ABSTRACT
We describe a 28-year-old Caucasian female with vigorexy, who had no previous ocular history. She presented with bilateral gradual painless reduction in vision over the past 3 weeks. She had been taking niacin supplements, averaging 500â¯mg daily, for 7 years. Fundus examination revealed bilateral CME, which was confirmed by ocular coherence tomography scan. Fundus fluorescein angiography did not reveal any fluid leakage. Niacin supplementation was discontinued, and after 2 months, the CME had completely resolved, and the best corrected visual acuities improved to 1 in both eyes.
ABSTRACT
To report a unique case of a patient who developed simultaneous bilateral maculopathy presumed from intake of fluoxetine. The optic coherence tomography (OCT) macular showed a subfoveal disruption in the outer retinal layer in both eyes (OU), higher in the left one (OS). Although reported cases of serotonin recapture inhibitors (SSRIs) Maculopathy so far have been caused by sertraline, fluoxetine shares the biological mechanism, and OCT findings and ocular symptoms are the same as published. We should be aware with ocular symptoms in patients that take fluoxetine.
Subject(s)
Fluoxetine , Retinal Diseases , Selective Serotonin Reuptake Inhibitors , Tomography, Optical Coherence , Humans , Fluoxetine/adverse effects , Selective Serotonin Reuptake Inhibitors/adverse effects , Retinal Diseases/chemically induced , Retinal Diseases/diagnostic imaging , Female , Male , Middle AgedABSTRACT
ABSTRACT A 42-year-old female patient had vision loss and chronic epiphora in her left eye. Her best-corrected visual acuity was 10/10 in the right eye and 0.3/10 in the left eye. The anterior segment examination results were normal. In fundus examination, choroidal folds were detected. Optical coherence tomography showed elevation on the macula and choroidal folds. Ultrasonography revealed a T-sign. Magnetic resonance imaging revealed an ethmoidal mucocele that compresses the orbital tissues. Surgical treatment was performed in the otorhinolaryngology department. Postoperatively, choroidal folds recovered, and the best-corrected visual acuity improved, but subretinal fluid accumulated. During the follow-up period without any treatment, subretinal fluid totally disappeared.
RESUMO Paciente do sexo feminino, 42 anos, com perda visual e epífora crônica no olho esquerdo. Sua acuidade visual melhor corrigida foi de 10/10 no olho direito e 0,3/10 no olho esquerdo. O exame do segmento anterior foi normal. No exame de fundo de olho, foram detectadas pregas coroidais. A tomografia de coerência óptica revelou elevação na mácula e pregas coroidais. A ultrassonografia revelou sinal T. A imagem de ressonância magnética mostrou mucocele etmoidal que comprime os tecidos orbitários. O Departamento de Otorrinolaringologia realizou o tratamento cirúrgico. No pós-operatório, as dobras coroidais se recuperaram, a acuidade visual melhor corrigida foi melhorada, mas ocorreu líquido sub-retiniano. Durante o período de acompanhamento sem qualquer tratamento, o líquido sub-retiniano recuperou-se totalmente.
ABSTRACT
ABSTRACT Maculopathy from prolonged exposure to solar light is a rare but well-recognized clinical entity of vision loss and macular damage. Photochemical damage precedes visual decline, and in mild cases, vision usually returns fully or partially. With the advancement of humanity, other forms of macular injuries induced by light radiation have emerged, increasing the group of photic maculopathies. In this report, we describe the cases of five patients where a diagnosis of photic maculopathy was made based on the anamnesis, clinical findings, and complementary exams. We compare the five cases regarding their similarities and differences, as well as review the literature on the subject.
RESUMO A maculopatia causada pela exposição prolongada à luz solar é uma entidade clínica rara, mas bem reconhecida, de perda de visão e dano macular. O dano fotoquímico precede o declínio visual e em casos leves a visão geralmente retorna total ou parcialmente. Com o avanço da humanidade, surgiram outras formas de lesões maculares induzidas pela radiação luminosa, aumentando o grupo das maculopatias fóticas. Neste relato, descrevemos os casos de cinco pacientes onde o diagnóstico de maculopatia fótica foi feito com base na anamnese, achados clínicos e exames complementares. Comparamos os quatro casos quanto às suas semelhanças e diferenças, bem como revisamos a literatura sobre o assunto.
