نتایج جستجو برای: idiopathic retinal vasculitis

تعداد نتایج: 155576  

Journal: :Klinika oczna 2023

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Świerczyńska M, Sedlak L, Wąs P, Nowak Dorecka Mrukwa-Kominek E. Idiopathic retinal vasculitis, aneurysms and neuroretinitis (IRVAN): a case report outcomes of 1.5-year observation. Klinika Oczna / Acta Ophthalmologica Polonica. 2022. doi:10.5114/ko.2022.118406. APA Świerczyńska, M., Sedlak, L., Wąs, P., Nowak, Do...

2014
Lazha Talat Sue Lightman Oren Tomkins-Netzer

Ischemic retinal vasculitis is an inflammation of retinal blood vessels associated with vascular occlusion and subsequent retinal hypoperfusion. It can cause visual loss secondary to macular ischemia, macular edema, and neovascularization leading to vitreous hemorrhage, fibrovascular proliferation, and tractional retinal detachment. Ischemic retinal vasculitis can be idiopathic or secondary to ...

Journal: :Güncel retina 2023

Idiopathic retinal vasculitis, aneurysm, and neuroretinitis (IRVAN) syndrome, pigmented paravenous chorioretinal atrophy (PPCRA) are rare clinical manifestations of unknown etiology. In recent years, with the widespread use multimodal imaging methods in diseases, information about pathogenesis course these diseases has increased. PPCRA is often detected incidentally asymptomatic, whereas IRVAN,...

Journal: :The British journal of ophthalmology 2005
M J Gallagher K G-J Ooi M Thomas M Gavin

BACKGROUND Antinuclear cytoplasmic antibodies (ANCA) are useful diagnostic serological markers for the most common forms of necrotising vasculitis. ANCA associated vasculitides represent distinctive clinicopathological categories--for example, Wegener's granulomatosis, Churg-Strauss syndrome, microscopic polyangiitis, and idiopathic necrotising crescentic glomerulonephritis, collectively known ...

Journal: :The British journal of ophthalmology 2003
B van Kooij M Canninga van Dijk J de Boer V Sigurdsson A Rothova

AIM To report on eight patients with severe idiopathic intermediate uveitis (IU) and granuloma annulare (GA), a self limiting cutaneous condition of unknown aetiology. METHODS Retrospective case series. Clinical ophthalmic and dermatological data were studied and fluorescein angiography and skin biopsies were reviewed. RESULTS All patients with idiopathic IU had similar ocular features (eig...

2003
B van Kooij M Canninga van Dijk J de Boer V Sigurdsson A Rothova

Aim: To report on eight patients with severe idiopathic intermediate uveitis (IU) and granuloma annulare (GA), a self limiting cutaneous condition of unknown aetiology. Methods: Retrospective case series. Clinical ophthalmic and dermatological data were studied and fluorescein angiography and skin biopsies were reviewed. Results: All patients with idiopathic IU had similar ocular features (eigh...

Journal: :Nepalese journal of ophthalmology : a biannual peer-reviewed academic journal of the Nepal Ophthalmic Society : NEPJOPH 2012
R Kharel Sitaula S Aryal S N Joshi J K Shrestha

OBJECTIVES To study the demographic profile, clinical presentations, management and visual outcome of retinal vasculitis in a tertiary eye care center of Nepal MATERIALS AND METHODS A retrospective, record based study of retinal vasculitis cases in the retina clinic of a tertiary care centre in Nepal from January 2009 to January 2011 was carried out. Results of the study were compared to thos...

Journal: :American Journal of Ophthalmology Case Reports 2016

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید