EALES DISEASE
EALES DISEASE
- Idiopathic obliterative perivasculitis
- Unknown etiology
- Healthy young adult (97.6%) of Indian subcontinent
- Extensive retinal nonperfusion
- Perivascular sheathing
- Neovascularization of disc and retina
- Recurrent vitreous hemorrage
AETIOLOGY:
- Idiopathic
- Nontuberculous mycobacteria M. fortuitum and M. chelonae isolated from classical eales’ disease pt’s aqueous and ERM
- Higher phenotype frequency of HLA B5, DR1 and DR 4
- Probably this HLA predisposition could be responsible for the presence of sequestered mycobacterium
CLASSIFICATION:
- Periphlebitis of unknown aetiology
- Vasculitis with tuberculous chorio retinitis
CLINICAL FINDINGS:
- Avascular areas in the retina periphery
- Microaneurysms, dilatation of capillary channels, tortuosity of neighboring vessels
- Spontaneous chorioretinal scars.
- It is a diagnosis of exclusion, as many other retinal disorders can mimic Eales disease, especially conditions of retinal inflammation & detachment or neovascularization
- Both soft and hard exudates are seen in Eale’s disease
Physical Findings:
- The physical findings mostly involve the retina and vitreous.
- Vascular sheathing with adjacent nerve fiber layer hemorrhages is seen in most patients.
- The sheathing can manifest as thin white lines, limiting the blood column on both sides of the sheathed vessel to heavy exudative sheathing that can cause vascular occlusion.
- Although believed to affect primarily the retinal veins, others have reported the same prevalence of both venules and arterioles.
- The anterior chamber may exhibit cell and flare with keratic precipitates.
- Sudden, painless loss of vision & floaters in front of the eye
- Vitreous debris and cells often are seen, even in the absence of vitreous hemorrhage.
- Macular edema can occur in eyes with vascular sheathing, and it often is cystoid in nature.
- Epiretinal membranes with or without macular edema can compromise visual acuity.
- The etiology of the macular edema is thought to be associated with low-grade inflammation
- Peripheral nonperfusion is a typical feature of Eales disease
- Parachute lesions are seen in Eale’s disease
COMPLICATIONS:
- Branch retinal vein occlusion (BRVO) can be seen in patients with Eales disease and may be limited to one area or may be multifocal
- Neovascularization of the disc (NVD) or neovascularization elsewhere (NVE) in the retina is observed in up to 80% of patients with Eales disease.
- Cystoid macular edema can occur in patients with Eales disease due to increased capillary permeability.
- A posterior vitreous separation has been reported in 27% of patients with Eales disease
- Vestibuloauditory dysfunction Myelopathy, ischemic stroke, hemiplegia, and multifocal white matter abnormalities have been reported.
TREATMENT:
- Treatments include thyroid extract, osteogenic hormones, androgenic hormones, and systemic steroids.
- The antioxidant vitamins A, C, and E have been suggested recently as a possible therapy because antioxidizing enzymes are deficient in the vitreous samples of patients with Eales disease
- Argon laser is used in Eales’ disease
Exam Important
- Eales disease is Recurrent vitreous hemorrage
- Panretinal photocoagulation is done in Eales disease
- Eales disease is characterized by Recurrent retinal haemorrhage, Recurrent vitreous haemorrhage & Neovascularization
- Retinal detachment seen in Eale’s disease
- In a young patient presenting with recurrent vitreous hemorrhage, diagnosis is Eale’s disease.
- A 25 year old male presents withpainless sudden loss of vision, ocular and systemic examination is not contributory is diagnosed with Eale’s disease.
- Eales disease is Recurrent periphelbitis retina.
- Eale’s disease is Vitreous hemorrhage
- Eales’ disease is best treated with Steroids
- Argon laser is used in Eales’ disease
- Both soft and hard exudates are seen in Eale’s disease
- Parachute lesions are seen in Eale’s disease
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