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Spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature
BACKGROUND: Idiopathic intracranial hypertension can lead to dural defects and spontaneous leakage of cerebrospinal fluid (CSF) from the skull base. Skull base CSF leaks are rarely reported in pregnancy but pose unique challenges for obstetricians and anesthesiologists. CASE PRESENTATION: A 31-year-...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993356/ https://www.ncbi.nlm.nih.gov/pubmed/36890487 http://dx.doi.org/10.1186/s12884-023-05460-5 |
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author | Michelle, Lauren Post, Rebecca J. Kuan, Edward C. Nageotte, Michael P. |
author_facet | Michelle, Lauren Post, Rebecca J. Kuan, Edward C. Nageotte, Michael P. |
author_sort | Michelle, Lauren |
collection | PubMed |
description | BACKGROUND: Idiopathic intracranial hypertension can lead to dural defects and spontaneous leakage of cerebrospinal fluid (CSF) from the skull base. Skull base CSF leaks are rarely reported in pregnancy but pose unique challenges for obstetricians and anesthesiologists. CASE PRESENTATION: A 31-year-old G4P1021 at 14 weeks developed debilitating headaches and CSF rhinorrhea. Brain imaging revealed a bony defect of the sphenoid sinus with a meningoencephalocele and a partially empty sella, consistent with CSF leakage from a skull base defect. The patient was neurologically stable without signs of meningitis; thus, management was focused on symptomatic alleviation. A planned cesarean section was performed at 38 weeks under spinal anesthesia. The patient had spontaneous marked improvement of her symptoms postpartum. CONCLUSION: Pregnancy may exacerbate skull base CSF leaks, requiring careful management with a multidisciplinary team. Neuraxial anesthesia can safely be performed in pregnant individuals with spontaneous skull base CSF leakage, but further studies are needed to determine the safest mode of delivery in these patients. |
format | Online Article Text |
id | pubmed-9993356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99933562023-03-08 Spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature Michelle, Lauren Post, Rebecca J. Kuan, Edward C. Nageotte, Michael P. BMC Pregnancy Childbirth Case Report BACKGROUND: Idiopathic intracranial hypertension can lead to dural defects and spontaneous leakage of cerebrospinal fluid (CSF) from the skull base. Skull base CSF leaks are rarely reported in pregnancy but pose unique challenges for obstetricians and anesthesiologists. CASE PRESENTATION: A 31-year-old G4P1021 at 14 weeks developed debilitating headaches and CSF rhinorrhea. Brain imaging revealed a bony defect of the sphenoid sinus with a meningoencephalocele and a partially empty sella, consistent with CSF leakage from a skull base defect. The patient was neurologically stable without signs of meningitis; thus, management was focused on symptomatic alleviation. A planned cesarean section was performed at 38 weeks under spinal anesthesia. The patient had spontaneous marked improvement of her symptoms postpartum. CONCLUSION: Pregnancy may exacerbate skull base CSF leaks, requiring careful management with a multidisciplinary team. Neuraxial anesthesia can safely be performed in pregnant individuals with spontaneous skull base CSF leakage, but further studies are needed to determine the safest mode of delivery in these patients. BioMed Central 2023-03-08 /pmc/articles/PMC9993356/ /pubmed/36890487 http://dx.doi.org/10.1186/s12884-023-05460-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Michelle, Lauren Post, Rebecca J. Kuan, Edward C. Nageotte, Michael P. Spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature |
title | Spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature |
title_full | Spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature |
title_fullStr | Spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature |
title_full_unstemmed | Spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature |
title_short | Spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature |
title_sort | spontaneous skull base cerebrospinal fluid leak during pregnancy: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993356/ https://www.ncbi.nlm.nih.gov/pubmed/36890487 http://dx.doi.org/10.1186/s12884-023-05460-5 |
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