J Korean Ophthalmol Soc > Volume 55(5); 2014 > Article
Journal of the Korean Ophthalmological Society 2014;55(5):785-788.
DOI: https://doi.org/10.3341/jkos.2014.55.5.785    Published online May 15, 2014.
Ocular Syphilis Presented as Occult Outer Retinopathy.
Sung Who Park, Jong Ho Park, Ik Soo Byon, Ji Eun Lee
1Department of Ophthalmology, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Korea. jlee@pusan.ac.kr
2Department of Ophthalmology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Korea.
3Medical Research Institute, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Korea.
잠복외망막병증의 형태로 나타난 안매독
박성후1,3⋅박종호1⋅변익수2⋅이지은1,3
Department of Ophthalmology, Pusan National University Hospital, Pusan National University School of Medicine1, Busan, Korea
Department of Ophthalmology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine2, Yangsan, Korea
Medical Research Institute, Pusan National University Hospital, Pusan National University School of Medicine3, Busan, Korea
Abstract
PURPOSE
To report a case of ocular syphilis presenting as occult outer retinopathy. CASE SUMMARY: A 42-year-old female presented with decreased visual acuity for one month in duration in the left eye. Her best-corrected visual acuity (BCVA) was 20/20 in the right eye and 20/250 in the left eye. There was no sign of inflammation in the anterior segment. Fundus examination showed no distinct abnormal findings including vitreous cell or haziness except mild diabetic retinopathy and subtle opacity of the macula. Spectral domain optical coherence tomography (OCT) showed a marked distortion of the inner segment-outer segment (IS-OS) junction in the photoreceptor layer without macular edema. Fluorescent angiography revealed diffuse subtle hyperfluorescence with microvasculitis in late phase. Full-field electroretinography (ERG) and multifocal ERG showed decreased amplitude; thus, acute zonal occult outer retinopathy (AZOOR) was considered as the diagnosis. Laboratory work-ups before steroid therapy revealed positive serology for active syphilis. One month after treatment with penicillin G (6 million international units per day for 14 days), best-corrected VA improved to 20/30, and restoration of the IS-OS junction was observed on OCT. CONCLUSIONS: Ocular syphilis may present as occult outer retinopathy resembling AZOOR, and serologic work-up is required to avoid misdiagnosis. In the present case, anatomical and functional recovery were obtained after antibiotic therapy.
Key Words: Occult outer retinopathy;Ocular syphilis;Retinitis


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