Max Rady College of Medicine (ARV), Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada; Division of Ophthalmology (LD), Department of Surgery, McMaster University, Hamilton, Canada; Department of Ophthalmology and Vision Sciences (JAM, EAM), Toronto Western Hospital, University Health Network, University of Toronto, Toronto, Canada; and Division of Neurology (JAM, EAM), Department of Medicine, University of Toronto, Toronto, Canada.
J Neuroophthalmol. 2024 Sep 1;44(3):355-359. doi: 10.1097/WNO.0000000000001950. Epub 2023 Jul 21.
The clinical features of maculopathies and optic neuropathies often overlap: Both present with decreased visual acuity and variable loss of color vision; thus, maculopathy can be misdiagnosed as optic neuropathy, leading to patient harm. We aimed to determine what findings and/or tests were most helpful in differentiating between optic neuropathy and maculopathy.
A retrospective chart review of consecutive patients over 4.5 years who were referred to neuro-ophthalmology clinics with the diagnosis of optic neuropathy but whose final diagnosis was maculopathy. Patient demographics, mode of presentation, clinical profile, complete ophthalmological examination, results of all ancillary testing, and final diagnosis were recorded.
A total of 47 patients (27 women) were included. The median age was 55 years (range, 18-85). Most referrals were by ophthalmologists (72.3%) and optometrists (12.8%). The diagnosis of maculopathy was made in 51.1% of patients at the time of first neuro-ophthalmic consultation. Only 6.4% patients (3) had relative afferent pupillary defect. Benign disc anomalies (tilted, myopic, small, or anomalous discs) were present in 34.0%, and 21.3% had pathologic disc changes unrelated or secondary to maculopathy. Macular ocular coherence tomography (OCT) was abnormal in 84.4% (with outer retinal pathology in 42.2% and inner retina pathology in 17.8%). Retinal nerve fiber layer (RNFL) thickness was normal in 82.6% of patients.
Macular OCT is a high-yield test in differentiating between optic neuropathy and maculopathy and should be obtained in patients with suspected optic neuropathies who have normal RNFL thickness. Macular dystrophies, particularly cone dystrophies, unspecified retinal disorders, and macular degeneration were the most common mimics of optic neuropathy. The diagnosis was often present on OCT of the macula. The presence of coexistent benign and pathological disc anomalies may lead to maculopathy being misdiagnosed as optic neuropathy.
黄斑病变和视神经病变的临床特征经常重叠:两者都表现为视力下降和色觉不同程度的丧失;因此,黄斑病变可能被误诊为视神经病变,导致患者受到伤害。我们旨在确定哪些发现和/或检查最有助于区分视神经病变和黄斑病变。
对过去 4.5 年中因视神经病变被转诊至神经眼科诊所但最终诊断为黄斑病变的连续患者进行回顾性图表审查。记录患者的人口统计学、表现方式、临床特征、全面眼科检查、所有辅助检查结果和最终诊断。
共纳入 47 名患者(27 名女性)。中位年龄为 55 岁(范围 18-85 岁)。大多数转诊来自眼科医生(72.3%)和验光师(12.8%)。黄斑病变的诊断在首次神经眼科会诊时做出的占 51.1%。只有 6.4%的患者(3 人)存在相对性传入性瞳孔障碍。良性盘异常(倾斜、近视、小或异常盘)存在于 34.0%的患者中,21.3%的患者存在与黄斑病变无关或继发于黄斑病变的病理性盘改变。84.4%的患者黄斑区光学相干断层扫描(OCT)异常(外层视网膜病变占 42.2%,内层视网膜病变占 17.8%)。82.6%的患者视网膜神经纤维层(RNFL)厚度正常。
黄斑 OCT 是区分视神经病变和黄斑病变的高灵敏度检查,对于怀疑患有视神经病变且 RNFL 厚度正常的患者,应进行该检查。黄斑营养不良,特别是圆锥营养不良、未特指的视网膜疾病和黄斑变性是最常见的视神经病变模拟疾病。诊断通常在黄斑 OCT 上出现。同时存在良性和病理性盘异常可能导致黄斑病变被误诊为视神经病变。