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Nummular keratopathy in a patient with Hyper-IgD Syndrome

PURPOSE: To report a case of recurrent nummular keratitis in a pediatric patient with Hyperimmunoglobulinemia D syndrome. METHODS: A retrospective chart review. RESULTS: A 14-year-old boy with Hyperimmunoglobulinemia D syndrome (HIDS) presented with photophobia and ocular irritation concomitant with...

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Autores principales: Kraus, Courtney L, Culican, Susan M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731058/
https://www.ncbi.nlm.nih.gov/pubmed/19656398
http://dx.doi.org/10.1186/1546-0096-7-14
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author Kraus, Courtney L
Culican, Susan M
author_facet Kraus, Courtney L
Culican, Susan M
author_sort Kraus, Courtney L
collection PubMed
description PURPOSE: To report a case of recurrent nummular keratitis in a pediatric patient with Hyperimmunoglobulinemia D syndrome. METHODS: A retrospective chart review. RESULTS: A 14-year-old boy with Hyperimmunoglobulinemia D syndrome (HIDS) presented with photophobia and ocular irritation concomitant with disease exacerbation. He was found on exam to have significant nummular keratitis, which responded to a short course of topical steroids. Despite acute response to local immunosuppression, the patient had several recurrent attacks and eventually developed a large corneal scar and decreased vision. After initiation of infliximab therapy his ocular sequelae improved dramatically and his vision returned to 20/20. CONCLUSION: One possible form of end-organ damage associated with HIDS is vision threatening nummular keratopathy.
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spelling pubmed-27310582009-08-24 Nummular keratopathy in a patient with Hyper-IgD Syndrome Kraus, Courtney L Culican, Susan M Pediatr Rheumatol Online J Case Report PURPOSE: To report a case of recurrent nummular keratitis in a pediatric patient with Hyperimmunoglobulinemia D syndrome. METHODS: A retrospective chart review. RESULTS: A 14-year-old boy with Hyperimmunoglobulinemia D syndrome (HIDS) presented with photophobia and ocular irritation concomitant with disease exacerbation. He was found on exam to have significant nummular keratitis, which responded to a short course of topical steroids. Despite acute response to local immunosuppression, the patient had several recurrent attacks and eventually developed a large corneal scar and decreased vision. After initiation of infliximab therapy his ocular sequelae improved dramatically and his vision returned to 20/20. CONCLUSION: One possible form of end-organ damage associated with HIDS is vision threatening nummular keratopathy. BioMed Central 2009-08-05 /pmc/articles/PMC2731058/ /pubmed/19656398 http://dx.doi.org/10.1186/1546-0096-7-14 Text en Copyright © 2009 Kraus and Culican; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kraus, Courtney L
Culican, Susan M
Nummular keratopathy in a patient with Hyper-IgD Syndrome
title Nummular keratopathy in a patient with Hyper-IgD Syndrome
title_full Nummular keratopathy in a patient with Hyper-IgD Syndrome
title_fullStr Nummular keratopathy in a patient with Hyper-IgD Syndrome
title_full_unstemmed Nummular keratopathy in a patient with Hyper-IgD Syndrome
title_short Nummular keratopathy in a patient with Hyper-IgD Syndrome
title_sort nummular keratopathy in a patient with hyper-igd syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731058/
https://www.ncbi.nlm.nih.gov/pubmed/19656398
http://dx.doi.org/10.1186/1546-0096-7-14
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