC可获得组织病理学处理后,用连续的23种视网膜母细胞瘤眼睛进行了连续的23个视网膜母细胞瘤眼睛。 2010年至2019年6月23日眼睛在使用Melphalan的眼药治疗尝试后,眼睛在尝试后进行。 IAC是14只眼中的九次和抢救治疗的第一线治疗。 Melphalan的剂量范围为3至7.5μmg,由此未使用具有年龄合适的剂量的严格方案,直至2015年。治疗循环的平均数量为1.8。对雌激素的主要适应症是治疗反应或14只眼中的肿瘤进展,五次眼中严重的血管并发症,并且在剩下的四只眼睛中与Amaurosis的总渗出性视网膜脱离。我们发现15只眼中的活跃疾病,呈现出辅助化疗的指示由于四个眼中的转移危险因素。迄今为止,这些患者均未产生转移性疾病。关于血管毒性,我们在三个眼中检测到中央视网膜动脉闭塞,另外三个,缺血外视网膜萎缩和脉络膜缺血在七个眼中的一只眼睛发育出严重的增殖性视网膜病变,是一种高效的视网膜母细胞瘤,但应牢记所描述的潜在风险。这些包括严重的血管并发症,以及持续持续肿瘤细胞的可能性,满足佐剂化疗的高风险标准。

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