JAMA Ophthalmol. 2013 Oct;131(10):1275-87. doi: 10.1001/jamaophthalmol.2013.4056.
With the advent of more sophisticated imaging systems, such as spectral domain optical coherence tomography (SD-OCT), disruption of the inner segment/outer segment (IS/OS) band, and thinning of the outer nuclear layer (ONL) have been identified in association with acute macular neuroretinopathy (AMN).
To characterize a new SD-OCT presentation of AMN as a paracentral acute middle maculopathy and to describe multimodal imaging findings that implicate an underlying pathogenesis related to retinal capillary ischemia.
DESIGN, SETTING, AND PARTICIPANTS: Retrospective observational case series (January 1, 2012, to January 1, 2013) reviewing clinical and imaging data from 9 patients (11 eyes) with AMN at 6 tertiary referral centers. Lesions were classified as type 1 or 2 in relation to the SD-OCT location of the lesion above (type 1) or below (type 2) the outer plexiform layer (OPL) at 6 tertiary referral centers.
Of the 9 patients, 5 were female and 4 were male (mean age, 47.6 years; range, 21-65 years). All patients presented with an acute paracentral scotoma and demonstrated a classic dark gray paracentral lesion with near-infrared imaging. Visual acuity ranged from 20/15 to 20/30. Six eyes (5 patients) had type 1 SD-OCT lesions, also referred to as paracentral acute middle maculopathy, and 5 eyes (4 patients) had type 2 SD-OCT lesions. Although type 1 lesions lead to inner nuclear layer (INL) thinning, type 2 lesions resulted in ONL thinning. Type 2 lesions were always associated with significant outer macular defects, including disruption of the inner segment/outer segment and outer segment/retinal pigment epithelium bands, whereas type 1 lesions spared the outer macula.
Paracentral acute middle maculopathy may represent a novel variant of AMN that affects the middle layers of the macula above the OPL as diagnosed with SD-OCT imaging. Two types of AMN lesions may be seen with SD-OCT occurring above and below the OPL. Type 1 refers to hyperreflective bands in the OPL/INL region with subsequent INL thinning. Type 2 is hyperreflective bands in the OPL/ONL region with subsequent ONL thinning. Type 2 lesions may be associated with concomitant defects of the inner segment/outer segment layer. We propose that each of these lesions may be explained by occlusion of either the superficial capillary plexus (type 1) or deep capillary plexus (type 2) located in the innermost and outermost portion of the INL, respectively, immediately adjacent to each corresponding lesion type.
随着更复杂的成像系统(如光谱域光学相干断层扫描(SD-OCT))的出现,与急性黄斑神经视网膜病变(AMN)相关的内节/外节(IS/OS)带中断和外核层(ONL)变薄已经被识别。
描述 AMN 的一种新的 SD-OCT 表现为旁中心急性中黄斑病变,并描述多模态成像发现,这些发现提示与视网膜毛细血管缺血相关的潜在发病机制。
设计、设置和参与者:回顾性观察性病例系列研究(2012 年 1 月 1 日至 2013 年 1 月 1 日),在 6 个三级转诊中心审查了 9 名(11 只眼)AMN 患者的临床和成像数据。病变根据病变在 SD-OCT 中位于外丛状层(OPL)上方(1 型)或下方(2 型)的位置分为 1 型或 2 型。
9 名患者中,5 名女性,4 名男性(平均年龄 47.6 岁;范围 21-65 岁)。所有患者均表现为急性旁中心暗点,并表现出典型的暗灰色旁中心病变,具有近红外成像。视力范围从 20/15 到 20/30。6 只眼(5 名患者)有 1 型 SD-OCT 病变,也称为旁中心急性中黄斑病变,5 只眼(4 名患者)有 2 型 SD-OCT 病变。虽然 1 型病变导致内核层(INL)变薄,但 2 型病变导致外核层(ONL)变薄。2 型病变总是与明显的外黄斑缺陷相关,包括内节/外节和外节/视网膜色素上皮带的中断,而 1 型病变则幸免了外黄斑。
旁中心急性中黄斑病变可能代表 AMN 的一种新变体,在 SD-OCT 成像中影响 OPL 上方的黄斑中层。可能在 OPL 上方和下方的 SD-OCT 中看到两种 AMN 病变。1 型指的是 OPL/INL 区域的高反射带,随后 INL 变薄。2 型是 OPL/ONL 区域的高反射带,随后 ONL 变薄。2 型病变可能与内节/外节层的并发缺陷相关。我们提出,这些病变中的每一种都可以通过位于 INL 最内层和最外层的浅层毛细血管丛(1 型)或深层毛细血管丛(2 型)的阻塞来解释,这两种病变分别位于相应病变类型的正下方。