ABSTRACT
La neurorretinopatía macular aguda es una condición rara con patogenia microvascular. Se presenta con un inicio agudo con escotomas paracentrales correspondientes a lesiones paramaculares evidentes. Los avances en las imágenes multimodales permitieron caracterizar este trastorno de retina y crear nuevos conceptos. Serraf, en el 2013, identificó dos formas por medio de la tomografía de coherencia óptica dominio espectral: el tipo 1 conocido como maculopatía paracentral aguda media en la cual se observa una banda hiperreflectiva en la capa nuclear interna, y el tipo 2 en el cual la banda hiperreflectiva se ubica en la capa nuclear externa, que involucra la zona elipsoide y la zona de interdigitación con el epitelio pigmentario de la retina. Hasta el momento no existe cura; pero se puede actuar sobre los factores de riesgo. Por ser una condición rara y por no existir reportes hasta el momento en Cuba es que se presentan a continuación dos pacientes con cuadros clínicos similares de estas dos variantes; concluyendo la importancia que presentan las imágenes multimodales como medio auxiliar diagnóstico(AU)
Acute macular neuroretinopathy is a rare condition with complex pathogenesis and microvascular cause. It appears with acute onset, with paracentral scotomas corresponding to obvious paramacular lesions. Advances in multimodal imaging made it possible to characterize this retinal disorder and to create new concepts. Serraf, in 2013, identified two forms by spectral domain optical coherence tomography: type 1, known as paracentral acute middle maculopathy, in which a hyperreflective band is observed in the inner nuclear layer; and type 2, in which the hyperreflective band is located in the outer nuclear layer, involving the ellipsoid zone and the zone of interdigitation with the retinal pigment epithelium. Up to this moment, there is no cure; but it is possible to act on the risk factors. Because it is a rare condition and because there are no reports so far in Cuba, two patients with similar clinical pictures of these two variants are presented; concluding the importance of multimodal images as an auxiliary diagnostic tool(AU)
Subject(s)
Humans , White Dot Syndromes/pathologyABSTRACT
La maculopatía por inmunoganmapatía es una enfermedad macular inusual caracterizada por la presencia de fluido intra y subretinal en asociación con ganmapatías monoclonales. Puede constituir la primera manifestación de enfermedad sistémica en un número considerable de pacientes. La infiltración de la retina neurosensorial y del espacio subretiniano por las inmunoglobulinas provoca un aumento de la presión osmótica lo cual genera acumulación del fluido intra y subretinal. El "silencio angiográfico" la distingue de otras maculopatías con desprendimientos serosos. La plasmaféresis combinada con quimioterapia constituye la primera línea del tratamiento. Aunque el líquido intrarretinal mejora considerablemente, el subretinal persiste en la mayoría de los ojos. La agudeza visual mejor corregida final muestra una ganancia de 0,3 décimas como promedio después del tratamiento. Con el objetivo de exponer contenido actualizado sobre maculopatía por inmunoganmapatía, se realizó una revisión de las publicaciones más relevantes relacionadas con el tema durante los últimos ocho años(AU)
Immunoganmapathy maculopathy is an unusual macular disease characterized by the presence of intra- and subretinal fluid in association with monoclonal ganmapathies. It may constitute the first manifestation of systemic disease in a considerable number of patients. Infiltration of the neurosensory retina and the subretinal space by immunoglobulins causes an increase in osmotic pressure which leads to accumulation of intra- and subretinal fluid. The "angiographic silence" distinguishes it from other maculopathies with serous detachment. Plasmapheresis combined with chemotherapy is the first line of treatment. Although intraretinal fluid improves considerably, subretinal fluid persists in most eyes. The final best-corrected visual acuity shows a gain of 0.3 tenths on average after treatment. In order to expose updated content on immunoganmopathy maculopathy, a review of the most relevant publications related to the subject during the last eight years was performed(AU)
Subject(s)
Humans , Female , Drug Therapy/methods , Macular Degeneration/diagnostic imagingABSTRACT
A cyclodialysis cleft is a rare disease that is produced as a result of a separation of the longitudinal fibers of the ciliary body muscle from the scleral spur. A stepwise approach is the best course of action to treat cyclodialysis, starting with medical therapy and continuing with more invasive surgical options. We report a case of ocular hypotony due a traumatic cyclodialysis successfully resolved with transscleral cryotherapy.
