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Bilateral Syphilitic Optic Neuropathy with Secondary Autoimmune Optic Neuropathy and Poor Visual Outcome

机译:伴有自身免疫性继发性视神经病变和不良视力结局的双边梅毒视神经病变

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摘要

We describe the case of a 65-year-old man who suffered progressive visual loss despite appropriate treatment of ocular syphilis. Our patient initially presented with a unilateral 6th nerve palsy and associated double vision, which self-resolved over 6 months. His ophthalmic examination was otherwise normal. 12 months after the initial complaint, he represented with dyschromatopsia, reduced visual acuity, tonic pupils, and optic nerve atrophy. He tested positive for syphilis and was admitted for treatment of neurosyphilis with high-dose benzylpenicillin. Despite treatment, at a 4-month review his visual acuity remained poor and progression of optic nerve atrophy was noted alongside the development of bilateral central scotomas. Further testing was congruent with a diagnosis of autoimmune optic retinopathy. We propose this to be secondary to his syphilitic infection. Syphilis is known as the “great mimicker,” and despite being quite treatable, this case highlights ongoing complexity in the diagnosis and management of syphilis, unfortunately with a poor visual outcome.
机译:我们描述了一个65岁的男人,尽管对眼梅毒进行了适当的治疗,但仍进行性视力减退。我们的患者最初出现单侧第六神经麻痹并伴有双重视力,可在6个月内自行消退。否则他的眼科检查正常。初次投诉后12个月,他表现为色盲,视力下降,瞳孔强直和视神经萎缩。他的梅毒测试呈阳性,并被接受大剂量苄青霉素治疗神经梅毒。尽管进行了治疗,但在4个月的复查中,他的视力仍然很差,并且注意到视神经萎缩的进展以及双侧中央肌的发展。进一步的检查与自身免疫性视神经病变的诊断是一致的。我们建议这是继发于梅毒的继发感染。梅毒被称为“伟大的模仿者”,尽管可以治愈,但该病例突显了梅毒的诊断和管理工作的持续复杂性,不幸的是视觉效果差。

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