Singla Konica, Agarwal Prateek
Wills Eye Hospital
Cleveland Clinic Abu Dhabi
Optic ischemia, otherwise known as ischemic optic neuropathy, encompasses vascular diseases affecting the optic nerve. The condition is categorized into anterior and posterior types. Anterior ischemic optic neuropathies often present with optic disc edema, while posterior ones do not. Nonarteritic acute anterior ischemic optic neuropathy (NAION) is the most common form of optic ischemia, typically occurring in individuals with a small, crowded optic nerve. However, the exact cause of this disorder remains unknown, and curative or preventive treatment is not available. Posterior ischemic optic neuropathy is rare and typically associated with cardiovascular risk factors or perioperative conditions. This subset also lacks specific treatment. Urgent evaluation for arteritic causes, notably giant-cell arteritis (GCA), is essential, with immediate intravenous methylprednisolone administration indicated to limit vision loss in the affected eye and prevent involvement of the other eye. The optic nerve spans from the eyeball to the chiasm and has 4 segments: intraocular (1 mm), intra-orbital (30 mm), intracanalicular (6-10 mm), and intracranial (10-16 mm). Nerve fibers arise from retinal ganglion cells and converge at the optic disc, commonly known as "the blind spot," before traveling approximately 1 mm within the globe and penetrating the sclera through a sieve-like structure called "lamina cribrosa." Encased by the optic nerve sheath, the optic nerve also sits amid extraocular muscles and fat tissue. The optic nerve has a diameter of about 3 mm, while the optic nerve sheath measures approximately 1 mm thick. The sheath consists of the pia mater, subarachnoid space, arachnoid mater, and dura mater. This covering varies in thickness from 0.09 to 0.15 mm for the pia and arachnoid mater, to 0.1 to 0.29 mm for the subarachnoid space, and 0.3 to 0.5 mm for the dura. The subarachnoid space features a complex structure of trabeculae, septa, and pillars immersed in cerebral spinal fluid, with variations along the nerve's course. The optic nerve is divided into anterior and posterior portions and may be damaged by ischemia anywhere along its path. The optic nerve area between the retina and sclera is supplied by a network of 6 to 12 short posterior ciliary arteries at the back of the globe. These vessels form a circumferential network called the "circle of Zinn-Haller." The optic nerve head is perfused in a centripetal and segmental fashion. Branches from the pial plexus supply the optic nerve's retrolaminar portion. The anterior part contains trabeculae of 5 to 7 µm diameter, while the midsection exhibits septa and pillars dividing the space into communicating chambers, with pillars ranging from 10 to 30 µm in diameter. Both pillars and trabeculae are present in the posterior part, where the sheath traverses the optic canal. The right and left optic nerves cross each other within the cranium, forming the optic chiasm and connecting with the visual cortex within the occipital lobe.
视神经缺血,又称缺血性视神经病变,包括影响视神经的血管疾病。该病分为前部和后部类型。前部缺血性视神经病变常表现为视盘水肿,而后部则无。非动脉性急性前部缺血性视神经病变(NAION)是最常见的视神经缺血形式,通常发生在视神经细小、拥挤的个体中。然而,这种疾病的确切病因尚不清楚,也没有治愈或预防性治疗方法。后部缺血性视神经病变很少见,通常与心血管危险因素或围手术期情况有关。这一亚型也缺乏特异性治疗方法。对动脉性病因,尤其是巨细胞动脉炎(GCA)进行紧急评估至关重要,应立即静脉注射甲基强的松龙,以限制患眼视力丧失并防止另一只眼受累。视神经从眼球延伸至视交叉,有4个节段:眼内段(1毫米)、眶内段(30毫米)、管内段(6 - 10毫米)和颅内段(10 - 16毫米)。神经纤维起源于视网膜神经节细胞,在视盘(通常称为“盲点”)汇聚,然后在眼球内行进约1毫米,通过一个称为“筛板”的筛状结构穿透巩膜。视神经被视神经鞘包裹,也位于眼外肌和脂肪组织之间。视神经直径约3毫米,而视神经鞘厚度约1毫米。该鞘由软脑膜、蛛网膜下腔、蛛网膜和硬脑膜组成。软脑膜和蛛网膜的厚度在0.09至0.15毫米之间,蛛网膜下腔为0.1至0.29毫米,硬脑膜为0.3至0.5毫米。蛛网膜下腔具有浸入脑脊液中的小梁、隔膜和支柱的复杂结构,沿神经行程存在变化。视神经分为前部和后部,在其路径的任何部位都可能因缺血而受损。视网膜和巩膜之间的视神经区域由眼球后部6至12条睫状后短动脉组成的网络供血。这些血管形成一个称为“Zinn - Haller环”的圆周网络。视神经乳头以向心和节段性方式灌注。软膜丛的分支供应视神经的筛板后部分。前部含有直径为5至7微米的小梁,中部有隔膜和支柱将空间分隔成交通腔室,支柱直径为10至30微米。支柱和小梁在后部都存在,此处鞘穿过视神经管。左右视神经在颅腔内交叉,形成视交叉,并与枕叶内的视觉皮层相连。