Subject(s)
Cyclodialysis Clefts , Eye Injuries , Ocular Hypotension , Ciliary Body/surgery , Cryotherapy , Eye Injuries/complications , Eye Injuries/surgery , Humans , Ocular Hypotension/etiology , Ocular Hypotension/surgeryABSTRACT
La hendidura de ciclodiálisis es una enfermedad rara que se produce como resultado de una separación de las fibras longitudinales del músculo del cuerpo ciliar del espolón escleral. La mejor forma de tratar la ciclodiálisis es por etapas, comenzando con una terapia médica y continuando con opciones quirúrgicas más invasivas. Presentamos un caso de hipotonía ocular debida a una ciclodiálisis traumática que se resolvió con éxito mediante crioterapia transescleral (AU)
A cyclodialysis cleft is a rare disease that is produced as a result of a separation of the longitudinal fibers of the ciliary body muscle from the scleral spur. A stepwise approach is the best course of action to treat cyclodialysis, starting with medical therapy and continuing with more invasive surgical options. We report a case of ocular hypotony due a traumatic cyclodialysis successfully resolved with transscleral cryotherapy (AU)
Subject(s)
Humans , Female , Aged , Cryotherapy/methods , Choroid Diseases/etiology , Choroid Diseases/therapy , Treatment Outcome , Rare Diseases , Ocular HypotensionABSTRACT
ABSTRACT The thermal effects of laser cutting machines could damage the macula. A few studies in the literature have described macular injury induced by industrial laser burns. The aim of this study was to report the clinical, visual, and optical coherence tomography findings in a gold refinery worker with laser-induced maculopathy. A 21-year-old male gold refinery worker had vision loss in his right eye after using a laser cutting machine without wearing laser eye protection gear. At the first visit (24 h later), his best-corrected visual acuity was 7/10 in the right eye and 10/10 in the left eye. The anterior segment examination was normal. In fundus examination, focal, round, and yellowish lesion was detected within the fovea. The optical coherence tomography findings were foveal outer retinal disruptions and irregularities extending from the outer plexiform layer to the retina pigment epithelium. After 4 months, the best-corrected visual acuity had improved to 1.0, and the optical coherence tomography findings had resolved.
RESUMO Os efeitos térmicos das máquinas de corte a laser podem danificar a mácula. Poucos estudos na literatura tem descrito a lesão macular por queimadura a laser industrial. Neste estudo, objetivamos relatar os achados clínicos, visuais e de tomografia de coerência óptica em um trabalhador de refinaria de ouro com maculopatia induzida por laser. O trabalhador da refinaria de ouro de 21 anos teve perda de visão no olho direito depois de usar uma máquina de corte a laser sem usar equipamento protetor ocular para laser. Sua acuidade visual melhor corrigida foi de 7/10 no olho direito e 10/10 no olho esquerdo na primeira consulta (24h depois). O exame do segmento anterior estava normal. No exame de fundo de olho, lesões focais, redondas e amareladas foram detectadas dentro da fóvea. Os achados da tomografia de coerência óptica revelaram rupturas na fóvea da retina externa e irregularidades estendendo-se da camada plexiforme externa ao epitélio pigmentar da retina. Após 4 meses, a acuidade visual melhor corrigida melhorou para 1,0 e os achados da tomografia de coerência óptica foram revigorados.
