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Combined anterior and posterior scleritis associated with central retinal vein occlusion: a case report

机译:合并前,后巩膜炎与视网膜中央静脉阻塞相关的病例报告

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The purpose of this study is to report an uncommon presentation of anterior and posterior scleritis with central retinal vein occlusion We report a 30-year-old female presenting with unilateral anterior and posterior scleritis with concurrent central retinal vein occlusion, the subsequent work-up, and the management. The patient presented with decreased vision and extraocular and intraocular inflammatory signs in the left eye. At presentation, the best corrected visual acuity in the right eye (OD) was 20/20 and left eye (OS) was perception of light, with inaccurate projection of rays in all quadrants. Intraocular pressure was 12?mmHg in both eyes. OS showed mild proptosis with lid edema. Ocular movements were free and full in both eyes. The bulbar conjunctiva showed nodular anterior scleritis. OS showed mild vitreous haze with an exudative detachment at the posterior pole, disc edema with dilated, congested and tortuous veins and multiple dot blot hemorrhages, flame-shaped hemorrhages, and soft exudates throughout the posterior pole and mid-periphery An ultrasound B scan showed a large hypoechoic area in the sub-Tenon’s space (T-sign) suggestive of periocular fluid collection and thickened sclero–choroidal complex. Orbital ultrasound did not show evidence of any orbital mass or any increase in extraocular muscle thickness. Fundus fluorescein angiography showed few areas of pinpoint hyperfluorescence in the early phase with leakage in the late phase, leakage from the optic disc and vascular staining and pooling of dye in areas of exudative detachment in the late phases in the left eye. Systemic work-up was within normal limits. The patient responded well over the next month with systemic and topical steroids showing complete resolution of the scleritis and exudative retinal detachment. Simultaneous anterior and posterior scleritis with concurrent central retinal vein occlusion is a rare entity requiring prompt diagnosis and systemic work-up for efficient management
机译:这项研究的目的是报告前,后巩膜炎伴视网膜中央静脉阻塞的罕见情况。我们报道了一名30岁女性,前,后巩膜炎均伴有视网膜中央静脉阻塞,随后进行了检查,和管理。病人的视力下降,左眼眼外和眼内发炎。演讲时,右眼(OD)的最佳矫正视力为20/20,左眼(OS)为光的感知,所有象限中光线的投影都不准确。两只眼的眼内压为12?mmHg。 OS显示轻度的眼球突出,伴有眼睑浮肿。两只眼睛的眼球运动自由而饱满。球结膜显示结节性前巩膜炎。 OS显示轻度玻璃体混浊,在后极处有渗出性脱离,椎间盘水肿,静脉扩张,充血和曲折,在后极和中周遍及多点斑点出血,火焰状出血和软性渗出物在特农氏下腔(T-sign)中存在大的低回声区,提示眼周液收集和硬化性脉络膜增厚。眼眶超声未显示任何眼眶质量或眼外肌厚度增加的证据。眼底荧光素血管造影显示,早期阶段很少出现精确的高荧光区域,后期阶段出现渗漏,视盘渗漏以及左眼后期渗出性脱离区域的染料染色和血管聚集。全身检查在正常范围内。患者在接下来的一个月中全身和局部类固醇激素反应良好,显示出巩膜炎和渗出性视网膜脱离完全消失。同时发生巩膜前和后巩膜炎并发视网膜中央静脉阻塞是罕见的病因,需要及时诊断和全身检查才能有效治疗

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