巨细胞病毒视网膜炎伴有高眼压葡萄膜炎掩盖的全视网膜闭塞性血管病变:病例报告。

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Seongyong Jeong
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引用次数: 0

摘要

巨细胞病毒(CMV)视网膜炎是一种罕见的疾病,涉及眼前节的重叠表现极为罕见。我们报告了一名最初表现为持续性角膜水肿,后被诊断为巨细胞病毒视网膜炎的患者。一名 72 岁的男子因右眼眼压(IOP)无法控制到医院就诊。初次就诊时,眼压为 36 毫米汞柱,由于角膜水肿,眼底不清晰。光谱域光学相干断层扫描显示他患有旁中心急性中间黄斑病变(PAMM)。超宽视野荧光素血管造影检查发现了泛视网膜阻塞性血管病变。三周后,为解决持续的高眼压问题,患者接受了小梁切除术。角膜水肿改善后,观察到白斑样周边病变和银丝样视网膜血管。房水聚合酶链反应显示 CMV 阳性。患者接受了口服缬更昔洛韦和玻璃体内更昔洛韦的抗病毒治疗。尽管治疗了 4 个月,但最终视力仍无光感,角膜水肿和虹膜新生血管持续存在。我们描述了一例同时发生高眼压葡萄膜炎和巨细胞病毒视网膜炎的罕见病例。即使存在介质不透明,PAMM 的存在也可能是 CMV 视网膜炎的最初可识别迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytomegalovirus retinitis with panretinal occlusive vasculopathy concealed by hypertensive uveitis: a case report.

Cytomegalovirus (CMV) retinitis is a rare disease, and overlapping manifestations involving the anterior segment are extremely uncommon. We report a patient who initially presented with persistent corneal edema and was later diagnosed with CMV retinitis. A 72-year-old man with uncontrolled intraocular pressure (IOP) in his right eye visited a tertiary hospital. At initial presentation, the IOP was 36 mmHg and the fundus was not clear due to corneal edema. Spectral domain optical coherence tomography revealed paracentral acute middle maculopathy (PAMM). Panretinal obstructive vasculopathy was observed on ultra-widefield fluorescein angiography. Three weeks later, trabeculectomy was performed to resolve the persistently high IOP. Once corneal edema improved, a white patch-like peripheral lesion and silver wire-like retinal vasculature were observed. Polymerase chain reaction of the aqueous humor was positive for CMV. Oral valganciclovir and intravitreal ganciclovir were administered as antiviral therapies. Despite treatment for 4 months, the final visual acuity was no light perception, with persistent corneal edema and neovascularization of the iris. We describe a rare case of the simultaneous occurrence of hypertensive uveitis and CMV retinitis. The presence of PAMM could be an initial identifiable sign of CMV retinitis, even in the presence of media opacity.

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