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Acute visual loss and optic disc edema followed by optic atrophy in two cases with deeply buried optic disc drusen: a mimicker of atypical optic neuritis

机译:急性视觉损失和光盘水肿,后跟光学萎缩两种情况,深深埋藏光盘博森:非典型视神经炎的模仿者

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摘要

Abstract Background Sudden visual loss and optic disc edema caused by optic neuritis (ON) is usually followed by significant visual recovery. However, little or no recovery occurs when the loss is caused by atypical ON, especially in patients with neuromyelitis optica (NMO). Optic disc drusen (ODD) is a cause of pseudo optic disc edema and may be a predisposing factor for non-arteritic anterior ischemic optic neuropathy (NAION), thereby mimicking atypical ON. In such cases, if globular concretions are seen protruding from the disc substance, ODD may be suspected. The purpose of this paper is to describe two patients with acute visual loss followed by optic disc atrophy initially labeled as atypical ON. Though not suspected on clinical examination, optical coherence tomography (OCT) revealed deeply buried ODD as a predisposing factor for NAION. Case presentations Case 1: A 48-year-old woman had bilateral sequential visual loss associated with optic disc edema. Despite treatment, vision did not improve and severe disc pallor ensued. Atypical ON was suspected. Eventually, she was started on immunosuppressant therapy based on a tentative diagnosis of NMO-spectrum disorder. On examination 5 years later, only severe optic disc pallor was observed, but OCT radial B-scans showed ovoid hyporeflective areas in the retrolaminar region of both eyes, compatible with ODD; this led to a diagnosis of NAION and deeply buried ODD. Case 2. A 35-year-old woman with suspicion of ON in the left eye and a history of previous atypical ON in the right eye was referred for neuro-ophthalmic examination which revealed diffuse optic disc pallor and a dense arcuate visual field defect in the right eye. OCT B-scans passing through the disc showed large ovoid areas of reduced reflectivity in the retrolaminar region of the optic disc in the right eye. These findings helped confirm the diagnosis of NAION in one eye, with deeply buried ODD as predisposing factor. Conclusions Deeply buried ODD may be associated with NAION causing irreversible visual loss and optic disc pallor, a condition easily mistaken for atypical ON. Awareness of such occurrence is important to avoid unnecessary testing and minimize the risk of mismanagement.
机译:抽象背景突然视力丧失引起的视神经炎(ON)视神经乳头水肿通常随后为显著视力恢复。然而,当损失由非典型ON引起的,尤其是在患者的视神经脊髓炎(NMO)发生很少或没有恢复。视盘玻璃膜疣(ODD)是伪视盘水肿的原因,并且可以是用于非动脉前部缺血性视神经病(NAION)的诱发因素,从而模拟非典型ON。在这种情况下,如果球状结核被视为从盘突出的物质,ODD​​可以被怀疑。本文的目的是描述两种急性视力丧失,接着最初标记为非典型ON视盘萎缩。尽管临床检查不疑,光学相干断层扫描(OCT)揭示深埋ODD作为NAION的诱发因素。案例介绍案例1:一位48岁的妇女有视盘水肿相关双边顺序视力丧失。虽经治疗,视力没有改善,重度盘苍白接踵而至。非典型ON怀疑。最终,她开始基于NMO谱系疾病的初步诊断免疫抑制剂治疗。经检查,5年以后,只观察到严重的视神经乳头苍白,但华侨城径向B扫描显示,两只眼睛的筛板后区卵形hyporeflective领域,兼容光驱;这导致NAION的诊断和深埋ODD。病例2一位35岁的女子在左眼因涉嫌与以往非典型ON的右眼史被提到的显露弥漫性视神经乳头苍白和密集的弓形视野缺损的神经眼科检查右眼。通过该圆盘OCT B-扫描显示在右眼视盘的筛板后区域减小的反射率的大卵形区域。这些发现有助于确认NAION的诊断一只眼睛,用深埋ODD的诱发因素。深埋ODD结论可以与NAION造成不可逆的视力丧失和视神经盘苍白,容易误认为非典型ON的条件相关联。出现这样的意识是非常重要的,以避免不必要的测试,并尽量减少管理不善的风险。

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