Spaide Richard F
From the Vitreous, Retina, Macula Consultants of New York, New York, NY.
Retina. 2025 Sep 3. doi: 10.1097/IAE.0000000000004662.
To reassess the anatomic basis of optic disc pit maculopathy (OPM) using swept-source optical coherence tomography (SS-OCT) and to characterize the broader structural abnormalities comprising the optic pit complex.
Sixteen patients with OPM were imaged using a high-resolution SS-OCT system (DREAM OCT). Cross-sectional and volume-rendered scans were analyzed for lamina cribrosa defects, intraneural cavitations, and pathways for fluid entry into or beneath the retina.
All eyes demonstrated lamina cribrosa defects with associated cavitations extending a mean of 1855 ± 492 µm posterior to a modified Bruch's membrane opening. Four distinct patterns by which fluid entered the retina were observed: (1) direct channels from cavitations into the retina, (2) perivascular hyporeflective spaces, (3) intraneural channels extending toward cystoid spaces, and (4) isolated retinal cysts without a visible interconnection. Vitreous remnants, trabecular structures, or disorganized connective tissue were found within the optic nerve pit in several eyes. In 13% of cases, the pit was not visible by ophthalmoscopy due to overlying tissue. These structural variations frequently coexisted, and associated abnormalities extended beyond the optic disc margins.
OPM is associated with a spectrum of deep optic nerve abnormalities, collectively termed the optic pit complex. The combination of laminar disruption, cavitations, and multiple anatomic conduits for fluid ingress broadens the morphologic understanding of this condition. SS-OCT enables visualization of structures not accessible by ophthalmoscopy and may improve diagnostic precision, guide treatment decisions, and clarify the diverse mechanisms contributing to fluid accumulation in OPM.
使用扫频光学相干断层扫描(SS-OCT)重新评估视盘小凹黄斑病变(OPM)的解剖学基础,并描述构成视盘小凹复合体的更广泛结构异常。
使用高分辨率SS-OCT系统(DREAM OCT)对16例OPM患者进行成像。对横断面和容积再现扫描进行分析,以评估筛板缺陷、神经内空洞以及液体进入视网膜内或视网膜下的途径。
所有患眼均显示筛板缺陷,并伴有空洞,空洞在改良的布鲁赫膜开口后方平均延伸1855±492μm。观察到液体进入视网膜的四种不同模式:(1)从空洞直接进入视网膜的通道;(2)血管周围低反射间隙;(3)向囊样间隙延伸的神经内通道;(4)无可见连接的孤立视网膜囊肿。在几只眼中,视神经小凹内发现了玻璃体残余物、小梁结构或紊乱的结缔组织。在13%的病例中,由于覆盖组织的遮挡,检眼镜检查无法看到小凹。这些结构变异经常共存,相关异常超出视盘边缘。
OPM与一系列深部视神经异常有关,统称为视盘小凹复合体。板层破坏、空洞形成以及多种液体进入的解剖通道的组合拓宽了对这种疾病的形态学认识。SS-OCT能够显示检眼镜检查无法观察到的结构,可能会提高诊断准确性,指导治疗决策,并阐明导致OPM中液体积聚的多种机制。