ABSTRACT
Objective:To observe and analyze the multimodal imaging characteristics of fundus in patients with sympathetic ophthalmia (SO).Methods:A retrospective study. From October 2012 to December 2021, 28 patients (36 eyes) diagnosed SO in the Department of Ophthalmology, Beijing Tongren Hospital were inclued in the study. There were 19 males (25 eyes) and 9 females (11 eyes), with the mean age of 51.61±12.02 years. There were 8 exciting eyes and 28 sympathizing eyes. The time to onset after trauma or surgery was 46.10±107.98 months. All patients underwent examinations including vision test, color fundus photograph, optical coherence tomography (OCT), fundus fluorescence angiography (FFA), indocyanine green angiography (ICGA). Angio-OCT (OCTA) was performed on 3 eyes and fundus autofluorescence (AF) was performed on 8 eyes. The early and late phase were defined respectively as ≤2 months and >2 months. Their multimodal imaging characteristics were summarized.Results:In 8 exciting eyes, subretinal fibrosis with mutifocal retinal atrophy and pigmentation was noted in 5 eyes (62.50%, 5/8), the other 3 eyes showed sunset glow fundus (37.50%, 3/8). In 28 sympathizing eyes, in the early phase, the fundus photograph showed shallow retinal detachment with optic disc edema in 9 eyes (32.14%, 9/28); in the late phase, peripapillary yellowish-white subretinal lesions in 11 eyes (39.29%, 11/28). In the late course of the disease, there were yellow-white lesions around the optic disc (peridisc) and peripheral subretinal area in 11 eyes (39.29%, 11/28). Dalen-Fuchs nodules were found in 10 eyes (35.71%, 10/28). On OCT, multiple serous retinal detachment and irregular choroidal folds were noted in the early phase; hill-like subretinal hyperreflective elevation was noted in peripapillary area and subfovea with presence of cystic spaces in the intraretina in the late phase. FFA examination showed"pinpoint-like" strong fluorescence in the early stage, and "multi-lake-like" fluorescein accumulation and leakage in the late stage; "map-like" weak fluorescence around the disc in the early stage of the disease, dot-like strong fluorescence lesions in each quadrant of the peripheral retina, and fluorescence in the late stage of the disease course. enhanced. ICGA examination showed that the FFA strong fluorescence lesions in the middle and late stages were weak fluorescence. FAF examination, point-like strong and weak autofluorescence lesions with unclear boundaries. Nine sympathizing eyes with subretinal yellow-white lesions has vision without light-0.1 (significantly decreased vison), while 8 eyes with sunset glow fundus was 0.5-1.0 (mildly decreased vison).Conclusions:SO could not only show the semblable features of acute phases of Vogt-Koyanagi-Harada syndrome, but also the yellowish-white lesions in the peripapillary area, macula and periphery. Most of the eyes with peripapillary lesions has a significantly decreased vison, while the eyes with sunset glow fundus has a mildly decreased vison.
ABSTRACT
A síndrome da fibrose sub-retinina é uma doença rara e considerada como parte de um grupo de condições que recebem a denominação de síndrome dos pontos brancos. No entanto, alguns autores a consideram como uma entidade distinta dessas outras doenças com características próprias. Com os casos apresentados, podemos observar muitas dessas características já descritas, como localização e aspecto clínico das lesões, sua evolução e o prognóstico visual final. Seu diagnóstico é muito importante a se considerar em diversos tipos de uveíte, pois o tratamento precoce pode evitar o acometimento bilateral.
The subretinal fibrosis syndrome is a rare disease and is considered part of a group of conditions that are denominated white dots syndrome. However, some authors consider it like a distinct entity from the others diseases with you own features. With these cases we can behold many features already described, like localization and clinical aspect of the lesion, your evolution and the final visual prognosis. It's diagnostic is very important to consider in a varied type of uveitis, because the treatment can avoid the bilateral involvement.
