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1.
Gac. méd. Méx ; Gac. méd. Méx;155(5): 458-462, Sep.-Oct. 2019. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1286543

RESUMEN

Introduction: Patients with diabetic macular edema can develop fundus autofluorescence alterations; thus far, these alterations have been more widely studied with scanning or confocal laser systems. Objective: To describe and classify fundus autofluorescence abnormal patterns in patients with diabetic macular edema using the fundus autofluorescence system with a flash camera. Method: Observational, retrospective, cross-sectional, descriptive study. Fundus autofluorescence digital images of non-comparative cases with untreated diabetic macular edema, obtained and stored with a flash camera system, were assessed. Inter-observer variability was evaluated. Results: 37 eyes of 20 patients were included. Lens opacity was the most common cause of inadequate image quality. Five different fundus autofluorescence patterns were observed: decreased (13%), normal (40%), single-spot hyper-autofluorescent (17 %), multiple-spot hyper-autofluorescent (22 %) and plaque-like hyper-autofluorescent (8 %). The kappa coefficient was 0.906 (p = 0.000). Conclusions: Different fundus autofluorescence phenotypic patterns are observed with flash camera systems in patients with diabetic macular edema. A more accurate phenotypic classification could help establish prognostic factors for visual loss or for the design of clinical trials for diabetic macular edema.


Asunto(s)
Humanos , Masculino , Femenino , Persona de Mediana Edad , Edema Macular/diagnóstico por imagen , Retinopatía Diabética/diagnóstico por imagen , Imagen Óptica/instrumentación , Imagen Óptica/métodos , Fenotipo , Variaciones Dependientes del Observador , Edema Macular/clasificación , Edema Macular/etiología , Estudios Transversales , Estudios Retrospectivos , Diabetes Mellitus Tipo 2/complicaciones , Retinopatía Diabética/clasificación , Retinopatía Diabética/complicaciones , México
2.
Am J Case Rep ; 20: 300-305, 2019 Mar 07.
Artículo en Inglés | MEDLINE | ID: mdl-30842390

RESUMEN

BACKGROUND The aim of this study was to describe the case of a 27-year-old woman who developed Vogt-Koyanagi-Harada (VKH) disease in the 13th week of pregnancy, who was treated with high-dose oral corticosteroids and azathioprine due to its persistent course. CASE REPORT A 27-year-old East Indian woman in her 13th week of pregnancy presented with bilateral decreased visual acuity and metamorphopsia due to bilateral serous retinal detachments and was diagnosed with Vogt-Koyanagi-Harada (VKH) disease. Multimodal imaging, including blue light fundus autofluorescence (FAF), structural spectral domain optical coherence tomography (SD-OCT), en-face OCT, and OCT angiography (OCT-A), was performed at presentation and follow-up, being particularly helpful for identifying recurrences. Her treatment consisted of high-dose corticosteroid therapy, and azathioprine had to be added as an adjuvant due to the aggressive behavior of the disease. She gave birth to a healthy baby at 31 weeks of gestation and remained with 20/20 vision at 8 weeks postpartum. CONCLUSIONS To the best of our knowledge, this is the first report on the use of azathioprine in VKH disease during pregnancy with a successful outcome. Multimodal imaging avoiding the use of fundus fluorescein angiography is key in the diagnosis and follow-up of VKH disease in pregnant women.


Asunto(s)
Azatioprina/uso terapéutico , Inmunosupresores/uso terapéutico , Complicaciones del Embarazo/diagnóstico por imagen , Complicaciones del Embarazo/tratamiento farmacológico , Síndrome Uveomeningoencefálico/diagnóstico por imagen , Síndrome Uveomeningoencefálico/tratamiento farmacológico , Adulto , Angiografía , Femenino , Humanos , Imagen Multimodal , Embarazo , Primer Trimestre del Embarazo , Tomografía de Coherencia Óptica
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