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2021, Ophthalmology Research: An International Journal
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5 pages
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Aims: To describe a solar retinopathy. Presentation of Case: ALPN, 29 years old, male, with cognitive deficit that started after a car accident that occurred at the age of 6 years, attends the ophthalmology clinic of the University Hospital Antônio Pedro, Rio de Janeiro, Brazil with complaints of decreased visual acuity and metamorphopsia in both eyes (AO) started approximately 8 months ago. Family members reported that after the accident, the patient had the habit of spending mornings and afternoons looking at the sun. Discussion: Solar retinopathy is caused by the photochemical and thermal effects of ultraviolet radiation on retinal cells, especially in the outer retina and retinal pigment epithelium (RPE). Symptoms can start a few hours after direct observation of the sun, and in most cases a bilateral involvement, although asymmetrically with variable visual acuity. Conclusions: A Solar retinopathy has a multifactorial origin, as it is related to the exposure time and the suscep...
Arquivos Brasileiros de Oftalmologia, 2013
Relato de Caso | Case RepoRt INTRODUCTION Solar retinopathy, also known as photomaculopathy, eclipse re tinopathy and foveomacular retinitis, is retinal damage resulting from direct or indirect solar observations during a solar eclipse or on a normal day (1). Light can damage the retina via mechanical, thermal or photochemical means, either alone or in combination. Photoche mical damage (actinic) occurs during prolonged low irradiance ex posure that lasts more than 10 seconds (2). Retinal impairment can be mild or severe (3). Young people are most vulnerable to damage (3). The earliest definitive report was in the eighteenth century and involved five cases of maculopathy due to exposure to the sun, fire or snow (4). The objective of the present study is to report the case of a patient suffering from solar retinopathy and to discuss its disease etiology and prevention. CASE REPORT A.M.R.B., 38, female, white, married, complained of metamor phopsia in the left eye for five months. The patient denied using me dication regularly, having any systemic diseases or having a history of abnormal solar exposure. Upon physical examination, the patient had 20/20 visual acuity in both eyes, including 4.75 sph. 0.50 cyl. at 20° in the right eye (RE) and 5.25 sph. in the left eye (LE). Biomicroscopy showed no changes
Delhi Journal of Ophthalmology, 2013
Solar observa on and eye damage is known for centuries. Unprotected eclipse viewing is the leading cause of solar re nopathy. Inspite of using commercially available cer fi ed solar fi lters, use of binoculars, exposed photographic fi lm and X-ray fi lm are common unsafe prac ce of eclipse viewing. Public awareness by media campaigns about the appropriate protec ve measures while viewing an eclipse is the mainstay in the preven on of this disease. The natural course of solar re nopathy is to show resolu on and visual improvement, but use of an-infl ammatory drugs hastens the recovery. We report a case of young male with acute solar re nopathy a er viewing solar eclipse. The pa ent was successfully treated with cor costeroids with complete visual rehabilita on.
Transactions of the American Ophthalmological Society, 1987
A 20-vear-old white woman who sunbathed in Ann Arbor, 'Michigan for 2 hours on March 28, 1986 noted the onset of a central scotoma in each eye 1 day later. The patient denied anv direct sun gazing, the use of stunglasses, the wearing of a hat, the use of systemic or topical drugs, and a previous ocular or medical history. The patient also experienced a severe sunburn on the day of sun exposure. An examination by a local retinal specialist on April 2, 1986 revealed a visual acuity of 20/80 OD and 20/40 OS. A relative central scotoma and metamorphopsia were noted bilaterally on Amsler grid testing. The anterior slit-lamp examination was normal in each eye. The fundus examination revealed a yellowish-gray disturbance in the foveal area of each eye, more prominent in the right eye, which was her dominant one. Some greyish discoloration to the pigment epithelium was evident surrounding the more conspicuous vellowish lesions. The patient was examined in New York City on July 21, 1986, approximately 3 months later. At that time, the visual acuity had improved to 20/25 OD and 20/20 OS. The patient still described bilateral, relative scotomas and metamorphopsia. The yellowish-gray reaction in the macuila was now replaced by a juxtafoveal cyst in each eye. The reddish, irregular, but well demarcated cystic thinning of the outer retina measured 50 ,u OD and 25 p. OS. There was no associated exudative manifestation in the macula of either eye. A fluorescein angiogram revealed a minimal degree of retinal pigment epithelial "window defect" at the site of the cystic disturbanice in the right eye. The patient was a bilateral emmetrope. CASE 2 A 27-year-old white male medical student who sunbathed and exercised for 3 hours on March 29, 1986 in Teaneck, New Jersey, developed blurred vision in the right eye on March 30, 1986. There was also a slight but poorly characterized disturbance in the central vision of the left eye. The patient denied any direct sun gazing, the use of sunglasses, the wearing of a hat, the use of systemic or topical drugs, and a previous ocular or medical history. He also sustained a slight sunburn, which was unusual for this olive-skinned individual. An examination on April 9, 1986 revealed a visual acuity of 20/40 OD with eccentric fixation and 20/20 OS. A relative central scotoma with metamorphopsia was described in the right eye and a faint degree ofjuxtafoveal relative scotoma was noted in the left eye on Amsler grid testing. The anterior slit-lamp examination was normal in each eye. Biomicroscopic examination of the fundus with the Goldmann lens revealed a very faintly evident reddish juxtafoveal cyst in the right eye. There was also a perifoveal granular appearance to the retinal pigment epithelium in that eye. An indistinct appearance to the perifoveal region of the left eye was noted. A fluorescein angiogram was normal bilaterally. A follow-up examination on June 16, 1986 revealed a visual acuity of 20/20 OU with a persistence of a small relative scotoma and metamorphopsia OD, but no evident visual defect OS. The cystic macular lesion in the right eye was now clearly evident, but the perifoveal retinal pigment
