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1.
Med. infant ; 22(2): 83-87, Junio 2015. tab
Article de Espagnol | LILACS | ID: biblio-905817

RÉSUMÉ

Objetivo: Evaluar la respuesta al tratamiento con corticoides e inmunomoduladores en niños con pars planitis. Materiales y método: Se realiza un estudio retrospectivo y observacional de nueve historias clínicas de pacientes con diagnóstico de pars planitis atendidos en el servicio de oftalmología del Hospital de Pediatría Juan P. Garrahan desde el año 2010. Resultados: De los nueve pacientes 6 eran niños y 3 niñas. El motivo de consulta principal fue disminución de la visión. La mayoría de los pacientes fueron derivados por otros oftalmólogos para tratamiento. El 100% sufrió afectación ocular bilateral. Las complicaciones fueron: catarata, queratopatía en banda, hipertensión ocular y edema macular cistoide. El 100% de los pacientes recibió tratamiento con corticoides por vía oral e inmunomoduladores. A algunos se les efectuó inyecciones de triamcinolona subtenoniana y criocoagulación. Conclusiones: con el tratamiento con prednisona e inmunomoduladores se logró mejoría en la agudeza visual en 15 ojos y 3 ojos mantuvieron igual agudeza visual. La pars planitis es una patología crónica con un pronóstico visual reservado que requiere de un seguimiento estrecho y tratamiento prolongado por parte de un equipo interdisciplinario (AU)


Objective: To assess response to steroid and immunomodulating treatment in children with pars planitis. Material and methods: A retrospective observational study was conducted reviewing nine clinical charts of children with a diagnosis of pars planitis seen at the Department of Ophthalmology of the Pediatric Hospital Juan P. Garrahan since 2010. Results: Of nine patients, six were boys and three were girls. Main complaint was loss of vision. The majority of patients were referred to our hospital by other ophthalmologists for treatment. All children had bilateral eye involvement. Complications observed were: cataracts, band keratopathy, ocular hypertension, and cystoid macular edema. All patients received oral steroids and immunomodulating treatment. In some subtenonian injection of triamcinolone and cryocoagulation was performed. Conclusions: Prednisone and immunomodulating treatment resulted in an improvement of visual acuity in 15 eyes and three eyes visual acuity remained unchanged. Pars planitis is a chronic disease with an uncertain visual prognosis that requires close follow-up and prolonged treatment by an interdisciplinary team (AU)


Sujet(s)
Humains , Enfant d'âge préscolaire , Enfant , Adolescent , Hormones corticosurrénaliennes/usage thérapeutique , Maladies de la cornée/étiologie , Facteurs immunologiques/usage thérapeutique , Oedème maculaire/étiologie , Pars planite/complications , Pars planite/diagnostic , Pars planite/traitement médicamenteux , Maladie chronique
2.
Br J Ophthalmol ; 98(11): 1503-7, 2014 Nov.
Article de Anglais | MEDLINE | ID: mdl-24985727

RÉSUMÉ

AIM: To evaluate the clinical course of the patients with pars planitis that received immunosuppressive drugs. METHODS: We retrospectively analysed the data of 10 years from 374 patients with pars planitis in a large reference centre in Mexico City and included 49 patients (92 eyes). RESULTS: Median age at presentation was 8 years. 35 patients (71.4%) were male and 43 patients (87.7%) had bilateral disease. Diverse immunosuppressive medications were used, mainly methotrexate (69.4%) and azathioprine (63.3%) with 18 patients requiring more than one drug. The main indications for starting immunosuppressive therapy were lack of response to initial treatment and advance disease at presentation. The results showed good response with steroid reduction (69.3% of patients), visual acuity improvement (51% of patients) and inflammatory disease reduction (59.1% of patients). In 25 patients (51%), steroids were started previous to immunosuppressors and in 24 (49%) at the same time without significant difference in clinical improvement (p=0.210) or visual outcome (p=0.498). Thirteen patients (26.5%) presented mild adverse effects. The median of the final visual acuity was 20/40. The median follow-up time was 44 months (range 13-115 months). CONCLUSIONS: Immunosuppressive therapy allows an adequate control of inflammatory disease in pars planitis, with clinical and visual improvement and steroid dose reduction.


