Pournaras J-A C, Vaudaux J D, Borruat F-X
Jules Gonin Eye Hospital, University of Lausanne, Lausanne, Switzerland.
Klin Monbl Augenheilkd. 2007 Apr;224(4):337-9. doi: 10.1055/s-2007-962950.
Neuro-ophthalmic findings are uncommon in the setting of Sjögren syndrome. We report the case of a patient with bilateral, sequential optic neuropathy as the initial manifestation of Sjögren syndrome.
A 38-year-old male presented with sudden painless visual loss in his left eye in May 2005. Fundus examination revealed a left swollen optic disk. Magnetic resonance imaging (MRI) revealed a left optic nerve lesion. Elevated titres of autoantibodies (ANA, anti-SSA, anti-SSB) were found, suggestive of Sjögren syndrome. In January 2006, he presented with painful sudden visual loss in the right eye. Fundus examination revealed a right swollen optic disk and left optic nerve atrophy. MRI was normal. Other aetiologies were ruled out.
Each episode was treated with intravenous methylprednisolone (1 g/day during 3 days), followed by oral prednisone (1 mg/kg/day). Moderate improvement of vision ensued in both eyes.
Atypical presentation of an optic neuropathy must raise the suspicion of an unusual aetiology. Our case illustrates how a bilateral sequential optic neuropathy in an otherwise healthy patient can result from an unusual inflammatory aetiology: primary Sjögren syndrome.
神经眼科表现在干燥综合征中并不常见。我们报告一例以双侧相继性视神经病变为干燥综合征初始表现的患者。
一名38岁男性于2005年5月出现左眼突发无痛性视力丧失。眼底检查显示左侧视盘肿胀。磁共振成像(MRI)显示左侧视神经病变。发现自身抗体(抗核抗体、抗SSA、抗SSB)滴度升高,提示干燥综合征。2006年1月,他出现右眼疼痛性突发视力丧失。眼底检查显示右侧视盘肿胀及左侧视神经萎缩。MRI正常。排除了其他病因。
每次发作均给予静脉注射甲泼尼龙(3天内每日1 g),随后口服泼尼松(每日1 mg/kg)。双眼视力均有中度改善。
视神经病变的非典型表现必须引起对不寻常病因的怀疑。我们的病例说明了一名原本健康的患者双侧相继性视神经病变是如何由一种不寻常的炎症病因即原发性干燥综合征引起的。