Diffuse unilateral subacute neuroretinitis in South Korea: a case report

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Diffuse unilateral subacute neuroretinitis.

The clinical syndrome of diffuse unilateral subacute neuroretinopathy (DUSN) has been characterised in its early and late stages. Different types of migrating worms in the subretinal and intraretinal space have been described as the cause of the clinical syndrome. We observed a patient with a long history of visual loss, vitritis, and a fundus of abnormal appearance where the worm was noted to ...

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Diffuse Unilateral Subacute Neuroretinitis in a Healthy Korean Male: The First Case Report in Korea

A 52-yr-old male was referred for progressive visual loss in the left eye. The decimal best-corrected visual acuity (BCVA) was 0.01. Fundus examination revealed diffuse retinal pigment epithelial degeneration, focal yellow-white, infiltrative subretinal lesion with fuzzy border and a live nematode within the retina. Diffuse unilateral subacute neuroretinitis (DUSN) was diagnosed and the direct ...

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Intraocular nematode with diffuse unilateral subacute neuroretinitis: case report

BACKGROUND Live intraocular nematode is a rare occurrence. Nematode can migrate actively within the eye, creating visual symptoms and damaging ocular tissue. CASE PRESENTATION A 26-year old man presented with painless reduced vision of the left eye for one week duration. It was associated with floaters. Visual acuity on the left eye was hand movement. Anterior segment examination was normal w...

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[Diffuse unilateral subacute neuroretinitis (DUSN): current update].

Diffuse unilateral subacute neuroretinitis (DUSN) is a form of uveitis that can potentially lead to blindness. In Brazil and other parts of South America, diffuse unilateral subacute neuroretinitis is an important cause of posterior uveitis in children and healthy young adults. If diagnosed and treated in early stage, allows a resolution of symptoms with improvement of visual acuity. If the dis...

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ژورنال

عنوان ژورنال: Acta Ophthalmologica

سال: 2019

ISSN: 1755-375X,1755-3768

DOI: 10.1111/j.1755-3768.2019.5096