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dc.creatorFountas, K. N.en
dc.creatorKapsalaki, E. Z.en
dc.creatorVogel, R. L.en
dc.creatorFezoulidis, I.en
dc.creatorRobinson, J. S.en
dc.creatorGotsis, E. D.en
dc.date.accessioned2015-11-23T10:26:41Z
dc.date.available2015-11-23T10:26:41Z
dc.date.issued2004
dc.identifier10.1159/000077458
dc.identifier.issn10116125
dc.identifier.urihttp://hdl.handle.net/11615/27532
dc.description.abstractBackground: Proton magnetic resonance spectroscopy (1H MRS) constitutes a promising modality to assess intracranial pathology. We present our experience using this method in grading solid brain astrocytomas. Material and Methods: Using a 1.5-Tesla MRI unit, 71 patients with the radiographic diagnosis of astrocytoma were examined. Water-suppressed single-voxel 1H MRS was employed in all of our patients. The concentrations of choline (Cho), N-acetyl-aspartate (NAA), phosphocreatine-creatine (Pcr-Cr), myo-inositol (MI), lactate (Lac), lipids (Lip) as well as the metabolite ratios of Cho/Pcr-Cr, NAA/PCr-Cr and NAA/Cho were calculated. An appropriate surgical biopsy was performed. Standard pathology examination was employed in a double-blinded fashion. Results: An increased concentration of Cho and decreased concentrations of Pcr-Cr and NAA were detected. The concentrations of Lac, Lip and MI varied inconsistently, even among tumors of the same histologic grade. The Cho/Pcr-Cr ratio was calculated. This ratio was found to be 2.15 ± 0.26 in 27 patients with astrocytomas grade I and II, 2.78 ± 0.09 in 18 patients with grade III, and 5.40 ± 0.16 in 26 patients with grade IV. Discussion: The increased concentration of Cho is due to the increased cellularity and a relatively increased number of membranous structures in highly malignant tumors. In abnormal anaerobic metabolic tumor states there is relatively less phosphorylization of creatine. By using the Cho/Pcr-Cr ratio the concomitant effects of structural and metabolic alteration can thereby be emphasized for diagnostic advantage. Conclusion: The Cho/ Pcr-Cr is a very important and statistically significant marker (p = 0.043) determining the degree of intracranial astrocytoma malignancy. Copyright © 2004 S. Karger AG, Basel.en
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-4344611566&partnerID=40&md5=8633af3f100f0766eb8228ca0e19b955
dc.subjectAstrocytomasen
dc.subjectHistologic grade, Metabolite ratioen
dc.subjectProton spectroscopy, astrocytomasen
dc.subjectbiological markeren
dc.subjectcholineen
dc.subjectcreatineen
dc.subjectcreatine phosphateen
dc.subjectinositolen
dc.subjectlactic aciden
dc.subjectlipiden
dc.subjectn acetylaspartic aciden
dc.subjectprotonen
dc.subjectwateren
dc.subjectadulten
dc.subjectageden
dc.subjectarticleen
dc.subjectastrocytomaen
dc.subjectbiopsyen
dc.subjectbrain canceren
dc.subjectcalculationen
dc.subjectcancer diagnosisen
dc.subjectconcentration (parameters)en
dc.subjectcontrolled studyen
dc.subjectfemaleen
dc.subjecthistologyen
dc.subjecthumanen
dc.subjecthuman tissueen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectpathologyen
dc.subjectproton nuclear magnetic resonanceen
dc.subjectradiodiagnosisen
dc.subjectAnalysis of Varianceen
dc.subjectBrain Neoplasmsen
dc.subjectDouble-Blind Methoden
dc.subjectHumansen
dc.subjectMagnetic Resonance Spectroscopyen
dc.subjectMiddle Ageden
dc.subjectProtonsen
dc.titleNoninvasive histologic grading of solid astrocytomas using proton magnetic resonance spectroscopyen
dc.typejournalArticleen


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