Sujet(s)
Immunosuppresseurs/usage thérapeutique , Pars planite/traitement médicamenteux , Adolescent , Adulte , Azathioprine/effets indésirables , Azathioprine/usage thérapeutique , Enfant , Enfant d'âge préscolaire , Cyclophosphamide/effets indésirables , Cyclophosphamide/usage thérapeutique , Ciclosporine/effets indésirables , Ciclosporine/usage thérapeutique , Femelle , Humains , Immunosuppresseurs/effets indésirables , Mâle , Méthotrexate/effets indésirables , Méthotrexate/usage thérapeutique , Mexique , Adulte d'âge moyen , Pars planite/diagnostic , Orientation vers un spécialiste , Études rétrospectives , Acuité visuelle
3.
Ocul Immunol Inflamm ; 11(1): 53-60, 2003 Mar.
Article de Anglais | MEDLINE | ID: mdl-12854027

RÉSUMÉ

PURPOSE: To describe the clinical manifestations of classic pars planitis (CPP) in Mexican patients. We report here the most frequent complications, medical and surgical treatment, and visual prognosis. MATERIAL AND METHODS: A retrospective, descriptive case series examined the clinical features, complications, and treatment (medical and surgical) of CPP patients seen at the Inflammatory Eye Disease Clinic from January 1990 to September 1999. RESULTS: One hundred and sixty patients met inclusion criteria for the study. Mean age at presentation was 10 years and males were more frequently affected. Both eyes were affected in 84.4% of the cases. The most frequent complaint was decreased visual acuity. Initial visual acuity (VA) ranged from no light perception to 20/20 (mean 20/50), and mean final VA was 20/30. The most frequent clinical manifestations were vitritis (99.7%), snowballs (99.3%), retinal vasculitis (89.2%), and snowbanks (63.1%). The most common complications were cystoid macular edema (63.4%) and cataract (47.5%). Periocular corticosteroids were used in 97.5% of cases, systemic corticosteroids in 68.1%, and other immunosuppressive drugs in 21.3%. CONCLUSIONS: CPP in the Mexican population is more frequent in males and usually presents in patients less than 14 years of age. It is typically bilateral, and the most common symptom is decreased visual acuity. The most important clinical findings are located in the vitreous and retina. Cataract and cystoid macular edema are the most frequent complications. Treatment comprises periocular and systemic corticosteroids or other immunosuppressive drugs.


Sujet(s)
Pars planite/complications , Pars planite/traitement médicamenteux , Acuité visuelle , Administration par voie topique , Adolescent , Adulte , Anti-inflammatoires/usage thérapeutique , Cataracte/étiologie , Enfant , Enfant d'âge préscolaire , Maladies de l'oeil/étiologie , Femelle , Glucocorticoïdes , Humains , Immunosuppresseurs/usage thérapeutique , Oedème maculaire/étiologie , Mâle , Mexique/épidémiologie , Pars planite/épidémiologie , Vascularite rétinienne/étiologie , Études rétrospectives , Troubles de la vision/étiologie , Corps vitré/anatomopathologie
5.
Rev. bras. oftalmol ; 54(2): 49-52, fev. 1995. ilus
Article de Portugais | LILACS | ID: lil-148566

RÉSUMÉ

Os autores relatam um caso de uveíte intermediária (pars planite) num paciente de 10 anos de idade submetido a tratamento clínico (corticoterapia tópica e antiinflamatório näo hormonal tópico por 14 meses) que persistiu com a mesma acuidade visual inicial. Os autores ressaltam a importância do cuidado com o tratamento, no sentido de evitar catarata, glaucoma e outras complicaçöes devido ao uso abusivo de esteróides (fator iatrogênico)


Sujet(s)
Humains , Enfant , Bétaxolol/pharmacologie , Dexaméthasone/pharmacologie , Pars planite/traitement médicamenteux , Timolol/pharmacologie
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