Case Reports in Ophthalmological Medicine, 2013
Purpose. Solar retinopathy is a rare clinical disturbance, for which spectral-domain optical coherence tomography (SD-OCT) findings are not always consistent. We report on two cases of solar retinopathy and discuss its differential diagnosis. Methods. This is an observational case study. Results. A 12-year-old female was referred to ophthalmology for bilateral scotoma. Visual acuity was 20/50 in both eyes. Fundus examination was unremarkable, except for slight yellowish material in the central macula, bilaterally. SD-OCT revealed juxtafoveal microcystic cavities in the outer retina, interruption of the external limiting membrane and the inner and outer segment junctions, with disorganized material in the vitelliform space. Fundus autofluorescence showed hypoautofluorescence surrounded by a relatively hyperautofluorescent ring, bilaterally. Similar clinical and morphological findings were detected in a 27-year-old male. Conclusions. Solar retinopathy has a subtle presentation and patients often deny sun-gazing. SD-OCT and fundus autofluorescence are noninvasive and useful tools for its diagnosis.
Nigerian Journal of Medicine, 2020
IntroductIon Solar maculopathy (also known as photic retinopathy, foveomacular retinitis, solar retinitis, and eclipse retinopathy) refers to photochemical toxicity and resultant injury to retinal tissues, usually occurring at the fovea. [1] The longer wavelength end of ultraviolet-A (365-440 nm), visible (400-700 nm), and near infrared (IR) (IRA, 700-1400 nm) light not absorbed by the cornea, lens, and aqueous humour pass through the ocular media, converge on the retina and are absorbed by the photoreceptors and lipofuscin-containing retinal pigment epithelium (RPE) causing damage. [2] They exert their effects on the retina, especially the macula. Histopathological studies have confirmed that the primary lesion occurs in the RPE layer with subsequent photoreceptor damage. [2]
Indian Journal of Ophthalmology, 2016
Medicine & Health
Solar retinopathi merupakan satu penyakit retina yang disebabkan oleh pandangan terhadap cahaya matahari. Diagnosis penyakit ini amat mencabar dan memerlukan sejarah kesihatan dan penyiasatan yang teliti. Laporan kes ini adalah berkenaan seorang pemetik buah-buahan yang berumur 55 tahun yang mengalami kehilangan penglihatan kekal di bahagian tengah medan penglihatan. Diagnosis solar retinopathi telah dibuat berdasarkan kepada sejarah yang diberi oleh pesakit berkenaan, bersama penyiasatan menggunakan pengimejan seperti optical coherence tomography (OCT), infra merah (IF) dan fundus autofluorescence (FAF) yang memainkan peranan penting dalam kes ini. Kesimpulannya, solar retinopathi adalah satu penyakit yang sukar untuk dipulihkan. Penyiasatan dengan cara pengimejan memainkan peranan yang penting untuk merangkul diagnosis yang betul. Justeru itu, pemakaian cermin mata hitam adalah disarankan untuk semua pesakit yang sering terdedah kepada cahaya matahari.
Collegium antropologicum, 2007
A clinical epidemiological study has been conducted as apart of research project investigating chronic exposure to solar ultraviolet radiation (UVR) as a factor contributing to the onset of age-related macular degeneration (ARMD). The study included 623 subjects older than 50 from two different geographic areas, one with high solar radiation (the island of Solta - Region 1) and the other (Zagreb and its surroundings - Region 2) with low solar radiation. Individual exposure to UVR was assessed according to global exposure to sunlight, on the basis detailed history of life-long exposure to sunlight, with special reference to professional history and geophysical specificities of the respective areas. Different grades of ARMD were based on the fundus photographs and flourescein angiography. Statistically significant relation was found between ARMD and mean daily exposure (in hours) to solar radiation in Region 1 (chi2 = 186.22; p = 0.000), Region 2 (chi2 = 25.66; p = 0.000) and in both ...
Espacio Abierto Cuaderno Venezolano de Sociología, 2018
El objetivo de este trabajo es abordar, en clave socio-histórica y política, el devenir de las organizaciones piqueteras en Argentina del siglo XXI, prestando especial atención a las articulaciones con el contexto que las circunda. En ese sentido, se consideran no sólo las relaciones con los gobiernos y las políticas que éste implementa – las acuales pueden favorecer u obstaculizar el accionar colectivo-; sino también las modificaciones que la organización popular puede introducir sobre aquellas condiciones que se creen injustas o insostenibles. El análisis se centra tanto en los orígenes de este movimiento social amplio y heterogéneo, como también en sus reconfiguraciones durante el Kirchnerismo, y especialmente, en relación al macrismo. Antes que aseveraciones cerradas, se intenta pensar en los cambios y desafíos operados en los últimos años.
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