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Idiopathic intracranial hypertension in child

We present the case of a 12-year-old boy with bilateral papilledema, relating moderate symptomatology and without an important medical history. Ophthalmological examination revealed a significant alteration of visual acuity, an important papilledema and macular edema in both eyes. Further investigat...

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Autores principales: Zemba, Mihail, Dimirache, Andreea-Elena, Rogoz, Roxana-Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Romanian Society of Ophthalmology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739010/
https://www.ncbi.nlm.nih.gov/pubmed/33367182
http://dx.doi.org/10.22336/rjo.2020.66
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author Zemba, Mihail
Dimirache, Andreea-Elena
Rogoz, Roxana-Elena
author_facet Zemba, Mihail
Dimirache, Andreea-Elena
Rogoz, Roxana-Elena
author_sort Zemba, Mihail
collection PubMed
description We present the case of a 12-year-old boy with bilateral papilledema, relating moderate symptomatology and without an important medical history. Ophthalmological examination revealed a significant alteration of visual acuity, an important papilledema and macular edema in both eyes. Further investigations excluded infectious and autoimmune diseases, intracranial masses and congenital affliction. Because of an elevated opening pressure in lumbar puncture procedure, the diagnosis of intracranial hypertension was confirmed. After two weeks of treatment with corticosteroids, carbonic anhydrase inhibitor and hyperosmotic drug, the patient had an important structural and functional ophthalmological improvement.
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spelling pubmed-77390102020-12-22 Idiopathic intracranial hypertension in child Zemba, Mihail Dimirache, Andreea-Elena Rogoz, Roxana-Elena Rom J Ophthalmol Case Reports We present the case of a 12-year-old boy with bilateral papilledema, relating moderate symptomatology and without an important medical history. Ophthalmological examination revealed a significant alteration of visual acuity, an important papilledema and macular edema in both eyes. Further investigations excluded infectious and autoimmune diseases, intracranial masses and congenital affliction. Because of an elevated opening pressure in lumbar puncture procedure, the diagnosis of intracranial hypertension was confirmed. After two weeks of treatment with corticosteroids, carbonic anhydrase inhibitor and hyperosmotic drug, the patient had an important structural and functional ophthalmological improvement. Romanian Society of Ophthalmology 2020 /pmc/articles/PMC7739010/ /pubmed/33367182 http://dx.doi.org/10.22336/rjo.2020.66 Text en ©Romanian Society of Ophthalmology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Zemba, Mihail
Dimirache, Andreea-Elena
Rogoz, Roxana-Elena
Idiopathic intracranial hypertension in child
title Idiopathic intracranial hypertension in child
title_full Idiopathic intracranial hypertension in child
title_fullStr Idiopathic intracranial hypertension in child
title_full_unstemmed Idiopathic intracranial hypertension in child
title_short Idiopathic intracranial hypertension in child
title_sort idiopathic intracranial hypertension in child
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739010/
https://www.ncbi.nlm.nih.gov/pubmed/33367182
http://dx.doi.org/10.22336/rjo.2020.66
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