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Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report

BACKGROUND: Gadolinium enhancement of spinal nerve roots on magnetic resonance imaging (MRI) has rarely been reported in spinal dural arteriovenous fistula (SDAVF). Nerve root enhancement and cerebrospinal fluid (CSF) pleocytosis can be deceptive and lead to a misdiagnosis of myeloradiculitis. We re...

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Autores principales: Chiang, Sharon, Pet, Douglas B., Talbott, Jason F., LaHue, Sara C., Douglas, Vanja C., Rosendale, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903490/
https://www.ncbi.nlm.nih.gov/pubmed/36750779
http://dx.doi.org/10.1186/s12883-023-03097-7
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author Chiang, Sharon
Pet, Douglas B.
Talbott, Jason F.
LaHue, Sara C.
Douglas, Vanja C.
Rosendale, Nicole
author_facet Chiang, Sharon
Pet, Douglas B.
Talbott, Jason F.
LaHue, Sara C.
Douglas, Vanja C.
Rosendale, Nicole
author_sort Chiang, Sharon
collection PubMed
description BACKGROUND: Gadolinium enhancement of spinal nerve roots on magnetic resonance imaging (MRI) has rarely been reported in spinal dural arteriovenous fistula (SDAVF). Nerve root enhancement and cerebrospinal fluid (CSF) pleocytosis can be deceptive and lead to a misdiagnosis of myeloradiculitis. We report a patient who was initially diagnosed with neurosarcoid myeloradiculitis due to spinal nerve root enhancement, mildly inflammatory cerebrospinal fluid, and pulmonary granulomas, who ultimately was found to have an extensive symptomatic SDAVF. CASE PRESENTATION: A 52-year-old woman presented with a longitudinally extensive spinal cord lesion with associated gadolinium enhancement of the cord and cauda equina nerve roots, and mild lymphocytic pleocytosis. Pulmonary lymph node biopsy revealed non-caseating granulomas and neurosarcoid myeloradiculitis was suspected. She had rapid and profound clinical deterioration after a single dose of steroids. Further work-up with spinal angiography revealed a thoracic SDAVF, which was surgically ligated leading to clinical improvement. CONCLUSIONS: This case highlights an unexpected presentation of SDAVF with nerve root enhancement and concurrent pulmonary non-caseating granulomas, leading to an initial misdiagnosis with neurosarcoidosis. Nerve root enhancement has only rarely been described in cases of SDAVF; however, as this case highlights, it is an important consideration in the differential diagnosis of non-inflammatory causes of longitudinally extensive myeloradiculopathy with nerve root enhancement. This point is highly salient due to the importance of avoiding misdiagnosis of SDAVF, as interventions such as steroids or epidural injections used to treat inflammatory or infiltrative mimics may worsen symptoms in SDAVF. We review the presentation, diagnosis, and management of SDAVF as well as a proposed diagnostic approach to differentiating SDAVF from inflammatory myeloradiculitis.
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spelling pubmed-99034902023-02-08 Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report Chiang, Sharon Pet, Douglas B. Talbott, Jason F. LaHue, Sara C. Douglas, Vanja C. Rosendale, Nicole BMC Neurol Case Report BACKGROUND: Gadolinium enhancement of spinal nerve roots on magnetic resonance imaging (MRI) has rarely been reported in spinal dural arteriovenous fistula (SDAVF). Nerve root enhancement and cerebrospinal fluid (CSF) pleocytosis can be deceptive and lead to a misdiagnosis of myeloradiculitis. We report a patient who was initially diagnosed with neurosarcoid myeloradiculitis due to spinal nerve root enhancement, mildly inflammatory cerebrospinal fluid, and pulmonary granulomas, who ultimately was found to have an extensive symptomatic SDAVF. CASE PRESENTATION: A 52-year-old woman presented with a longitudinally extensive spinal cord lesion with associated gadolinium enhancement of the cord and cauda equina nerve roots, and mild lymphocytic pleocytosis. Pulmonary lymph node biopsy revealed non-caseating granulomas and neurosarcoid myeloradiculitis was suspected. She had rapid and profound clinical deterioration after a single dose of steroids. Further work-up with spinal angiography revealed a thoracic SDAVF, which was surgically ligated leading to clinical improvement. CONCLUSIONS: This case highlights an unexpected presentation of SDAVF with nerve root enhancement and concurrent pulmonary non-caseating granulomas, leading to an initial misdiagnosis with neurosarcoidosis. Nerve root enhancement has only rarely been described in cases of SDAVF; however, as this case highlights, it is an important consideration in the differential diagnosis of non-inflammatory causes of longitudinally extensive myeloradiculopathy with nerve root enhancement. This point is highly salient due to the importance of avoiding misdiagnosis of SDAVF, as interventions such as steroids or epidural injections used to treat inflammatory or infiltrative mimics may worsen symptoms in SDAVF. We review the presentation, diagnosis, and management of SDAVF as well as a proposed diagnostic approach to differentiating SDAVF from inflammatory myeloradiculitis. BioMed Central 2023-02-07 /pmc/articles/PMC9903490/ /pubmed/36750779 http://dx.doi.org/10.1186/s12883-023-03097-7 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
Chiang, Sharon
Pet, Douglas B.
Talbott, Jason F.
LaHue, Sara C.
Douglas, Vanja C.
Rosendale, Nicole
Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report
title Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report
title_full Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report
title_fullStr Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report
title_full_unstemmed Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report
title_short Spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report
title_sort spinal epidural arteriovenous fistula with nerve root enhancement mimicking myeloradiculitis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903490/
https://www.ncbi.nlm.nih.gov/pubmed/36750779
http://dx.doi.org/10.1186/s12883-023-03097-7
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