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与结节性硬化症相关的侵袭性视网膜星形细胞瘤。

Aggressive retinal astrocytoma associated with tuberous sclerosis.

作者信息

Tomida Machiko, Mitamura Yoshinori, Katome Takashi, Eguchi Hiroshi, Naito Takeshi, Harada Takayuki

机构信息

Department of Ophthalmology, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima.

出版信息

Clin Ophthalmol. 2012;6:715-20. doi: 10.2147/OPTH.S31759. Epub 2012 May 9.

Abstract

We report the case of a patient with an aggressive retinal astrocytoma accompanied with macular edema and neovascular vessels, who was initially treated with intravitreal bevacizumab injections. A 24-year-old male presented to our clinic complaining of visual disturbance in his right eye. At 8 years of age, he had been diagnosed as having tuberous sclerosis complex. Fundus examination demonstrated a retinal tumor accompanied with marked neovascular vessels on the surface, retinal hemorrhage, and macular edema. After six monthly intravitreal bevacizumab injections, fundus examination demonstrated marked regression of the macular edema and neovascular vessels. Two months later, a vitreous hemorrhage developed which necessitated pars plana vitrectomy. After additional intravitreal bevacizumab injection for preventing intraoperative bleeding, vitrectomy with endophotocoagulation for the tumor was performed. The vitreous sample was obtained during vitrectomy, and we measured the vascular endothelial growth factor concentration by enzyme-linked immunosorbent assay. The surgically removed epiretinal neovascular membrane and biopsied retinal tumor expressed vascular endothelial growth factor, although several intravitreal bevacizumab injections led to a vitreous vascular endothelial growth factor concentration of undetectable levels. The clinical course and immunohistochemical analyses indicate that intravitreal bevacizumab monotherapy may have been insufficient to treat the aggressive retinal astrocytoma with macular edema and that laser photocoagulation or photodynamic therapy for the tumor should be considered following intravitreal bevacizumab injection in such cases.

摘要

我们报告了一例患有侵袭性视网膜星形细胞瘤并伴有黄斑水肿和新生血管的患者,该患者最初接受了玻璃体内注射贝伐单抗治疗。一名24岁男性因右眼视力障碍前来我院就诊。他8岁时被诊断患有结节性硬化症。眼底检查发现视网膜肿瘤,表面伴有明显的新生血管、视网膜出血和黄斑水肿。在每月进行6次玻璃体内注射贝伐单抗后,眼底检查显示黄斑水肿和新生血管明显消退。两个月后,发生了玻璃体积血,需要进行玻璃体切割术。在额外注射玻璃体内贝伐单抗以预防术中出血后,对肿瘤进行了玻璃体切割联合眼内光凝术。在玻璃体切割术中获取了玻璃体样本,我们通过酶联免疫吸附测定法测量了血管内皮生长因子的浓度。手术切除的视网膜前新生血管膜和活检的视网膜肿瘤均表达血管内皮生长因子,尽管多次玻璃体内注射贝伐单抗导致玻璃体内血管内皮生长因子浓度降至检测不到的水平。临床病程和免疫组织化学分析表明,单纯玻璃体内注射贝伐单抗可能不足以治疗伴有黄斑水肿的侵袭性视网膜星形细胞瘤,在这种情况下,玻璃体内注射贝伐单抗后应考虑对肿瘤进行激光光凝或光动力疗法。

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