Subject(s)
Adult , Humans , Male , Middle Aged , Disease Progression , Retina/pathology , Uveitis/therapy , Vitreous Body/surgery , Electroretinography , Fibrosis , /immunology , Retinal Detachment , Syndrome , Vitreoretinal SurgeryABSTRACT
A oftalmia simpática é uma panuveíte granulomatosa que se inicia após trauma ocular. O prognóstico é reservado e depende do diagnóstico e tratamento precoces. Os autores descrevem um caso de paciente portador de oftalmia simpática no qual foi realizada tomografia de coerência óptica e instituído tratamento precoce, e sugerem que a tomografia de coerência óptica possa corroborar como exame subsidiário no estudo das características da retina de pacientes portadores dessa doença, especialmente em casos de apresentação rara, com descolamento seroso da retina, como manifestação oftalmológica isolada.
The sympathetic ophthalmia is a granulomatous panuveitis that starts after ocular trauma. The prognosis is poor and depends of both early diagnosis and treatment. The authors describe one case of a patient with sympathetic ophthalmia using optical coherence tomography who was submitted to early treatment, and it suggests that the optical coherence tomography can corroborate as a ancillary method in the study of retina characteristics in sympathetic ophthalmia disease specially in cases of rare presentation, with serous retinal detachment as an isolated ophthalmological manifestation.
Subject(s)
Humans , Male , Young Adult , Ophthalmia, Sympathetic/diagnosis , Tomography, Optical Coherence , Adrenal Cortex Hormones/therapeutic use , Early Diagnosis , Ophthalmia, Sympathetic/drug therapy , Retinal Detachment/diagnosis , Young AdultABSTRACT
This study correlates fluorescein angiography (FA) and indocyanine green angiography (ICGA) to histopathologic findings in a patient with sympathetic ophtalmia. A male with a perforated trauma in right eye presented after two months a decrease in visual acuity of the left eye. FA and ICGA were performed and the images were correlated with the histopathologic findings of the enucleated eye; FA showed background areas of homogeneous hypofluorescence in the arterial and venous phases, as well as areas of granular progressive hyperfluorescence and leakage from the optic disc. ICGA showed areas of hypofluorescence in the early and intermediate phases of the examination, which persisted until the late phase. During the early phase, there was also diffuse hypofluorescence caused by blockage that allowed observation of areas of partial choroidal circulation. The histopathology of the enucleated right eye showed diffuse choriocapillaris edema and inflammation of the choroids, focal areas of hyperplasia of the retinal pigment epithelium (RPE) as well as foci of epithelioid cells located between the choroid and the RPE. Furthermore, lymphocytic infiltration of the episcleral veins and retinal detachment were present. The hyperfluorescence observed on FA was correlated to retinal detachment and optic nerve inflammation. The hypofluorescence noted on FA and ICGA corresponded to the presence of blocking inflammatory cells (Dalen-Fuchs-like nodules) and to diffuse choriocapillaris edema.
O objetivo deste relato de caso foi correlacionar achados da histopatologia com a angiografia por fluoresceína (AF) e por indocianina verde (AIV) em um paciente com oftalmia simpática. Após dois meses de trauma perfurante no olho direito, o paciente apresentou baixa acuidade visual no olho esquerdo (OE). A AF do OE mostrou áreas de hipofluorescência homogênea na fase arterial e venosa, áreas de progressiva hiperfluorescência granular e vazamento do disco. A AIV mostrou áreas de hipofluorescência na fase inicial à tardia. A histopatologia foi realizada após evisceração do olho direito e demonstrou difuso edema da coriocapilar, inflamação da coróide, áreas focais de hiperplasia do epitélio pigmentar da retina, focos de células epitelióides entre a coróide e o epitélio pigmentar da retina, além da infiltração linfocitária das veias episclerais e descolamento de retina. A hiperfluorescência observada na AF foi correlacionada com o descolamento de retina e inflamação do nervo óptico. A hipofluorescência na AF e AIV correspondeu à presença de células inflamatórias (nódulos de Dalen-Fuchs) e edema coriocapilar difuso.