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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 ha...

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Autores principales: Garza-Leon, Manuel, Flores, Diana, Alarcón-Galván, Gabriela, Sánchez-Martínez, Concepción
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500980/
https://www.ncbi.nlm.nih.gov/pubmed/22411460
http://dx.doi.org/10.1007/s12348-012-0069-7
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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 PubMed
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 pubmed-35009802012-12-06 Bilateral scleritis and sclerokeratitis associated with IgA nephropathy Garza-Leon, Manuel Flores, Diana Alarcón-Galván, Gabriela Sánchez-Martínez, Concepción J Ophthalmic Inflamm Infect Brief Report 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. Springer-Verlag 2012-03-13 /pmc/articles/PMC3500980/ /pubmed/22411460 http://dx.doi.org/10.1007/s12348-012-0069-7 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Brief Report
Garza-Leon, Manuel
Flores, Diana
Alarcón-Galván, Gabriela
Sánchez-Martínez, Concepción
Bilateral scleritis and sclerokeratitis associated with IgA nephropathy
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
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500980/
https://www.ncbi.nlm.nih.gov/pubmed/22411460
http://dx.doi.org/10.1007/s12348-012-0069-7
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