© BMJ Publishing Group Limited 2022. No commercial reuse. See rights and permissions. Published by BMJ. DESCRIPTION A woman in her seventh decade of life presented with a 1day history… Click to show full abstract
© BMJ Publishing Group Limited 2022. No commercial reuse. See rights and permissions. Published by BMJ. DESCRIPTION A woman in her seventh decade of life presented with a 1day history of transient left eye pain and persistent welldemarcated round black scotoma in the left superotemporal visual field after bending down. The patient’s medical history was positive for obesity, but the patient had not seen her family physician for >5 years. Best corrected visual acuity (VA) was 6/6 in each eye. Anterior segments were unremarkable with normal intraocular pressures. There was no vitreous haemorrhage. The left fundus was remarkable for an approximately 15× disc area of subretinal haemorrhage (SRH) underlying the inferotemporal vascular arcades but sparing the fovea (figure 1A,B). There was no exudate, intraretinal or preretinal haemorrhage. Fundus fluorescein angiography (FFA, Spectralis, Heidelberg Engineering, Germany) highlighted a retinal artery macroaneurysm (RAM) along the inferotemporal arcades as well as superotemporal macular intraretinal telangiectasia (figure 1C,D). Optical coherence tomography (OCT, Spectralis) confirmed the subretinal nature and extent of SRH (figure 1E) with foveal sparing (figure 1F). Platelet count, prothrombin time and glycated haemoglobin level were all within normal limits. Blood pressure (BP) was 160/90 mm Hg and ambulatory 24 hour BP monitoring confirmed arterial hypertension. Treatment was initiated with intravitreal antivascular endothelial growth factor (antiVEGF, Ranibizumab, Novartis International AG, Switzerland) injections. Though improvement in SRH was noted (figure 2A,C) at 2 months, an inferotemporal branch retinal vein occlusion (BRVO) with cystoid macular oedema had developed reducing vision to 6/12 (figure 2D). Further, antiVEGF injections and control of arterial hypertension were carried out. RAMs are focal dilatations of retinal arterioles associated with hypertension. 2 They occur in approximately 1:4500 people with a 3:1 female preponderance. The suggested pathophysiology is that of arteriolosclerotic damage and remodelling leading to ≥1 focal aneurysmal dilatation(s) ranging from 100 to >250 μm in diameter often occurring at arteriovenous crossings or bifurcation sites and most commonly along the temporal vascular arcades. Lavin et al classified RAM into quiescent (ie, incidental), exudative (ie, slow leakage with intraretinal and subretinal lipid deposition) and haemorrhagic (ie, acute bleed into subretinal space ± intraretinal/vitreous components). Diagnosis is clinical with adjunctive FFA or indocyanine green angiography. Visual prognosis depends on the location of the aneurysm and the status at presentation (eg, incidental vs symptomatic) with inferior lesions harbouring a more favourable prognosis. Control of systemic hypertension is critical to mitigate visual loss secondary to RAM. Ophthalmic treatment modalities include focal laser techniques and/or intravitreal antiVEGF. 5 Success of RAM thrombosis following laser photocoagulation may be limited (~27%) and may result in aneurysm rupture or downstream ischaemia while antiVEGF therapy provides superior visual outcomes to observation. Management of SRH depends on location, duration and patient factors (eg, suitability for surgery). Observation of RAMassociated SRH is reasonable, particularly with inferior foveasparing lesions (VA ≥6/12 in 37%). RAMs have been reported at mean of 23 months following 7%–19% of BRVO, potentially as a Figure 1 (A,B) Multicolour fundus photographs (Spectralis, Heidelberg Engineering, Germany) of the patient’s left eye showing a large subretinal haemorrhage (SRH) surrounding a retinal artery macroaneurysm (RAM). (C,D) Fundus fluorescein angiography (FFA, Spectralis) highlighting masking of choroidal fluorescence by SRH with overlying RAM and leaking intraretinal focus in the superotemporal macula. (E) Optical coherence tomography (OCT, Spectralis) demonstrating the subretinal location of the haemorrhage. (F) OCT through the fovea demonstrating sparing by SRH.
               
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