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首页> 外文期刊>Case Reports in Ophthalmology >Treatment of Capillary Hemangioblastoma in Von Hippel-Lindau Disease: Case Report and Online Survey of Treatment Preferences among Experts
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Treatment of Capillary Hemangioblastoma in Von Hippel-Lindau Disease: Case Report and Online Survey of Treatment Preferences among Experts

机译:von Hippel-Lindau疾病中毛细血管血管母细胞瘤的治疗:专家案例报告及治疗偏好在线调查

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This case report aims to describe the diagnosis, treatment, and evolution of bilateral, asymmetrical retinal capillary hemangioblastomas treated with argon laser and intravitreal anti-vascular endothelial growth factor and also reports the results of an online survey of treatment preferences among retina and vitreous specialists. A previously healthy 23-year-old female presented to our Retina Department complaining of progressive visual loss in her right eye. Visual acuity at admission was 20/300 in her right eye and 20/20 in her left eye. Anterior segment findings were unremarkable and fundoscopy revealed the presence of retinal capillary hemangioblastomas in both eyes. In the right eye, the hemangioblastoma was associated with pronounced exudation and macular edema; in the left eye, the lesion was quiescent. After a complete anamnesis and genetic counseling, Von Hippel-Lindau disease was diagnosed. Treatment with laser photocoagulation was performed on both eyes. One dose of 0.5 mg intravitreal ranibizumab was applied to the right eye. Two months after treatment, the right eye demonstrated improved visual acuity (20/100). Moreover, an important decrease in tumor dimensions and a reduction of vessel tortuosity was seen in both eyes. At 18 months of follow-up, the patient maintains a good visual acuity without recurrence of the treated tumors. Laser treatment should be considered as the primary treatment option for patients with capillary hemangioblastomas with and without exudation and can be combined with intravitreal antiangiogenics if exudation is significant. Inactive smaller lesions without exudation are likely to have an excellent response to laser treatment alone. Management should be individualized since no consensus between experts has been reached.
机译:本案例报告旨在描述用氩激光和玻璃体抗体抗血管内皮生长因子治疗双侧,不对称视网膜毛细血管血管细胞母细胞瘤的诊断,治疗和演化,并报告了视网膜和玻璃体专家之间的在线调查的结果。一个以前健康的23岁女性介绍了我们的视网膜部门,抱怨她右眼的渐进视力丧失。入场院的视力是她右眼的20/300,左眼20/20。前段结果不起眼,基础镜检查显示两只眼中视网膜毛细血管血管母细胞瘤的存在。在右眼,血管母细胞瘤与发音渗出和黄斑水肿有关;在左眼,病变是静止的。经过完整的anamnesis和遗传咨询,von hippel-lindau疾病被诊断出来。用激光光凝治疗在两只眼睛上进行。将一剂0.5mg intraviteal ranibizumab施用于右眼。治疗后两个月后,右眼显示出改善的视力(20/100)。此外,两只眼睛都观察到肿瘤尺寸的重要降低和血管饼干的减少。在18个月的随访时,患者保持良好的视力,而不会复发治疗肿瘤。激光治疗应被视为毛细血管血管素母细胞瘤的初级治疗选择,如果渗出是显着的,可以与玻璃体抗体抗血管生物学结合。不渗出的无活性较小的病变可能对单独的激光治疗具有出色的反应。管理层应该是个性化,因为达到专家之间没有共识。

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