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Quantitative MR imaging and spectroscopy of brain tumours: a step forward?

Objectives A prospective quantitative MR study of brain tumours was performed to show the potential of combining different MR techniques to distinguish various disease processes in routine clinical practice. Methods Twenty-three patients with various intracranial tumours before treatment (diagnosis...

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Published in:European radiology 2012-11, Vol.22 (11), p.2307-2318
Main Authors: Wagnerova, Dita, Herynek, Vit, Malucelli, Alberto, Dezortova, Monika, Vymazal, Josef, Urgosik, Dusan, Syrucek, Martin, Jiru, Filip, Skoch, Antonin, Bartos, Robert, Sames, Martin, Hajek, Milan
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creator Wagnerova, Dita
Herynek, Vit
Malucelli, Alberto
Dezortova, Monika
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Jiru, Filip
Skoch, Antonin
Bartos, Robert
Sames, Martin
Hajek, Milan
description Objectives A prospective quantitative MR study of brain tumours was performed to show the potential of combining different MR techniques to distinguish various disease processes in routine clinical practice. Methods Twenty-three patients with various intracranial tumours before treatment (diagnosis confirmed by a biopsy) and 59 healthy subjects were examined on a 3-T system by conventional MR imaging, 1H spectroscopic imaging, diffusion tensor imaging and T2 relaxometry. Metabolic concentrations and their ratios, T2 relaxation times and mean diffusivities were calculated and correlated on a pixel-by-pixel basis and compared to control data. Results Different tumour types and different localisations revealed specific patterns of correlations between metabolic concentrations and mean diffusivity or T2 relaxation times. The patterns distinguish given tissue states in the examined area: healthy tissue, tissue infiltrated by tumour, active tumour, oedema infiltrated by tumour, oedema, etc. This method is able to describe the complexity of a highly heterogeneous tissue in the tumour and its vicinity, and determines crucial parameters for tissue differentiation. Conclusions A combination of different MR parameters on a pixel-by-pixel basis in individual patients enables better identification of the tumour type, direction of proliferation and assessment of the tumour extension. Key Points • Magnetic resonance offers many different methods of examining the brain . • A combination of quantitative MR parameters helps distinguish different brain lesions • Different tumour types revealed specific correlation patterns amongst different MR parameters • The correlation patterns reflect highly heterogeneous complex tissue within tumours
doi_str_mv 10.1007/s00330-012-2502-6
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Methods Twenty-three patients with various intracranial tumours before treatment (diagnosis confirmed by a biopsy) and 59 healthy subjects were examined on a 3-T system by conventional MR imaging, 1H spectroscopic imaging, diffusion tensor imaging and T2 relaxometry. Metabolic concentrations and their ratios, T2 relaxation times and mean diffusivities were calculated and correlated on a pixel-by-pixel basis and compared to control data. Results Different tumour types and different localisations revealed specific patterns of correlations between metabolic concentrations and mean diffusivity or T2 relaxation times. The patterns distinguish given tissue states in the examined area: healthy tissue, tissue infiltrated by tumour, active tumour, oedema infiltrated by tumour, oedema, etc. This method is able to describe the complexity of a highly heterogeneous tissue in the tumour and its vicinity, and determines crucial parameters for tissue differentiation. Conclusions A combination of different MR parameters on a pixel-by-pixel basis in individual patients enables better identification of the tumour type, direction of proliferation and assessment of the tumour extension. Key Points • Magnetic resonance offers many different methods of examining the brain . • A combination of quantitative MR parameters helps distinguish different brain lesions • Different tumour types revealed specific correlation patterns amongst different MR parameters • The correlation patterns reflect highly heterogeneous complex tissue within tumours</description><identifier>ISSN: 0938-7994</identifier><identifier>EISSN: 1432-1084</identifier><identifier>DOI: 10.1007/s00330-012-2502-6</identifier><identifier>PMID: 22688126</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Adult ; Aged ; Biopsy ; Biopsy - methods ; Brain - pathology ; Brain cancer ; Brain Mapping - methods ; Brain Neoplasms - diagnosis ; Brain Neoplasms - pathology ; Case-Control Studies ; Diagnostic Radiology ; Diffusion ; Diffusion Tensor Imaging - methods ; Edema ; Edema - pathology ; Female ; Glioma ; Hospitals ; Humans ; Image Processing, Computer-Assisted ; Imaging ; Internal Medicine ; Interventional Radiology ; Magnetic Resonance ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Magnetic Resonance Spectroscopy - methods ; Male ; Medicine ; Medicine &amp; Public Health ; Metabolism ; Metabolites ; Middle Aged ; Neuroradiology ; Neurosurgery ; Radiology ; Spectrum analysis ; Tumors ; Ultrasound</subject><ispartof>European radiology, 2012-11, Vol.22 (11), p.2307-2318</ispartof><rights>European Society of Radiology 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-483ad9ff34562cfe06b6d9a606297332722c9a2be16ebaac8ee1a80e8ba3093d3</citedby><cites>FETCH-LOGICAL-c372t-483ad9ff34562cfe06b6d9a606297332722c9a2be16ebaac8ee1a80e8ba3093d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22688126$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wagnerova, Dita</creatorcontrib><creatorcontrib>Herynek, Vit</creatorcontrib><creatorcontrib>Malucelli, Alberto</creatorcontrib><creatorcontrib>Dezortova, Monika</creatorcontrib><creatorcontrib>Vymazal, Josef</creatorcontrib><creatorcontrib>Urgosik, Dusan</creatorcontrib><creatorcontrib>Syrucek, Martin</creatorcontrib><creatorcontrib>Jiru, Filip</creatorcontrib><creatorcontrib>Skoch, Antonin</creatorcontrib><creatorcontrib>Bartos, Robert</creatorcontrib><creatorcontrib>Sames, Martin</creatorcontrib><creatorcontrib>Hajek, Milan</creatorcontrib><title>Quantitative MR imaging and spectroscopy of brain tumours: a step forward?</title><title>European radiology</title><addtitle>Eur Radiol</addtitle><addtitle>Eur Radiol</addtitle><description>Objectives A prospective quantitative MR study of brain tumours was performed to show the potential of combining different MR techniques to distinguish various disease processes in routine clinical practice. Methods Twenty-three patients with various intracranial tumours before treatment (diagnosis confirmed by a biopsy) and 59 healthy subjects were examined on a 3-T system by conventional MR imaging, 1H spectroscopic imaging, diffusion tensor imaging and T2 relaxometry. Metabolic concentrations and their ratios, T2 relaxation times and mean diffusivities were calculated and correlated on a pixel-by-pixel basis and compared to control data. Results Different tumour types and different localisations revealed specific patterns of correlations between metabolic concentrations and mean diffusivity or T2 relaxation times. The patterns distinguish given tissue states in the examined area: healthy tissue, tissue infiltrated by tumour, active tumour, oedema infiltrated by tumour, oedema, etc. This method is able to describe the complexity of a highly heterogeneous tissue in the tumour and its vicinity, and determines crucial parameters for tissue differentiation. 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Methods Twenty-three patients with various intracranial tumours before treatment (diagnosis confirmed by a biopsy) and 59 healthy subjects were examined on a 3-T system by conventional MR imaging, 1H spectroscopic imaging, diffusion tensor imaging and T2 relaxometry. Metabolic concentrations and their ratios, T2 relaxation times and mean diffusivities were calculated and correlated on a pixel-by-pixel basis and compared to control data. Results Different tumour types and different localisations revealed specific patterns of correlations between metabolic concentrations and mean diffusivity or T2 relaxation times. The patterns distinguish given tissue states in the examined area: healthy tissue, tissue infiltrated by tumour, active tumour, oedema infiltrated by tumour, oedema, etc. This method is able to describe the complexity of a highly heterogeneous tissue in the tumour and its vicinity, and determines crucial parameters for tissue differentiation. Conclusions A combination of different MR parameters on a pixel-by-pixel basis in individual patients enables better identification of the tumour type, direction of proliferation and assessment of the tumour extension. Key Points • Magnetic resonance offers many different methods of examining the brain . • A combination of quantitative MR parameters helps distinguish different brain lesions • Different tumour types revealed specific correlation patterns amongst different MR parameters • The correlation patterns reflect highly heterogeneous complex tissue within tumours</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>22688126</pmid><doi>10.1007/s00330-012-2502-6</doi><tpages>12</tpages></addata></record>
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source Springer Nature
subjects Adult
Aged
Biopsy
Biopsy - methods
Brain - pathology
Brain cancer
Brain Mapping - methods
Brain Neoplasms - diagnosis
Brain Neoplasms - pathology
Case-Control Studies
Diagnostic Radiology
Diffusion
Diffusion Tensor Imaging - methods
Edema
Edema - pathology
Female
Glioma
Hospitals
Humans
Image Processing, Computer-Assisted
Imaging
Internal Medicine
Interventional Radiology
Magnetic Resonance
Magnetic resonance imaging
Magnetic Resonance Imaging - methods
Magnetic Resonance Spectroscopy - methods
Male
Medicine
Medicine & Public Health
Metabolism
Metabolites
Middle Aged
Neuroradiology
Neurosurgery
Radiology
Spectrum analysis
Tumors
Ultrasound
title Quantitative MR imaging and spectroscopy of brain tumours: a step forward?
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