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1.
Arch Soc Esp Oftalmol (Engl Ed) ; 96(11): 593-597, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34756281

ABSTRACT

The case is presented on a young Honduran female with no medical history of note, who presented with multiple areas of exudative retinal detachment (RD), and a best-corrected visual acuity of 1.3 logMAR in both eyes. She was diagnosed with incomplete Vogt-Koyanagi-Harada syndrome, and treated early with a combination of intravenous therapy with 1 g of prednisolone per day for 3 days, as recommended by published evidence, as well as mycophenolate mofetil (2 g per day). During the corticosteroids tapering, there was a recurrence of exudative retinal detachments, and megadoses of 1 g of intravenous corticosteroids per day were reintroduced for 6 days until the complete resolution of the fluid of the exudative RD, and cyclosporine (100 mg per day), subtenon triamcinolone (40 mg/mL), and intravitreal ranibizumab once a month in the both eyes were added to the treatment, with a great control of choroidal inflammation that resulted in the remission of symptoms and signs.


Subject(s)
Mycophenolic Acid , Uveomeningoencephalitic Syndrome , Adrenal Cortex Hormones/therapeutic use , Female , Fluorescein Angiography , Humans , Mycophenolic Acid/therapeutic use , Uveomeningoencephalitic Syndrome/drug therapy , Visual Acuity
2.
Arch. Soc. Esp. Oftalmol ; 96(11): 593-597, nov. 2021.
Article in Spanish | IBECS | ID: ibc-218284

ABSTRACT

Presentamos el caso de una mujer hondureña de 27 años sin antecedentes médicos de interés que presentó múltiples áreas de desprendimientos de retina (DR) exudativos y una mejor agudeza visual corregida de 1,3logMAR en ambos ojos. Fue diagnosticada de síndrome de Vogt-Koyanagi-Harada incompleto y tratada con prednisolona intravenosa (1g/24h) durante 3 días, tal y como recomienda la evidencia publicada, junto con micofenolato de mofetilo (2g/24h). Durante el descenso paulatino de corticoesteroides, los DR recidivaron, por lo que se reintrodujeron las megadosis de 1g/24h de corticoesteroides intravenosos durante 6 días hasta la resolución completa de los DR y se añadieron ciclosporina (100mg/24h), triamcinolona subtenoniana (40mg/mL) e inyecciones intravítreas mensuales de ranibizumab en ambos ojos, con un adecuado control de la inflamación coroidea que se tradujo en la remisión de los síntomas y signos (AU)


The case is presented on a young Honduran female with no medical history of note, who presented with multiple areas of exudative retinal detachment (RD), and a best-corrected visual acuity of 1.3logMAR in both eyes. She was diagnosed with incomplete Vogt-Koyanagi-Harada syndrome, and treated early with a combination of intravenous therapy with 1g of prednisolone per day for 3 days, as recommended by published evidence, as well as mycophenolate mofetil (2g per day). During the corticosteroids tapering, there was a recurrence of exudative retinal detachments, and megadoses of 1g of intravenous corticosteroids per day were reintroduced for 6 days until the complete resolution of the fluid of the exudative RD, and cyclosporine (100mg per day), subtenon triamcinolone (40mg/mL), and intravitreal ranibizumab once a month in the both eyes were added to the treatment, with a great control of choroidal inflammation that resulted in the remission of symptoms and signs (AU)


Subject(s)
Humans , Female , Adult , Uveomeningoencephalitic Syndrome/drug therapy , Mycophenolic Acid/therapeutic use , Adrenal Cortex Hormones/administration & dosage , Mycophenolic Acid/administration & dosage , Treatment Outcome , Fluorescein Angiography , Visual Acuity
3.
Article in English, Spanish | MEDLINE | ID: mdl-33036807

ABSTRACT

The case is presented on a young Honduran female with no medical history of note, who presented with multiple areas of exudative retinal detachment (RD), and a best-corrected visual acuity of 1.3logMAR in both eyes. She was diagnosed with incomplete Vogt-Koyanagi-Harada syndrome, and treated early with a combination of intravenous therapy with 1g of prednisolone per day for 3 days, as recommended by published evidence, as well as mycophenolate mofetil (2g per day). During the corticosteroids tapering, there was a recurrence of exudative retinal detachments, and megadoses of 1g of intravenous corticosteroids per day were reintroduced for 6 days until the complete resolution of the fluid of the exudative RD, and cyclosporine (100mg per day), subtenon triamcinolone (40mg/mL), and intravitreal ranibizumab once a month in the both eyes were added to the treatment, with a great control of choroidal inflammation that resulted in the remission of symptoms and signs.

7.
J Fr Ophtalmol ; 42(1): 63-72, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30594420

ABSTRACT

A retinal pigment epithelial (RPE) tear is a well-known complication of retinal pigment epithelial detachments (PED) and may cause a significant visual impairment. The most common cause is a vascularized PED in patients with exudative age-related macular degeneration (AMD). The development of diagnostic imaging techniques brings us closer to the etiology and pathophysiological mechanisms of this entity, offering us new strategies for treatment and follow-up. The advent of intravitreal antiangiogenic treatment (anti-VEGF) has led to an increase in the number of reported cases of RPE tears, which are an important vision-limiting factor during treatment. However, RPE tears may occur spontaneously or as a consequence of thermal laser treatment, photodynamic therapy or anti-VEGF therapy. It is accepted that the mechanism of RPE tears is multifactorial. The optimization of the functional outcome of this complication has been described with continuous treatment with antiangiogenic drugs. The goal of the present review is to evaluate the incidence, risk factors and treatment of RPE tears.


Subject(s)
Retinal Perforations , Retinal Pigment Epithelium/injuries , Diagnostic Imaging/methods , Humans , Retinal Detachment/complications , Retinal Detachment/diagnosis , Retinal Detachment/epidemiology , Retinal Detachment/therapy , Retinal Perforations/diagnosis , Retinal Perforations/epidemiology , Retinal Perforations/etiology , Retinal Perforations/therapy , Retinal Pigment Epithelium/diagnostic imaging , Retinal Pigment Epithelium/surgery , Risk Factors , Rupture, Spontaneous/diagnosis , Rupture, Spontaneous/epidemiology , Rupture, Spontaneous/etiology , Rupture, Spontaneous/therapy
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