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An isolated ruptured spinal aneurysm presents with a thalamic Infarct: case report

BACKGROUND: Isolated spinal artery aneurysms are extremely rare, and their pathogenesis, clinical presentation, and treatment strategies are poorly established. We report only the second case of a patient with an isolated posterior spinal aneurysm and concurrent left thalamic infarct and review the...

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Autores principales: Tenorio, Alexander, Holmes, Brandon B., Abla, Adib A., Amans, Matthew, Meisel, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856767/
https://www.ncbi.nlm.nih.gov/pubmed/33535981
http://dx.doi.org/10.1186/s12883-021-02055-5
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author Tenorio, Alexander
Holmes, Brandon B.
Abla, Adib A.
Amans, Matthew
Meisel, Karl
author_facet Tenorio, Alexander
Holmes, Brandon B.
Abla, Adib A.
Amans, Matthew
Meisel, Karl
author_sort Tenorio, Alexander
collection PubMed
description BACKGROUND: Isolated spinal artery aneurysms are extremely rare, and their pathogenesis, clinical presentation, and treatment strategies are poorly established. We report only the second case of a patient with an isolated posterior spinal aneurysm and concurrent left thalamic infarct and review the literature to help clarify treatment strategies of isolated spinal aneurysms. CASE PRESENTATION: A 49-year-old patient presented with acute onset walking difficulty followed by diaphoresis, back and abdominal pain, and paraplegia. Imaging was notable for a hemorrhagic spinal lesion with compression at T12 through L4 and an acute left thalamic infarct. Surgical exploration revealed an isolated posterior spinal artery aneurysm. The aneurysm was surgically resected and the patient had partial recovery six months post-operatively. CONCLUSIONS: Isolated posterior spinal artery aneurysms of the thoracolumbar region are rare lesions that commonly present with abdominal pain, radiating back pain, and lower extremity weakness. Imaging may not provide a definitive diagnosis. The three primary treatment strategies are conservative management, endovascular treatment, or surgical resection. In patients with symptomatic cord compression, immediate surgical intervention is indicated to preserve neurologic function. In all other cases, the artery size, distal flow, morphology, and location may guide management.
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spelling pubmed-78567672021-02-04 An isolated ruptured spinal aneurysm presents with a thalamic Infarct: case report Tenorio, Alexander Holmes, Brandon B. Abla, Adib A. Amans, Matthew Meisel, Karl BMC Neurol Case Report BACKGROUND: Isolated spinal artery aneurysms are extremely rare, and their pathogenesis, clinical presentation, and treatment strategies are poorly established. We report only the second case of a patient with an isolated posterior spinal aneurysm and concurrent left thalamic infarct and review the literature to help clarify treatment strategies of isolated spinal aneurysms. CASE PRESENTATION: A 49-year-old patient presented with acute onset walking difficulty followed by diaphoresis, back and abdominal pain, and paraplegia. Imaging was notable for a hemorrhagic spinal lesion with compression at T12 through L4 and an acute left thalamic infarct. Surgical exploration revealed an isolated posterior spinal artery aneurysm. The aneurysm was surgically resected and the patient had partial recovery six months post-operatively. CONCLUSIONS: Isolated posterior spinal artery aneurysms of the thoracolumbar region are rare lesions that commonly present with abdominal pain, radiating back pain, and lower extremity weakness. Imaging may not provide a definitive diagnosis. The three primary treatment strategies are conservative management, endovascular treatment, or surgical resection. In patients with symptomatic cord compression, immediate surgical intervention is indicated to preserve neurologic function. In all other cases, the artery size, distal flow, morphology, and location may guide management. BioMed Central 2021-02-03 /pmc/articles/PMC7856767/ /pubmed/33535981 http://dx.doi.org/10.1186/s12883-021-02055-5 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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
Tenorio, Alexander
Holmes, Brandon B.
Abla, Adib A.
Amans, Matthew
Meisel, Karl
An isolated ruptured spinal aneurysm presents with a thalamic Infarct: case report
title An isolated ruptured spinal aneurysm presents with a thalamic Infarct: case report
title_full An isolated ruptured spinal aneurysm presents with a thalamic Infarct: case report
title_fullStr An isolated ruptured spinal aneurysm presents with a thalamic Infarct: case report
title_full_unstemmed An isolated ruptured spinal aneurysm presents with a thalamic Infarct: case report
title_short An isolated ruptured spinal aneurysm presents with a thalamic Infarct: case report
title_sort isolated ruptured spinal aneurysm presents with a thalamic infarct: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856767/
https://www.ncbi.nlm.nih.gov/pubmed/33535981
http://dx.doi.org/10.1186/s12883-021-02055-5
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