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Persistent Cerebrospinal Fluid Leukocytosis: Could this be Idiopathic Intracranial Hypertension?
A 37-year-old female, a known epileptic, presented to the neurology clinic with a seven-day history of persistent bilateral headache not improving with analgesics. Her neurological and systemic examinations were unremarkable except for right optic disc edema. Magnetic resonance imaging (MRI) brain a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609303/ https://www.ncbi.nlm.nih.gov/pubmed/31309030 http://dx.doi.org/10.7759/cureus.4607 |
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author | Malik, Waseem T Ali, Rubab Shah, Aun R |
author_facet | Malik, Waseem T Ali, Rubab Shah, Aun R |
author_sort | Malik, Waseem T |
collection | PubMed |
description | A 37-year-old female, a known epileptic, presented to the neurology clinic with a seven-day history of persistent bilateral headache not improving with analgesics. Her neurological and systemic examinations were unremarkable except for right optic disc edema. Magnetic resonance imaging (MRI) brain and magnetic resonance venography (MRV) were normal but her cerebrospinal fluid (CSF) opening pressure was 280 mm of water with a CSF white cell count of 214. The patient showed improvement following treatment with intravenous antibiotics and acyclovir. She returned a week later with double vision and blurring in both eyes. Examination showed bilateral sixth nerve palsies and bilateral optic disc edema with left fundal hemorrhages. The spinal tap was repeated again, which showed a CSF opening pressure of 500 mm of water and the white cell count was 48. Extensive investigations for etiologies were mostly unrevealing. The patient was started on acetazolamide and topiramate combined with a large-volume therapeutic CSF tap. She continued to improve subsequently and was at the baseline functional state at three months, with complete resolution of hemorrhages and optic disc edema. Idiopathic intracranial hypertension (IIH) may present with persistent abnormal CSF with a high white cell count. Therefore, this must be diagnosed with caution, as it may be misdiagnosed and wrongly treated for other causes. |
format | Online Article Text |
id | pubmed-6609303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-66093032019-07-15 Persistent Cerebrospinal Fluid Leukocytosis: Could this be Idiopathic Intracranial Hypertension? Malik, Waseem T Ali, Rubab Shah, Aun R Cureus Internal Medicine A 37-year-old female, a known epileptic, presented to the neurology clinic with a seven-day history of persistent bilateral headache not improving with analgesics. Her neurological and systemic examinations were unremarkable except for right optic disc edema. Magnetic resonance imaging (MRI) brain and magnetic resonance venography (MRV) were normal but her cerebrospinal fluid (CSF) opening pressure was 280 mm of water with a CSF white cell count of 214. The patient showed improvement following treatment with intravenous antibiotics and acyclovir. She returned a week later with double vision and blurring in both eyes. Examination showed bilateral sixth nerve palsies and bilateral optic disc edema with left fundal hemorrhages. The spinal tap was repeated again, which showed a CSF opening pressure of 500 mm of water and the white cell count was 48. Extensive investigations for etiologies were mostly unrevealing. The patient was started on acetazolamide and topiramate combined with a large-volume therapeutic CSF tap. She continued to improve subsequently and was at the baseline functional state at three months, with complete resolution of hemorrhages and optic disc edema. Idiopathic intracranial hypertension (IIH) may present with persistent abnormal CSF with a high white cell count. Therefore, this must be diagnosed with caution, as it may be misdiagnosed and wrongly treated for other causes. Cureus 2019-05-07 /pmc/articles/PMC6609303/ /pubmed/31309030 http://dx.doi.org/10.7759/cureus.4607 Text en Copyright © 2019, Malik et al. http://creativecommons.org/licenses/by/3.0/ 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 author and source are credited. |
spellingShingle | Internal Medicine Malik, Waseem T Ali, Rubab Shah, Aun R Persistent Cerebrospinal Fluid Leukocytosis: Could this be Idiopathic Intracranial Hypertension? |
title | Persistent Cerebrospinal Fluid Leukocytosis: Could this be Idiopathic Intracranial Hypertension? |
title_full | Persistent Cerebrospinal Fluid Leukocytosis: Could this be Idiopathic Intracranial Hypertension? |
title_fullStr | Persistent Cerebrospinal Fluid Leukocytosis: Could this be Idiopathic Intracranial Hypertension? |
title_full_unstemmed | Persistent Cerebrospinal Fluid Leukocytosis: Could this be Idiopathic Intracranial Hypertension? |
title_short | Persistent Cerebrospinal Fluid Leukocytosis: Could this be Idiopathic Intracranial Hypertension? |
title_sort | persistent cerebrospinal fluid leukocytosis: could this be idiopathic intracranial hypertension? |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609303/ https://www.ncbi.nlm.nih.gov/pubmed/31309030 http://dx.doi.org/10.7759/cureus.4607 |
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