ABSTRACT
Caso clínico Varón de 58 años que acude derivado a consultas de sección retina por pérdida de agudeza visual (AV) en el ojo izquierdo (OI). En la primera visita, la AV fue de 0,9 en el ojo derecho (OD) y movimiento de manos en OI y la presión intraocular (PIO) fue de 34 mmHg y 42 mmHg en ojo derecho e izquierdo, respectivamente. En la fundoscopia se observó aumento de la excavación del nervio óptico y palidez papilar en ambos ojos y edema del polo posterior en OI. La tomografía de coherencia óptica (OCT) y la angiografía fluoresceínica confirmaron el diagnóstico de desprendimiento de retina (DR) seroso macular causado por foseta papilar secundaria a glaucoma. El tratamiento quirúrgico combinado mediante implante de dispositivo de drenaje ExPress, vitrectomía pars plana (VPP) y endofotocoagulación láser yuxtapapilar logró la normalización de la PIO y la resolución anatómica completa del DR macular (AU)
Case report A 58-year-old man was referred to the retina specialist for evaluation of decreased vision in the left eye (LE). At the first visit, visual acuity was 0.9 in right eye (RE) and hands movement in LE, and the intraocular pressure (IOP) was 34 mmHg and 42 mmHg in right and left eye, respectively. Dilated funduscopic examination revealed papillary pallor, increased cup-to-disc ratio of the optic nerve in both eyes, and retinal posterior pole edema in the LE. Optical coherence tomography (OCT) and fluorescein angiography assessment confirmed the diagnosis of a macular serous retinal detachment (RD) caused by an optic disc pit secondary to glaucoma. Combined surgical treatment with ExPress drainage device implantation, pars plana vitrectomy (PPV), and juxtapapillar laser endophotocoagulation was performed. IOP normalization was achieved as well as complete anatomical resolution of macular RD (AU)
Subject(s)
Humans , Male , Middle Aged , Glaucoma/complications , Macular Degeneration/etiology , Macular Degeneration/surgery , Combined Modality Therapy , Filtering Surgery , Vitrectomy , Laser Coagulation , Treatment OutcomeABSTRACT
CASE REPORT: A 58-year-old man was referred to the retina specialist for evaluation of decreased vision in the left eye (LE). At the first visit, visual acuity was 0.9 in right eye (RE) and hands movement in LE, and the intraocular pressure (IOP) was 34â¯mmHg and 42â¯mmHg in right and left eye, respectively. Dilated funduscopic examination revealed papillary pallor, increased cup-to-disc ratio of the optic nerve in both eyes, and retinal posterior pole oedema in the LE. Optical coherence tomography (OCT) and fluorescein angiography assessment confirmed the diagnosis of a macular serous retinal detachment (RD) caused by an optic disc pit secondary to glaucoma. Combined surgical treatment with ExPress drainage device implantation, pars plana vitrectomy (PPV), and juxtapapillar laser endophotocoagulation was performed. The IOP returned to normal, as well as complete anatomical resolution of macular RD.
Subject(s)
Eye Abnormalities , Glaucoma , Macular Degeneration , Optic Disk , Glaucoma/etiology , Humans , Male , Middle Aged , Retrospective StudiesABSTRACT
A case of solar maculopathy is described in a 36-year-old man with a history of bipolar disorder. The patient reported directly looking at the sun for several hours in the setting of a bipolar disorder decompensation. The visual acuity was 0.3 in both eyes (BE). Intraocular pressure and anterior segment were normal. In the fundus exam, a peri-macular halo with loss of the foveolar reflex was observed in BE. The macular optical coherence tomography revealed a disruption of the ellipsoid line and the retinal pigment epithelium. Bilateral central defects were seen in the Humphrey 24-2 visual field. After 6 months of follow-up, the visual clinical picture remains stable with the same degree of visual acuity. Solar maculopathy is a disorder due to the phototoxic effects of radiation, which cause a decrease in visual acuity by disrupting the retinal photoreceptor layer.
