Bilateral scleritis and sclerokeratitis associated with IgA nephropathy

Purpose The purpose of this study is to report a case of bilateral nodular scleritis in a patient with final diagnosis of IgA nephropathy. Methods This is an observational case report. Results A male patient, 42 years old, presented with a bilateral nodular scleritis and OD sclerokeratitis. He had a...

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Autores principales: Garza Leon, Manuel, Flores, Diana, Alarcón Galván, Gabriela, Sánchez Martínez, Concepción
Formato: Artículo
Lenguaje:inglés
Publicado: 2012
Acceso en línea:http://eprints.uanl.mx/14917/1/572.pdf
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author Garza Leon, Manuel
Flores, Diana
Alarcón Galván, Gabriela
Sánchez Martínez, Concepción
author_facet Garza Leon, Manuel
Flores, Diana
Alarcón Galván, Gabriela
Sánchez Martínez, Concepción
author_sort Garza Leon, Manuel
collection Repositorio Institucional
description Purpose The purpose of this study is to report a case of bilateral nodular scleritis in a patient with final diagnosis of IgA nephropathy. Methods This is an observational case report. Results A male patient, 42 years old, presented with a bilateral nodular scleritis and OD sclerokeratitis. He had a previous history of acute otitis media and developed posterior renal failure and arterial hypertension. Clinical and systemic findings suggest Wegener's granulomatosis. A kidney biopsy was performed, and immunoflourescence findings demonstrated granular deposits of IgA in a mesangial pattern confirming the diagnosis of IgA nephropathy Conclusions IgA nephropathy should be a differential diagnosis in patients with scleritis and nephropathy
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spelling eprints-149172019-06-14T14:54:09Z http://eprints.uanl.mx/14917/ Bilateral scleritis and sclerokeratitis associated with IgA nephropathy Garza Leon, Manuel Flores, Diana Alarcón Galván, Gabriela Sánchez Martínez, Concepción Purpose The purpose of this study is to report a case of bilateral nodular scleritis in a patient with final diagnosis of IgA nephropathy. Methods This is an observational case report. Results A male patient, 42 years old, presented with a bilateral nodular scleritis and OD sclerokeratitis. He had a previous history of acute otitis media and developed posterior renal failure and arterial hypertension. Clinical and systemic findings suggest Wegener's granulomatosis. A kidney biopsy was performed, and immunoflourescence findings demonstrated granular deposits of IgA in a mesangial pattern confirming the diagnosis of IgA nephropathy Conclusions IgA nephropathy should be a differential diagnosis in patients with scleritis and nephropathy 2012 Article PeerReviewed text en cc_by_nc_nd http://eprints.uanl.mx/14917/1/572.pdf http://eprints.uanl.mx/14917/1.haspreviewThumbnailVersion/572.pdf Garza Leon, Manuel y Flores, Diana y Alarcón Galván, Gabriela y Sánchez Martínez, Concepción (2012) Bilateral scleritis and sclerokeratitis associated with IgA nephropathy. Journal of Ophthalmic Inflammation and Infection, 2 (4). pp. 207-210. ISSN 1869-5760 http://doi.org/10.1007/s12348-012-0069-7 doi:10.1007/s12348-012-0069-7
spellingShingle Garza Leon, Manuel
Flores, Diana
Alarcón Galván, Gabriela
Sánchez Martínez, Concepción
Bilateral scleritis and sclerokeratitis associated with IgA nephropathy
thumbnail https://rediab.uanl.mx/themes/sandal5/images/online.png
title Bilateral scleritis and sclerokeratitis associated with IgA nephropathy
title_full Bilateral scleritis and sclerokeratitis associated with IgA nephropathy
title_fullStr Bilateral scleritis and sclerokeratitis associated with IgA nephropathy
title_full_unstemmed Bilateral scleritis and sclerokeratitis associated with IgA nephropathy
title_short Bilateral scleritis and sclerokeratitis associated with IgA nephropathy
title_sort bilateral scleritis and sclerokeratitis associated with iga nephropathy
url http://eprints.uanl.mx/14917/1/572.pdf
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AT alarcongalvangabriela bilateralscleritisandsclerokeratitisassociatedwithiganephropathy
AT sanchezmartinezconcepcion bilateralscleritisandsclerokeratitisassociatedwithiganephropathy