Clinical Reasoning: A Woman With Progressive Painless Sequential Monocular Vision Loss

Section 1

A 68-year-old woman with a history of diabetes mellitus type 2, depression, and migraines presented with painless, consecutive vision loss. She reported progressive monocular vision loss affecting the left eye 2 weeks before presentation to our institution. Giant cell arteritis was suspected because of an elevated erythrocyte sedimentation rate of 72 mm/h. Treatment included high-dose steroids, aspirin, and cilostazol. Biopsy of the left temporal artery was negative. MRI brain and CT angiogram of the head and neck were normal. One week later, while tapering prednisone, she awoke with severe central vision loss in her right eye. Examination revealed visual acuities of finger-counting in the periphery of both eyes (OU), with hand movement perceived centrally OU. Pupils reacted sluggishly to light bilaterally without evidence of a relative afferent pupillary defect. Light yellow macular placoid lesions were noted on the funduscopic examination OU (Figure 1A) with sharply delineated pigmentary changes on fundus autofluorescence OU (Figure 1B). The neurologic examination was relevant for decreased proprioception in the halluces bilaterally and absent Achilles and patellar reflexes bilaterally. Initial ophthalmic examination revealed retinal changes believed to be consistent with bilateral central retinal artery occlusion (CRAO). She subsequently developed right-sided hearing loss during admission.

• Download figure
• Open in new tab
• Download powerpoint

Figure 1 Fundus Photography, Fundus Autofluorescence, and Fluorescein Angiography

Placoid-like macular pigmentary changes are depicted on fundus photography (A) and fundus autofluorescence (B); the sharply delineated margin of the pigmentary change (indicative of the pathologically affected area) is seen. Note also patchy choroidal filling and disc leakage noted on fluorescein angiography (C). OD = right eye; OS = left eye.

Section 2

Ischemic, infectious, and autoimmune etiologies should be considered in the differential diagnosis for cases of rapidly consecutive vision loss associated with an abnormal retinal appearance. Ischemic etiologies can involve emboli causing central or branch retinal artery occlusions or vasculitides, such as giant cell arteritis (commonly) or Susac syndrome (rarely). A wide range of infectious etiologies should be considered, particularly in immunocompromised patients, including the family of herpesviruses, syphilis, tuberculosis, cytomegalovirus, toxoplasmosis, and Bartonella, among others. Systemic lupus erythematosus, Behcet disease, and sarcoid are relevant rheumatologic considerations.

Ophthalmologic evaluation can be critical in making the diagnosis. In particular, a slitlamp examination, fluorescein angiography (FA), and optical coherence tomography (OCT) frequently yield valuable information that is not ascertainable on the funduscopic examination, as described below. Identifying the pattern of abnormalities observed with these tests is crucial in conducting a comprehensive yet efficient workup. In cases of retinal artery occlusion, searching for an embolic source is required and MRI of the brain is valuable in determining whether cerebral ischemia is present and, if so, which vascular distributions are affected. MRI brain and audiometry are important when FA is suggestive of Susac syndrome. The presence of intraocular inflammation or retinal vasculitis merits a serologic investigation for the infectious and immune entities above, and in patients with coexisting neurologic deficits, lumbar puncture is a helpful adjunct.

A slitlamp examination can identify intraocular inflammation, which cannot be visualized on routine bedside fundoscopy. FA visualizes dye transit through the retinal vasculature and choroidal circulation, allowing for the differentiation between vaso-occlusive processes of either circulation or retinal vasculitis. OCT allows for visualization of the retinal layers and can help to distinguish processes such as central or branch retinal artery occlusions, which cause ischemia to only the inner two-third of the retina, from inflammatory or immune processes which can cause full-thickness retinitis or outer retinal processes which could not be easily differentiated from one another based on funduscopic examination alone.

In our patient's case, retinal changes were accompanied by inflammation of the anterior chamber and the vitreous humor OU, suggesting an infectious or immune etiology rather than a retinal artery occlusion. FA demonstrated patchy choroidal perfusion in the right eye, with targetoid hyperfluorescent punctate foci in both macula (Figure 1C). OCT demonstrated loss of the outer retinal layers, inconsistent with the earlier working diagnosis of bilateral CRAO (Figure 2A).

• Download figure
• Open in new tab
• Download powerpoint

Figure 2 OCT Before Treatment and 14 Months Post-treatment

This OCT (A) before treatment with intravenous penicillin demonstrates loss of the delineation of the outer retinal layers—the ELM, photoreceptor layers, and RPE layers—which can be visually differentiated from one another in the healthy eye—and are here supplanted by a single, hyper-reflective layer. These changes correlate with loss of the retina peripheral to the ellipsoid zone on OCT, specifically including the RPE and photoreceptor layers. This OCT (B) from 14 months post-treatment with intravenous penicillin now demonstrates visible delineation between the outer retinal layers, including the ELM, the photoreceptor layers, and the RPE. BM = Bruch membrane; ELM = external limiting membrane; ILM = internal limiting membrane; OCT = optical coherence tomography; RPE = retinal pigment epithelium.

Section 3

Syphilis was the highest diagnosis on our differential based on the macular placoid lesions on fundoscopic examination, the patchy choroidal filling on FA, the loss of the outer retinal layers on OCT, hearing loss, and decreased proprioception in the halluces bilaterally suggestive of tabes dorsalis. Lumbar puncture was significant for 16 nucleated cells (33% polymorphonuclear leukocytes and 37% lymphocytes), 14 red blood cells, protein of 65 mg/dL, and glucose of 98 mg/dL. CSF venereal disease research laboratory (VDRL), serum treponemal antibodies, and serum rapid plasma reagin (RPR) were positive (the latter at a titer of 1:512), confirming a diagnosis of syphilis. The patient completed a 14-day course of 4 million units of intravenous penicillin G every 4 hours (24 million units daily). Repeat ophthalmic examination at 14 months post-treatment was significant for normal visual acuities (20/20) bilaterally and well-defined outer retinal layers on OCT (Figure 2B). She continued to have superonasal visual field loss in her right eye.