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Benign Intracranial Hypertension: A Diagnostic Dilemma

Benign intracranial hypertension (BIH) (also known as pseudotumor cerebri and empty sella syndrome) remains a diagnostic challenge to most physicians. The modified Dandy criteria consist of, the classic findings of headache, pulsatile tinnitus, papilledema, and elevated cerebrospinal fluid (CSF) pre...

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Autores principales: Shaw, Gary Y., Million, Stephanie K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423822/
https://www.ncbi.nlm.nih.gov/pubmed/22928139
http://dx.doi.org/10.1155/2012/814696
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author Shaw, Gary Y.
Million, Stephanie K.
author_facet Shaw, Gary Y.
Million, Stephanie K.
author_sort Shaw, Gary Y.
collection PubMed
description Benign intracranial hypertension (BIH) (also known as pseudotumor cerebri and empty sella syndrome) remains a diagnostic challenge to most physicians. The modified Dandy criteria consist of, the classic findings of headache, pulsatile tinnitus, papilledema, and elevated cerebrospinal fluid (CSF) pressure, however, these are rarely collectively present in any one patient. Furthermore, these findings can wax and wane over time. Due to the nature of this disease, both signs and symptoms may be intermittent, making definitive diagnosis difficult. Newer imaging studies, particularly the magnetic resonance venogram (MRV) along with a constellation of correlative findings and associated diseases have given new impetus in the diagnosis, treatment, and pathophysiology of this disease. This has led the authors to offer modifications to the classic Dandy criteria. This report presents three representative cases of BIH highlighting many of the newer advances in both diagnosis and treatment of this perplexing disorder.
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spelling pubmed-34238222012-08-27 Benign Intracranial Hypertension: A Diagnostic Dilemma Shaw, Gary Y. Million, Stephanie K. Case Rep Otolaryngol Case Report Benign intracranial hypertension (BIH) (also known as pseudotumor cerebri and empty sella syndrome) remains a diagnostic challenge to most physicians. The modified Dandy criteria consist of, the classic findings of headache, pulsatile tinnitus, papilledema, and elevated cerebrospinal fluid (CSF) pressure, however, these are rarely collectively present in any one patient. Furthermore, these findings can wax and wane over time. Due to the nature of this disease, both signs and symptoms may be intermittent, making definitive diagnosis difficult. Newer imaging studies, particularly the magnetic resonance venogram (MRV) along with a constellation of correlative findings and associated diseases have given new impetus in the diagnosis, treatment, and pathophysiology of this disease. This has led the authors to offer modifications to the classic Dandy criteria. This report presents three representative cases of BIH highlighting many of the newer advances in both diagnosis and treatment of this perplexing disorder. Hindawi Publishing Corporation 2012 2012-08-09 /pmc/articles/PMC3423822/ /pubmed/22928139 http://dx.doi.org/10.1155/2012/814696 Text en Copyright © 2012 G. Y. Shaw and S. K. Million. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Shaw, Gary Y.
Million, Stephanie K.
Benign Intracranial Hypertension: A Diagnostic Dilemma
title Benign Intracranial Hypertension: A Diagnostic Dilemma
title_full Benign Intracranial Hypertension: A Diagnostic Dilemma
title_fullStr Benign Intracranial Hypertension: A Diagnostic Dilemma
title_full_unstemmed Benign Intracranial Hypertension: A Diagnostic Dilemma
title_short Benign Intracranial Hypertension: A Diagnostic Dilemma
title_sort benign intracranial hypertension: a diagnostic dilemma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423822/
https://www.ncbi.nlm.nih.gov/pubmed/22928139
http://dx.doi.org/10.1155/2012/814696
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