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Spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: A case report

BACKGROUND: Spinal cerebrospinal fluid venous fistula (CVF) is a recognized cause of chronic positional headache and spontaneous intracranial hypotension (SIH). It occurs due to an aberrant connection formed between the spinal subarachnoid space and an adjacent spinal epidural vein. The diagnosis of...

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Autores principales: Aljuboori, Zaid, McGrath, Margaret, Essibayi, Muhammed Amir, Zaidi, Saif, Hallam, Danial, Ghodke, Basavaraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571307/
https://www.ncbi.nlm.nih.gov/pubmed/34754542
http://dx.doi.org/10.25259/SNI_878_2021
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author Aljuboori, Zaid
McGrath, Margaret
Essibayi, Muhammed Amir
Zaidi, Saif
Hallam, Danial
Ghodke, Basavaraj
author_facet Aljuboori, Zaid
McGrath, Margaret
Essibayi, Muhammed Amir
Zaidi, Saif
Hallam, Danial
Ghodke, Basavaraj
author_sort Aljuboori, Zaid
collection PubMed
description BACKGROUND: Spinal cerebrospinal fluid venous fistula (CVF) is a recognized cause of chronic positional headache and spontaneous intracranial hypotension (SIH). It occurs due to an aberrant connection formed between the spinal subarachnoid space and an adjacent spinal epidural vein. The diagnosis of CVF can be difficult to establish but can be documented utilizing advanced imaging techniques (e.g., enhanced MR myelography/digital subtraction myelography). Their treatment involves surgical ligation of the involved nerve root, imaging-guided epidural blood patching, and/or endovascular embolization. Here, we report a 40-year-old male who presented with a symptomatic lumbar CVF successfully treated with transvenous embolization. CASE DESCRIPTION: A 40-year-old male presented with several months of positional headaches. The MRI of the brain showed diffuse pachymeningeal enhancement consistent with the diagnosis of SIH. Although the MR of the lumbar spine was unremarkable, the MR myelogram with digital subtraction imaging showed a CVF at the L2 level. Following transvenous embolization (i.e., through the Azygous vein), the patient’s symptoms fully resolved. CONCLUSION: Spinal CVF are rare and may cause chronic headaches and symptoms/signs of SIH. In this case, an MR myelogram with digital subtraction images demonstrated the anomalous connection between the spinal subarachnoid space and an adjacent spinal epidural vein at the L2 level. Although open surgical ablation of this connection may be feasible, less invasive techniques such as endovascular embolization should become the treatment of choice for the future management of CVF.
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spelling pubmed-85713072021-11-08 Spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: A case report Aljuboori, Zaid McGrath, Margaret Essibayi, Muhammed Amir Zaidi, Saif Hallam, Danial Ghodke, Basavaraj Surg Neurol Int Case Report BACKGROUND: Spinal cerebrospinal fluid venous fistula (CVF) is a recognized cause of chronic positional headache and spontaneous intracranial hypotension (SIH). It occurs due to an aberrant connection formed between the spinal subarachnoid space and an adjacent spinal epidural vein. The diagnosis of CVF can be difficult to establish but can be documented utilizing advanced imaging techniques (e.g., enhanced MR myelography/digital subtraction myelography). Their treatment involves surgical ligation of the involved nerve root, imaging-guided epidural blood patching, and/or endovascular embolization. Here, we report a 40-year-old male who presented with a symptomatic lumbar CVF successfully treated with transvenous embolization. CASE DESCRIPTION: A 40-year-old male presented with several months of positional headaches. The MRI of the brain showed diffuse pachymeningeal enhancement consistent with the diagnosis of SIH. Although the MR of the lumbar spine was unremarkable, the MR myelogram with digital subtraction imaging showed a CVF at the L2 level. Following transvenous embolization (i.e., through the Azygous vein), the patient’s symptoms fully resolved. CONCLUSION: Spinal CVF are rare and may cause chronic headaches and symptoms/signs of SIH. In this case, an MR myelogram with digital subtraction images demonstrated the anomalous connection between the spinal subarachnoid space and an adjacent spinal epidural vein at the L2 level. Although open surgical ablation of this connection may be feasible, less invasive techniques such as endovascular embolization should become the treatment of choice for the future management of CVF. Scientific Scholar 2021-09-30 /pmc/articles/PMC8571307/ /pubmed/34754542 http://dx.doi.org/10.25259/SNI_878_2021 Text en Copyright: © 2021 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Aljuboori, Zaid
McGrath, Margaret
Essibayi, Muhammed Amir
Zaidi, Saif
Hallam, Danial
Ghodke, Basavaraj
Spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: A case report
title Spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: A case report
title_full Spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: A case report
title_fullStr Spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: A case report
title_full_unstemmed Spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: A case report
title_short Spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: A case report
title_sort spontaneous spinal cerebrospinal fluid venous-fistula treated with transvenous embolization: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571307/
https://www.ncbi.nlm.nih.gov/pubmed/34754542
http://dx.doi.org/10.25259/SNI_878_2021
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