Querques Giuseppe, Bocco Maria Cecilia Angulo, Soubrane Gisele, Souied Eric H
Department of Ophthalmology, Ospedali Riuniti, University of Foggia, Foggia, Italy.
Graefes Arch Clin Exp Ophthalmol. 2008 Feb;246(2):319-21. doi: 10.1007/s00417-007-0689-z. Epub 2007 Oct 13.
To describe a young patient with choroidal neovascularization, associated with Stargardt's disease, who underwent treatment with intravitreal ranibizumab.
A 26-year-old man with a diagnosis of Stargard's disease presented at our department for sudden decreased vison in his right eye (20/800). Upon a complete oplthamologic examination, including fluorescein angiography (FA), indocyanine green angiography (ICGA) and optical coherence tomography (OCT), the patient was diagnosed with subfoveal CNV of the right eye. Owing to the subfoveal localization of the CNV, intravitreal ranibizumab injection was performed on this young patient.
Three months after the last intravitreal injection of ranibizumab, fundus biomicroscopy, FA, ICGA and OCT revealed the CNV closure and total resolution of the associated cistoid macular edema and serous retinal detachment, with no recurrence and no complication from the intravitreal injection of ranibizumab. Visual acuity improved only to 20/400.
Intravitreal ranibizumab injection seems to induce total regression of CNV complicating Stargardt's disease. Further investigations are required to confirm our results.
描述一名患有与Stargardt病相关的脉络膜新生血管的年轻患者,该患者接受了玻璃体内注射雷珠单抗治疗。
一名诊断为Stargardt病的26岁男性因右眼视力突然下降(20/800)前来我院就诊。经过全面的眼科检查,包括荧光素血管造影(FA)、吲哚菁绿血管造影(ICGA)和光学相干断层扫描(OCT),该患者被诊断为右眼黄斑中心凹下脉络膜新生血管(CNV)。由于CNV位于黄斑中心凹下,因此对这名年轻患者进行了玻璃体内注射雷珠单抗治疗。
在最后一次玻璃体内注射雷珠单抗三个月后,眼底生物显微镜检查、FA、ICGA和OCT显示CNV闭合,相关的黄斑囊样水肿和浆液性视网膜脱离完全消退,未出现雷珠单抗玻璃体内注射的复发和并发症。视力仅提高到20/400。
玻璃体内注射雷珠单抗似乎可使Stargardt病并发的CNV完全消退。需要进一步的研究来证实我们的结果。