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Visualization of the medial forebrain bundle using diffusion tensor imaging

Diffusion tensor imaging is a technique that enables physicians the portrayal of white matter tracts in vivo. We used this technique in order to depict the medial forebrain bundle (MFB) in 15 consecutive patients between 2012 and 2015. Men and women of all ages were included. There were six women an...

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Autores principales: Hana, Ardian, Hana, Anisa, Dooms, Georges, Boecher-Schwarz, Hans, Hertel, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628102/
https://www.ncbi.nlm.nih.gov/pubmed/26581828
http://dx.doi.org/10.3389/fnana.2015.00139
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author Hana, Ardian
Hana, Anisa
Dooms, Georges
Boecher-Schwarz, Hans
Hertel, Frank
author_facet Hana, Ardian
Hana, Anisa
Dooms, Georges
Boecher-Schwarz, Hans
Hertel, Frank
author_sort Hana, Ardian
collection PubMed
description Diffusion tensor imaging is a technique that enables physicians the portrayal of white matter tracts in vivo. We used this technique in order to depict the medial forebrain bundle (MFB) in 15 consecutive patients between 2012 and 2015. Men and women of all ages were included. There were six women and nine men. The mean age was 58.6 years (39–77). Nine patients were candidates for an eventual deep brain stimulation. Eight of them suffered from Parkinson‘s disease and one had multiple sclerosis. The remaining six patients suffered from different lesions which were situated in the frontal lobe. These were 2 metastasis, 2 meningiomas, 1 cerebral bleeding, and 1 glioblastoma. We used a 3DT1-sequence for the navigation. Furthermore T2- and DTI- sequences were performed. The FOV was 200 × 200 mm(2), slice thickness 2 mm, and an acquisition matrix of 96 × 96 yielding nearly isotropic voxels of 2 × 2 × 2 mm. 3-Tesla-MRI was carried out strictly axial using 32 gradient directions and one b0-image. We used Echo-Planar-Imaging (EPI) and ASSET parallel imaging with an acceleration factor of 2. b-value was 800 s/mm(2). The maximal angle was 50°. Additional scanning time was < 9 min. We were able to visualize the MFB in 12 of our patients bilaterally and in the remaining three patients we depicted the MFB on one side. It was the contralateral side of the lesion. These were 2 meningiomas and one metastasis. Portrayal of the MFB is possible for everyday routine for neurosurgical interventions. As part of the reward circuitry it might be of substantial importance for neurosurgeons during deep brain stimulation in patients with psychiatric disorders. Surgery in this part of the brain should always take the preservation of this white matter tract into account.
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spelling pubmed-46281022015-11-18 Visualization of the medial forebrain bundle using diffusion tensor imaging Hana, Ardian Hana, Anisa Dooms, Georges Boecher-Schwarz, Hans Hertel, Frank Front Neuroanat Neuroscience Diffusion tensor imaging is a technique that enables physicians the portrayal of white matter tracts in vivo. We used this technique in order to depict the medial forebrain bundle (MFB) in 15 consecutive patients between 2012 and 2015. Men and women of all ages were included. There were six women and nine men. The mean age was 58.6 years (39–77). Nine patients were candidates for an eventual deep brain stimulation. Eight of them suffered from Parkinson‘s disease and one had multiple sclerosis. The remaining six patients suffered from different lesions which were situated in the frontal lobe. These were 2 metastasis, 2 meningiomas, 1 cerebral bleeding, and 1 glioblastoma. We used a 3DT1-sequence for the navigation. Furthermore T2- and DTI- sequences were performed. The FOV was 200 × 200 mm(2), slice thickness 2 mm, and an acquisition matrix of 96 × 96 yielding nearly isotropic voxels of 2 × 2 × 2 mm. 3-Tesla-MRI was carried out strictly axial using 32 gradient directions and one b0-image. We used Echo-Planar-Imaging (EPI) and ASSET parallel imaging with an acceleration factor of 2. b-value was 800 s/mm(2). The maximal angle was 50°. Additional scanning time was < 9 min. We were able to visualize the MFB in 12 of our patients bilaterally and in the remaining three patients we depicted the MFB on one side. It was the contralateral side of the lesion. These were 2 meningiomas and one metastasis. Portrayal of the MFB is possible for everyday routine for neurosurgical interventions. As part of the reward circuitry it might be of substantial importance for neurosurgeons during deep brain stimulation in patients with psychiatric disorders. Surgery in this part of the brain should always take the preservation of this white matter tract into account. Frontiers Media S.A. 2015-10-31 /pmc/articles/PMC4628102/ /pubmed/26581828 http://dx.doi.org/10.3389/fnana.2015.00139 Text en Copyright © 2015 Hana, Hana, Dooms, Boecher-Schwarz and Hertel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Hana, Ardian
Hana, Anisa
Dooms, Georges
Boecher-Schwarz, Hans
Hertel, Frank
Visualization of the medial forebrain bundle using diffusion tensor imaging
title Visualization of the medial forebrain bundle using diffusion tensor imaging
title_full Visualization of the medial forebrain bundle using diffusion tensor imaging
title_fullStr Visualization of the medial forebrain bundle using diffusion tensor imaging
title_full_unstemmed Visualization of the medial forebrain bundle using diffusion tensor imaging
title_short Visualization of the medial forebrain bundle using diffusion tensor imaging
title_sort visualization of the medial forebrain bundle using diffusion tensor imaging
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628102/
https://www.ncbi.nlm.nih.gov/pubmed/26581828
http://dx.doi.org/10.3389/fnana.2015.00139
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