Vela José Ignacio, Perich Sandra, Bulnes Victoria, Loscos Irene, Baradad María
Department of Opthalmology, Hospital de la Santa Creu i Sant Pau, Sant, Barcelona, Spain.
Department of Ophthalmology, Institut Condal d'Oftalmologia, Barcelona, Spain.
Neuroophthalmology. 2023 Feb 16;47(3):164-170. doi: 10.1080/01658107.2023.2176890. eCollection 2023.
Familial amyloid polyneuropathy is a rare autosomal dominant hereditary disease. Optic nerve involvement is frequently observed secondary to uncontrolled glaucoma but, rarely, an ischaemic optic neuropathy can occur. In this case report we describe a patient who presented with bilateral progressive visual loss and constriction of his visual fields. Fundus examination showed intense paleness of both optic discs with elevated, poorly defined margins that seemed to be infiltrated. Fundus autofluorescence and enhanced-depth imaging optical coherence tomography ruled out the presence of optic disc drusen. Orbital magnetic resonance imaging ruled out any sign of orbital compression, inflammation or infiltration of the optic nerve. The mechanism of small vessel amyloid infiltration and a possible vessel compression by amyloid in the optic nerve head is discussed.
家族性淀粉样多神经病是一种罕见的常染色体显性遗传病。视神经受累常继发于未控制的青光眼,但缺血性视神经病变很少见。在本病例报告中,我们描述了一名患者,他出现双侧进行性视力丧失和视野缩窄。眼底检查显示双侧视盘明显苍白,边缘隆起、边界不清,似乎有浸润。眼底自发荧光和增强深度成像光学相干断层扫描排除了视盘玻璃膜疣的存在。眼眶磁共振成像排除了眼眶压迫、炎症或视神经浸润的任何迹象。本文讨论了小血管淀粉样浸润的机制以及淀粉样物质对视神经乳头可能的血管压迫。