Distinguishing Retinal Arteritis from Retinal Phlebitis
Retinal arteritis and phlebitis are differentiated primarily by fluorescein angiography findings: arteritis shows delayed arterial filling, arterial wall staining, and segmental arterial occlusion, while phlebitis demonstrates venous wall staining, perivenular hemorrhages, and irregular venous caliber with dilated segments. 1, 2
Clinical Presentation Patterns
Arteritis Features
- Arterial involvement strongly suggests infectious etiology (57.9% in infectious uveitis vs 11.2% in non-infectious), making this the most critical distinguishing feature 2
- Focal or elongated segmental arterial sheathing with vessel discontinuity 3
- Cotton-wool spots indicating focal ischemia 4, 3
- Sclerotic arterial segments with narrowed caliber 3
- Kyrieleis plaques (white deposits along vessels) 3
- More commonly associated with severe vision loss 3, 2
Phlebitis Features
- Venous involvement is more common in both infectious and non-infectious uveitis but less specific for etiology 2
- Perivenular hemorrhages as a hallmark finding 3
- Irregular venous caliber with alternating dilated and sclerotic segments 3
- Venous sheathing (white lines along vessel walls) 2
- Often bilateral presentation, particularly in isolated retinal vasculitis 5
- May progress to branch retinal vein occlusion at the site of inflammation 6
Fluorescein Angiography: The Definitive Test
FA is the confirmatory diagnostic test that definitively distinguishes arteritis from phlebitis 1, 7
Arteritis on FA
- Delayed retinal arterial filling in early phases 4, 3
- Arterial wall staining and leakage 2
- Retinal capillary nonperfusion in arterial distribution 4, 3
- Segmental arterial occlusion patterns 2
Phlebitis on FA
- Venous wall staining and leakage 2
- Delayed venous drainage 2
- Venous occlusion patterns (typically at non-arteriovenous crossing sites in isolated phlebitis) 6
- Macular edema from venous leakage 6, 5
Critical Etiologic Distinction
The presence of arteritis (especially inflammatory artery sheathing at 33.7% vs 0% and artery occlusion at 22.1% vs 3.7%) strongly indicates infectious uveitis and mandates urgent systemic workup 2
When Arteritis Predominates
- Pursue infectious workup aggressively: tuberculosis, syphilis, acute retinal necrosis, cytomegalovirus, fungal, bacterial 2
- Consider giant cell arteritis if patient >50 years with systemic symptoms (headache, jaw claudication, temporal tenderness) 4
- Obtain ESR and CRP urgently if GCA suspected 1
When Phlebitis Predominates
- Consider non-infectious causes: sarcoidosis, Behçet's disease, systemic lupus erythematosus 2, 5
- Evaluate for isolated retinal vasculitis (5.7% of all retinal vasculitis cases) 5
- Still exclude infectious causes, as phlebitis occurs in both groups 2
Ancillary Diagnostic Tools
OCT Findings
- Detects macular edema (common in phlebitis) 1, 8
- Shows inner retinal thickening and hyperreflectivity in acute arterial occlusion 4
- Quantifies structural damage but doesn't distinguish vessel type involved 1
Fundus Photography
- Documents vascular sheathing patterns and caliber changes 1, 7
- Tracks hemorrhage distribution (perivenular in phlebitis) 3
- Monitors disease progression over time 1
Common Diagnostic Pitfalls
- Vitreous cells may obscure retinal vascular details in arteritis, requiring high index of suspicion 3
- Peripheral vasculitis may be asymptomatic initially, requiring dilated peripheral examination 9
- Both arteritis and phlebitis can coexist in the same patient, particularly in infectious uveitis 2
- Isolated focal phlebitis can mimic branch retinal vein occlusion but occurs away from arteriovenous crossings 6
- FA carries rare but serious risks (1 in 200,000 mortality) and requires informed consent and emergency protocols 1, 7
Immediate Management Implications
Arteritis requires more urgent intervention due to higher risk of severe vision loss and potential systemic disease 3, 2
- Arteritis with suspected GCA: immediate high-dose corticosteroids before biopsy 4
- Infectious arteritis: targeted antimicrobial therapy based on etiology 2
- Phlebitis: systemic corticosteroids (82% of cases) with consideration for additional immunosuppression (27% of cases) 5
- Both conditions may require intravitreal therapy, panretinal photocoagulation, or vitrectomy depending on severity 5