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Verfasst von:Radbruch, Alexander [VerfasserIn]   i
 Wiestler, Benedikt [VerfasserIn]   i
 Kramp, Linda Katharina [VerfasserIn]   i
 Lutz, Kira [VerfasserIn]   i
 Bäumer, Philipp [VerfasserIn]   i
 Weiler, Markus [VerfasserIn]   i
 Röthke, Matthias C. [VerfasserIn]   i
 Sahm, Felix [VerfasserIn]   i
 Schlemmer, Heinz-Peter [VerfasserIn]   i
 Wick, Wolfgang [VerfasserIn]   i
 Heiland, Sabine [VerfasserIn]   i
 Bendszus, Martin [VerfasserIn]   i
Titel:Differentiation of glioblastoma and primary CNS lymphomas using susceptibility weighted imaging
Verf.angabe:Alexander Radbruch, Benedikt Wiestler, Linda Kramp, Kira Lutz, Philipp Bäumer, Markus Weiler, Matthias Roethke, Felix Sahm, Heinz-Peter Schlemmer, Wolfgang Wick, Sabine Heiland, Martin Bendszus
E-Jahr:2013
Jahr:March 2013
Umfang:5 S.
Fussnoten:Published online: December 12, 2012 ; Gesehen am 28.11.2018
Titel Quelle:Enthalten in: European journal of radiology
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1990
Jahr Quelle:2013
Band/Heft Quelle:82(2013), 3, Seite 552-556
ISSN Quelle:1872-7727
Abstract:Introduction Reliable differentiation between glioblastoma and primary CNS lymphoma (PCNSL) using conventional MR imaging is challenging, since both entities may show similar appearance on structural MR imaging. Here we analyzed if the appearance of intratumoural susceptibility signals (ITSS) on susceptibility weighted imaging (SWI) may differentiate between both entities. Methods and materials SWI and contrast enhanced T1-weighted images were acquired from 15 patients with newly diagnosed PCNSL (14 B-cell PCNSL, 1 T-cell PCNSL) and 117 patients with newly diagnosed glioblastoma with a 3 Tesla MR. Additional phase images were available in 8 patients with PCNSL and 88 patients with glioblastoma. Appearance of ITSS was assessed by two readers on SWI and the size of the enhancing lesions on contrast enhanced T1-weighted images were measured. Furthermore it was assessed if ITSS displayed more clearly on SWI or on phase images. Results ITSS were detected in 106 (reader 1) and 109 (reader 2) glioblastoma, respectively. Both readers identified ITSS within the T-cell PCNSL while both readers did not identify any ITSS within the 14 Bcell PCNSL. Interrarter variability as determined by Cohen κ was excellent for glioblastoma (κ = 0.938) and for PCNSL (κ = 1). The medium size of the enhancing lesion of the glioblastoma that did not harbour ITSS was significantly smaller than the size of the glioblastoma exhibiting ITSS (p < 0.008). All identified ITSS displayed more clearly on SWI than on phase images. Conclusion Presence of ITSS differentiates reliably between glioblastoma and B-cell PCNSL and provides a fast bases for the clinical decision without causing any postprocessing work.
DOI:doi:10.1016/j.ejrad.2012.11.002
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: http://dx.doi.org/10.1016/j.ejrad.2012.11.002
 Volltext: https://www.ejradiology.com/article/S0720-048X(12)00542-6/abstract
 DOI: https://doi.org/10.1016/j.ejrad.2012.11.002
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:FLAIR
 fluid attenuated inversion recovery
 Glioblastoma
 intratumoural susceptibility signals
 Intratumoural susceptibility signals
 ITSS
 PCNSL
 primary central nervous system lymphoma
 Primary CNS lymphoma
 Susceptibility weighted imaging
K10plus-PPN:1584606959
Verknüpfungen:→ Zeitschrift

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