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Cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report
Spontaneous intracranial hypotension is a rare clinical entity caused in most cases by a cerebrospinal fluid leak occurring at the level of the spinal cord. Cranial dural leaks have been previously reported as a cause of orthostatic headaches but, as opposed to spinal dural leaks, were not associate...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Carol Davila University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485374/ https://www.ncbi.nlm.nih.gov/pubmed/34621386 http://dx.doi.org/10.25122/jml-2021-0090 |
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author | Radu, Razvan Alexandru Terecoasa, Elena Oana Marinescu, Andreea Nicoleta Enache, Iulian Tiu, Cristina |
author_facet | Radu, Razvan Alexandru Terecoasa, Elena Oana Marinescu, Andreea Nicoleta Enache, Iulian Tiu, Cristina |
author_sort | Radu, Razvan Alexandru |
collection | PubMed |
description | Spontaneous intracranial hypotension is a rare clinical entity caused in most cases by a cerebrospinal fluid leak occurring at the level of the spinal cord. Cranial dural leaks have been previously reported as a cause of orthostatic headaches but, as opposed to spinal dural leaks, were not associated with other findings characteristic of spontaneous intracranial hypotension. We present the case of a male admitted for severe orthostatic headache. The patient had a history of intermittent postural headaches, dizziness, and symptoms consistent with post-nasal drip, which appeared several years after head trauma. Brain imaging showed signs consistent with intracranial hypotension: bilateral hygromas, subarachnoid hemorrhage, superficial siderosis, diffuse contrast enhancement of the pachymeninges, and superior sagittal sinus engorgement. No spinal leak could be identified by magnetic resonance imaging, and the patient had a rapid remission of symptoms with conservative management. Further work-up identified an old temporal bone fracture which created a route of egress between the posterior fossa and the mastoid cells. Otorhinolaryngology examination showed pulsatile bloody discharge and liquorrhea at the level of the left pharyngeal opening of the Eustachian tube. The orthostatic character of the headache, as well as the brain imaging findings, were consistent with intracranial hypotension syndrome caused by a cranial dural leak. Clinical signs and imaging findings consistent with the diagnosis of apparently “spontaneous” intracranial hypotension should prompt the search for a cranial dural leak if a spinal leak is not identified. |
format | Online Article Text |
id | pubmed-8485374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Carol Davila University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84853742021-10-06 Cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report Radu, Razvan Alexandru Terecoasa, Elena Oana Marinescu, Andreea Nicoleta Enache, Iulian Tiu, Cristina J Med Life Case Report Spontaneous intracranial hypotension is a rare clinical entity caused in most cases by a cerebrospinal fluid leak occurring at the level of the spinal cord. Cranial dural leaks have been previously reported as a cause of orthostatic headaches but, as opposed to spinal dural leaks, were not associated with other findings characteristic of spontaneous intracranial hypotension. We present the case of a male admitted for severe orthostatic headache. The patient had a history of intermittent postural headaches, dizziness, and symptoms consistent with post-nasal drip, which appeared several years after head trauma. Brain imaging showed signs consistent with intracranial hypotension: bilateral hygromas, subarachnoid hemorrhage, superficial siderosis, diffuse contrast enhancement of the pachymeninges, and superior sagittal sinus engorgement. No spinal leak could be identified by magnetic resonance imaging, and the patient had a rapid remission of symptoms with conservative management. Further work-up identified an old temporal bone fracture which created a route of egress between the posterior fossa and the mastoid cells. Otorhinolaryngology examination showed pulsatile bloody discharge and liquorrhea at the level of the left pharyngeal opening of the Eustachian tube. The orthostatic character of the headache, as well as the brain imaging findings, were consistent with intracranial hypotension syndrome caused by a cranial dural leak. Clinical signs and imaging findings consistent with the diagnosis of apparently “spontaneous” intracranial hypotension should prompt the search for a cranial dural leak if a spinal leak is not identified. Carol Davila University Press 2021 /pmc/articles/PMC8485374/ /pubmed/34621386 http://dx.doi.org/10.25122/jml-2021-0090 Text en ©2021 JOURNAL of MEDICINE and LIFE https://creativecommons.org/licenses/by/3.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Case Report Radu, Razvan Alexandru Terecoasa, Elena Oana Marinescu, Andreea Nicoleta Enache, Iulian Tiu, Cristina Cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report |
title | Cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report |
title_full | Cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report |
title_fullStr | Cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report |
title_full_unstemmed | Cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report |
title_short | Cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report |
title_sort | cranial cerebrospinal fluid leak and intracranial hypotension syndrome – a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485374/ https://www.ncbi.nlm.nih.gov/pubmed/34621386 http://dx.doi.org/10.25122/jml-2021-0090 |
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