Subject(s)
Bipolar Disorder , Macular Degeneration , Retinal Diseases , Adult , Humans , Male , Retinal Diseases/diagnosis , Tomography, Optical Coherence , Visual AcuityABSTRACT
Se describe el caso clínico de un varón de 36 años, con antecedentes de trastorno bipolar, que fue diagnosticado de maculopatía solar en ambos ojos (AO). El paciente refería visión directa del sol, mantenida y en múltiples ocasiones, coincidiendo con descompensación del trastorno bipolar. En la exploración oftalmológica completa presentaba una agudeza visual de 0,3 en AO, con presión intraocular y biomicroscopia normales. En el fondo de ojo se objetivó un halo perimacular con pérdida del reflejo foveolar en AO. En la tomografía de coherencia óptica macular se halló una disrupción de la línea de elipsoides y del epitelio pigmentario de la retina de AO y en la campimetría visual defectos centrales en AO. Tras 6 meses de seguimiento, la clínica visual continúa estable con el mismo grado de agudeza visual. La maculopatía solar es una afectación debida a los efectos fototóxicos de la radiación por exposición directa al sol que cursa con disminución de la agudeza visual, siendo característica en la tomografía de coherencia óptica la disrupción en la capa de fotorreceptores (AU)
A case of solar maculopathy is described in a 36-year-old man with a history of bipolar disorder. The patient reported directly looking at the sun for several hours in the setting of a bipolar disorder decompensation. The visual acuity was 0.3 in both eyes (BE). Intraocular pressure and anterior segment were normal. In the fundus exam, a peri-macular halo with loss of the foveolar reflex was observed in BE. The macular optical coherence tomography revealed a disruption of the ellipsoid line and the retinal pigment epithelium. Bilateral central defects were seen in the Humphrey 24-2 visual field. After 6 months of follow-up, the visual clinical picture remains stable with the same degree of visual acuity. Solar maculopathy is a disorder due to the phototoxic effects of radiation, which cause a decrease in visual acuity by disrupting the retinal photoreceptor layer (AU)
Subject(s)
Humans , Male , Adult , Bipolar Disorder , Macular Degeneration/etiology , Retinal Diseases/etiology , Sunlight/adverse effects , Tomography, Optical Coherence , Visual AcuityABSTRACT
Presentamos 2 casos de maculopatía idiopática aguda unilateral en 2adultos jóvenes, un varón de 24 años y una mujer de 37 años. Ambos sufrieron una pérdida aguda de visión acompañada de manifestaciones clínicas compatibles con la maculopatía idiopática unilateral aguda. Como hallazgo excepcional, presentaron lesiones multifocales alrededor de una lesión central de mayor tamaño. Con el tiempo, se produjo la recuperación espontánea de la pérdida visual. La maculopatía idiopática aguda unilateral puede presentarse de formas distintas de la convencional, por lo que deberíamos considerar la posibilidad de encontrarnos ante estas formas atípicas (AU)
Two cases of multifocal unilateral acute idiopathic maculopathy are presented, one in a 24 year-old man, and another in a 37 year-old woman. Both of them presented with acute vision loss and clinical findings compatible with unilateral acute idiopathic maculopathy. As a relatively uncommon finding, they had multifocal lesions around a larger central lesion. They experienced a spontaneous improvement of their vision. Atypical presentations of unilateral acute idiopathic maculopathy like multifocal lesions are possible. Ophthalmologists should be aware of this rare form of presentation (AU)
Subject(s)
Humans , Male , Female , Adult , Macular Degeneration/diagnostic imaging , Macular Degeneration/drug therapy , Tomography, Optical Coherence , Fluorescein Angiography , Acute DiseaseABSTRACT
RESUMEN Se reportó el caso de un paciente con maculopatía en ojo de buey, asociada al uso de cloroquina. El uso de cloroquina en patologías reumatológicas puede provocar daño retinal relacionado con la dosis y el tiempo de evolución del tratamiento. Puede provocar desde afectación visual leve hasta daño irreversible de la visión, lo que depende del tiempo en que se realice el diagnóstico. Se presentó una paciente de 72 años, con diagnóstico de artritis reumatoide desde hace 21 años y tratamiento con cloroquina desde hace 15. Acudió a consulta con disminución de la visión lenta y progresiva bilateral. En el examen oftalmológico de fondo de ojo se diagnosticó maculopatía en ojo de buey. Este diagnóstico se confirmó por estudios de autofluorescencia y por la tomografía de coherencia óptica (AU).
ABSTRACT A case is reported of a patient with maculopathy in bulls' eye associated to the use of chloroquine. The use of chloroquine associated with rheumatologic diseases can cause retinal damage related to the dose and the time of treatment evolution. It can cause from mild visual impairment to irreversible vision damage depending on the time the diagnosis is made. A 72-year-old female patient is presented with a diagnosis of rheumatoid arthritis for 21 years and treatment with chloroquine for 15 years. She assisted the consultation with a slow and progressive bilateral vision decrease; at the ophthalmological examination of the fundus a maculopathy in bull's eye was diagnosed, later confirmed by auto fluorescence and optical coherence tomography studies (AU).
