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1.
J Med Case Rep ; 16(1): 338, 2022 Sep 06.
Artículo en Inglés | MEDLINE | ID: mdl-36064601

RESUMEN

BACKGROUND: Solar maculopathy is a well described clinical entity that usually occurs in patients that have gazed directly the sun. In this report we describe the first two cases of solar maculopathy in individuals exposed to sunlight reflected from the screen of mobile devices in the absence of direct sun gaze. CASES DESCRIPTION: Case 1. A 30-year-old Caucasic man presented with bilateral metamorphopsia, central scotoma and decreased visual acuity two days after being reading for four hours with his tablet computer in a terrace of a ski center. CASE 2: A 20-year-old Caucasic woman was examined for bilateral decrease of visual acuity and central scotoma after being at the beach the day before and reading with her mobile phone for 3 hours. Both patients denied gazing directly to sunlight at any moment. In each case, exploration revealed fundus and OCT images compatible with the typical features of solar maculopathy. After 2 years of follow-up, in absence of any specific treatment, Case 1 had a complete resolution of the fundus alterations, while Case 2 still presented defects of the outer retinal layers. In both cases, an exposure to sunlight reflected from the screen of their mobile devices was documented in environments where solar radiation is thought to be augmented. CONCLUSION: Sunlight reflection from a display screen needs to be considered as a possible risk factor for increased solar radiation and a subsequent risk of solar maculopathy.


Asunto(s)
Degeneración Macular , Enfermedades de la Retina , Adulto , Femenino , Humanos , Degeneración Macular/complicaciones , Degeneración Macular/etiología , Masculino , Enfermedades de la Retina/diagnóstico , Enfermedades de la Retina/etiología , Escotoma/diagnóstico , Escotoma/etiología , Luz Solar/efectos adversos , Tomografía de Coherencia Óptica , Adulto Joven
2.
Eye (Lond) ; 35(2): 425-432, 2021 02.
Artículo en Inglés | MEDLINE | ID: mdl-32291404

RESUMEN

BACKGROUND/OBJECTIVES: To analyze the ophthalmic characteristics of congenital prepapillary vascular loop (PVL) and to propose a new morphologic classification dividing the loops into six types. SUBJECTS/METHODS: Collaborative multinational multicentre retrospective study of PVL cases. RESULTS: There was a total of 49 cases (61 eyes), 37 unilateral (75.5%) and 12 bilateral (24.5%), 32 arterial type (65.3%) and 18 venous type (36.7%) (one patient had either kind in each eye). The mean number of loops per eye was 2.7 (range, 1-7). The loops were asymptomatic in 42 cases (85.7%). Other findings included: the presence of cilioretinal artery (14 cases), retinal vascular tortuosity (26 cases), amaurosis fugax (1 case), branch retinal artery occlusion (1 case) and vitreous haemorrhage (3 cases). Six morphologic loop types could be discerned based on elevation (flat vs. elevated), shape (figure of 8 or corkscrew with hyaline sheath), number (multiple or single), location (central or peripheral), lumen size (arterial vs. arteriolar) and presence of vascular tortuosity or vitreous traction. CONCLUSIONS: PVL are usually asymptomatic and can be divided into six morphologic types with different pathogenesis during early embryogenesis.


Asunto(s)
Anomalías del Ojo , Malformaciones Vasculares , Humanos , Vasos Retinianos/anomalías , Estudios Retrospectivos , Malformaciones Vasculares/diagnóstico
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