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ABSTRACT Frosted branch angiitis is a rare and severe form of retinal vasculitis. It may be idiopathic or arise secondary to a systemic disease. We have reported here an unusually severe case of frosted branch angiitis in a previously healthy 13-year old girl who presented with significantly reduced vision in both eyes. In this case, frosted branch angiitis was one of the presentations of systemic lupus erythematosus. The characteristic patterns of frosted branch angiitis were observed on fundoscopy in both eyes. An extensive etiological study was conducted, whereby the diagnosis of systemic lupus erythematosus was confirmed. Only a few such cases have been reported so far in the literature.
RESUMO A angeíte congelada é tipo específico de vasculite retiniana rara e grave. Pode ser idiopática ou secundária à doença sistêmica. Relatamos um incomum caso com associação ao lúpus eritematoso sistêmico, sendo a angeíte congelada uma das manifestações do quadro. Uma jovem de 13 anos, previamente hígida, apresentou queixa de baixa visual importante bilateral. À fundoscopia foi evidenciado o aspecto de angeíte de vasos congelados em ambos os olhos. Extensa investigação etiológica foi realizada com diagnóstico confirmado de lúpus eritematoso sistêmico. Poucos casos foram descritos na literatura.
RESUMO
Objective To observe the clinical features and treatment outcomes of presumed tubercular retinal vasculitis.Methods This is a retrospective non-comparative interventional clinical research.A total of nine patients (11 eyes) with major presentation of retinal vasculitis were included in this study.Patients first consulted the eye clinic and were diagnosed presumed tubercular retinal vasculitis.The patients,seven males and two females,aged from 19 to 66 years,with an average of 43.89 years.The time interval from symptoms to diagnosis ranged from two weeks to six months with an average of 76.27 days.Visual acuity,slit lamp ophthalmoscopy,fundus fluorescein angiography (FFA),optical coherence tomography (OCT),hematological and tuberculosis related investigations were examined and analyzed.All patients had standard anti-tuberculosis treatment.Treatment outcomes were followed for six to 37 months with an average of 14.11 months.Results Baseline visual acuity ranged from hand movement to 0.8 with an average of 0.28.Among 11 eyes,six presented mild to moderate vitritis,five presented as retinal vein occlusion with no obvious vitirits.Fundus examination showed six cases with retinal hemorrhage,four cases with macular edema,two with macular epiretinal membrane,and two with vitreous hemorrhage.FFA revealed 11 cases with leakage of vessels,11 with nonperfusion area,four with macular edema,three with retinal neovascularization,and two with choroidal lesions.OCT of nine eyes suggested six eyes with retinal edema,three with macular edema,three with macular epiretinal membrane.TST of seven patients were all strong positive.T-SPOT.TB of four patients were all positive.Three of eight patients who had chest X-ray or chest CT were suggested tuberculosis infection.Four to six weeks after the start of anti-tuberculosis treatment,vitritis,exudates,retinal and macular edema subsided.During follow up,inflammation was stable with no recurrence observed.The visual acuity of last follow-up ranged from 0.15 to 0.8 with an average of 0.51.Conclusions The main presentations of presumed tubercular retinal vasculitis are vitritis,retinal vein occlusion,and retinal hemorrhage.Standard anti-tuberculosis treatment can improve inflammation and retinal hemorrhage.