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Idiopathic Intracranial Hypertension: A Case Report

Idiopathic Intracranial Hypertension (IIH) is a rare occurrence in young, physically fit male and a diagnosis of exclusion among most patients presenting with signs and symptoms of raised intracranial pressure. Here we describe a case of a young male in the ideal weight range with no previous exposu...

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Autores principales: Ghimire, Anupam, Acharya, Achal Raj, Karn, Anish, Jha, Mukesh Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of the Nepal Medical Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959236/
https://www.ncbi.nlm.nih.gov/pubmed/34506475
http://dx.doi.org/10.31729/jnma.5176
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author Ghimire, Anupam
Acharya, Achal Raj
Karn, Anish
Jha, Mukesh Kumar
author_facet Ghimire, Anupam
Acharya, Achal Raj
Karn, Anish
Jha, Mukesh Kumar
author_sort Ghimire, Anupam
collection PubMed
description Idiopathic Intracranial Hypertension (IIH) is a rare occurrence in young, physically fit male and a diagnosis of exclusion among most patients presenting with signs and symptoms of raised intracranial pressure. Here we describe a case of a young male in the ideal weight range with no previous exposure to offending chemicals presented with a history of headache, obscuration of vision, and photopsia. On examination, there were no positive neurological findings. Increased opening pressure was found on the lumbar puncture. Ophthalmological examination revealed bilateral papilledema. Humphrey's Visual field test showed peripheral field loss. MRI scan of the brain and orbits were normal. The patient was diagnosed and managed in primary care setting after neurosurgical consultation. Though rare, we should suspect IIH in ideal body weighted male if the headache is persistent after other causes of headache have been ruled out.
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spelling pubmed-89592362022-04-14 Idiopathic Intracranial Hypertension: A Case Report Ghimire, Anupam Acharya, Achal Raj Karn, Anish Jha, Mukesh Kumar JNMA J Nepal Med Assoc Case Report Idiopathic Intracranial Hypertension (IIH) is a rare occurrence in young, physically fit male and a diagnosis of exclusion among most patients presenting with signs and symptoms of raised intracranial pressure. Here we describe a case of a young male in the ideal weight range with no previous exposure to offending chemicals presented with a history of headache, obscuration of vision, and photopsia. On examination, there were no positive neurological findings. Increased opening pressure was found on the lumbar puncture. Ophthalmological examination revealed bilateral papilledema. Humphrey's Visual field test showed peripheral field loss. MRI scan of the brain and orbits were normal. The patient was diagnosed and managed in primary care setting after neurosurgical consultation. Though rare, we should suspect IIH in ideal body weighted male if the headache is persistent after other causes of headache have been ruled out. Journal of the Nepal Medical Association 2021-02 2021-02-28 /pmc/articles/PMC8959236/ /pubmed/34506475 http://dx.doi.org/10.31729/jnma.5176 Text en © The Author(s) 2018. https://creativecommons.org/licenses/by/4.0/This is an Open-Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ghimire, Anupam
Acharya, Achal Raj
Karn, Anish
Jha, Mukesh Kumar
Idiopathic Intracranial Hypertension: A Case Report
title Idiopathic Intracranial Hypertension: A Case Report
title_full Idiopathic Intracranial Hypertension: A Case Report
title_fullStr Idiopathic Intracranial Hypertension: A Case Report
title_full_unstemmed Idiopathic Intracranial Hypertension: A Case Report
title_short Idiopathic Intracranial Hypertension: A Case Report
title_sort idiopathic intracranial hypertension: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959236/
https://www.ncbi.nlm.nih.gov/pubmed/34506475
http://dx.doi.org/10.31729/jnma.5176
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