Pulseless (Takayasu) disease with ophthalmic manifestations.

J R Lewis, J S Glaser, N J Schatz, D G Hutson
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Abstract

Pulseless disease (PD) is a rare disorder in which inflammation of the aorta and its major branches leads to stenosis or occlusion of these arteries. It mainly affects young Oriental women, who suffer chronic ischemic injury to tissues of the brain, orbits, upper limbs, myocardium, and kidneys. The ophthalmologic features of pulseless disease tend to be late manifestations, and can include ischemia of the retina, choroid, and anterior segment. The inflammatory process may be reversed in early stages with systemic corticosteroids, but, more frequently, significant arterial stenosis necessitates arterial bypass surgery. A 59-year-old Caucasian woman with stenosis of all four major cervical arteries presented with recurrent blurred vision, syncope, mental obtundation, and a remarkable funduscopic appearance due to bilateral orbital hypoperfusion. Her acute symptoms improved slightly on high-dose systemic corticosteroids, and then resolved completely following arterial bypass surgery.

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以眼部为表现的无脉病。
无脉病(PD)是一种罕见的疾病,其中主动脉及其主要分支的炎症导致这些动脉狭窄或闭塞。它主要影响年轻的东方女性,她们的大脑、眼眶、上肢、心肌和肾脏组织遭受慢性缺血性损伤。无脉性疾病的眼科特征往往是晚期表现,可包括视网膜、脉络膜和前段缺血。炎症过程可能在早期通过全身皮质类固醇逆转,但更常见的是,明显的动脉狭窄需要动脉搭桥手术。一位59岁的白人女性,颈部四大动脉狭窄,表现为反复视力模糊,晕厥,精神迟钝,双侧眼眶灌注不足,眼底表现明显。她的急性症状在大剂量全身皮质类固醇治疗后略有改善,然后在动脉搭桥手术后完全消失。
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