Subject(s)
Humans , Female , Aged , Adonis/drug effects , Macular Degeneration/diagnosis , Blindness/chemically induced , Adonis/toxicity , Macular Degeneration/complications , Macular Degeneration/pathologyABSTRACT
A cyclodialysis cleft is a rare disease that is produced as a result of a separation of the longitudinal fibers of the ciliary body muscle from the scleral spur. A stepwise approach is the best course of action to treat cyclodialysis, starting with medical therapy and continuing with more invasive surgical options. We report a case of ocular hypotony due a traumatic cyclodialysis successfully resolved with transscleral cryotherapy.
ABSTRACT
CASE REPORT: A 58-year-old man was referred to the retina specialist for evaluation of decreased vision in the left eye (LE). At the first visit, visual acuity was 0.9 in right eye (RE) and hands movement in LE, and the intraocular pressure (IOP) was 34 mmHg and 42 mmHg in right and left eye, respectively. Dilated funduscopic examination revealed papillary pallor, increased cup-to-disc ratio of the optic nerve in both eyes, and retinal posterior pole edema in the LE. Optical coherence tomography (OCT) and fluorescein angiography assessment confirmed the diagnosis of a macular serous retinal detachment (RD) caused by an optic disc pit secondary to glaucoma. Combined surgical treatment with ExPress drainage device implantation, pars plana vitrectomy (PPV), and juxtapapillar laser endophotocoagulation was performed. IOP normalization was achieved as well as complete anatomical resolution of macular RD.
ABSTRACT
OBJECTIVE: To study the differences between solar retinopathy (SR) and the maculopathy produced by laser pointer (LPM) using multimodal imaging. METHOD: A retrospective series is presented of 20 eyes of 12 patients with injuries associated with light, 7 with SR-compatible injuries, and 5 with LPM. At diagnosis, a complete ophthalmological examination was performed, including visual acuity (VA), retinography, and spectral domain optical coherence tomography (OCT). The patients were followed-up for a mean period of 20 months. RESULTS: LPM is common in paediatrics (mean age 15.60±1.5years), and SR affects patients of all ages (mean age 47.56±1.51years). VA at diagnosis in LPM is greater, and recovery is more complete than in solar retinopathy. In conventional retinography, SR is shown as a single lesion in the macular area (100% of cases), while LPM usually presents as multifocal lesions (86% of cases). Infrared reflectance makes this difference clearer. The main sign in OCT is the disruption of the ellipsoid layer and interdigitation zone. This sign is maintained over time, and its size is greater in the SR than in the LPM. Hyper-reflective columns and hyper-reflective reaction of the retinal pigment epithelium are associated with the acute phase. CONCLUSIONS: LPM and SR show significant differences in the type of patient affected, as well as in the signs in multimodal imaging, as well as in functional impairment and their evolution.
ABSTRACT
Two cases of multifocal unilateral acute idiopathic maculopathy are presented, one in a 24 year-old man, and another in a 37 year-old woman. Both of them presented with acute vision loss and clinical findings compatible with unilateral acute idiopathic maculopathy. As a relatively uncommon finding, they had multifocal lesions around a larger central lesion. They experienced a spontaneous improvement of their vision. Atypical presentations of unilateral acute idiopathic maculopathy like multifocal lesions are possible. Ophthalmologists should be aware of this rare form of presentation.
ABSTRACT
RESUMEN Presentamos el caso de un paciente con foseta del disco óptico, quien presentó una disminución de la agudeza visual secundaria a desprendimiento seroso de retina. Se decidió realizar una inyección intravítrea de 0.3ml de gas C3F8 (100%), seguida de fotocoagulación con láser de argón en el borde temporal de la foseta, logrando reaplicación total de la retina, con reabsorción de todo el líquido subretiniano visible en la tomografía de coherencia optica (OCT) luego de 400 días. Además hubo una mejoría significativa en la agudeza visual.
ABSTRACT We present the case of a patient with an optic disk pit, presenting with great loss of visual acuity secondary to serous retinal detachment. The management chosen was an intravitreal injection of 0.3 mL of C3F8 (100%), followed by argon laser photocoagulation on the temporal edge of the pit, ), achieving total retinal reattachment , and reabsorption of all subretinal fluid visible at optical coherence tomography after 400 days, in addition to great improvement in visual acuity.
