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   <subfield code="a">10.1007/s11547-012-0801-5</subfield>
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   <subfield code="a">Comparison between CT and MR in perfusion imaging assessment of high-grade gliomas</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[M. De Simone, C. Muccio, S. Pagnotta, G. Esposito, A. Cianfoni]</subfield>
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   <subfield code="a">Confronto tra studio di perfusione con metodica RM e con metodica TC nei gliomi cerebrali di alto grado</subfield>
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   <subfield code="a">Purpose: The aim of our study was to compare the relative cerebral blood volume (CBV) values obtained by first-pass dynamic susceptibility-weighted contrast-enhanced (DSC) T2-weighted magnetic resonance (MR) and perfusion computed tomography (P-CT) imaging in high-grade gliomas (HGG) in the same patient population. Materials and methods: Sixteen patients with histologically proven HGG underwent P-CT and DSC-MR brain imaging. P-CT studies were obtained using a four-row multislice CT scanner and postprocessed with a commercial software package based on a deconvolution-based technique. DSC-MR images were obtained at 1.5 T with a first-pass dynamic susceptibility contrast-enhanced T2-weighted sequence. P-CT and DSC-MR images were obtained within 4 days of each another, always before surgery. Maximum CBV ratios normalised with contralateral white matter (rCBV) were calculated. Statistical analysis was performed with the classical parametric statistic procedure. Results: A linear correlation between maximum rCBV values obtained with P-CT and DSC-MR imaging was evident. The best linear model is CT=slope×MR+error and provides a highly significant estimate of the slope equal to 1.08. Thus CT results can be predicted from MR values. Therefore, it is also possible to predict MR results from CT values by estimating the linear model MR=slope×CT+error. DSC-MR imaging gave lower rCBV average values (4.92±1.52) compared with P-CT (5.56±1.55). Conclusions: In our population of patients, P-CT and DSC-MR imaging showed proportional results in rCBV assessment of HGGs, and thus both modalities may be used interchangeably in HGG of the brain.</subfield>
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   <subfield code="a">Springer-Verlag Italia, 2012</subfield>
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   <subfield code="a">Dynamic-susceptibility contrast-enhanced MR imaging</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Perfusion CT</subfield>
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   <subfield code="a">High grade glioma</subfield>
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   <subfield code="a">T1 effect</subfield>
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   <subfield code="a">Dynamic susceptibility contrast enhanced MR imaging</subfield>
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   <subfield code="a">TC perfusione</subfield>
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   <subfield code="a">Gliomi di alto grado</subfield>
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   <subfield code="a">Effetto T1</subfield>
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   <subfield code="a">De Simone</subfield>
   <subfield code="D">M.</subfield>
   <subfield code="u">UOC Neuroradiologia, Dipartimento di Neuroscienze, AORN &quot;G. Rummo”, Via dell'Angelo 1, 82100, Benevento, Italy</subfield>
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   <subfield code="a">Muccio</subfield>
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   <subfield code="u">UOC Neuroradiologia, Dipartimento di Neuroscienze, AORN &quot;G. Rummo”, Via dell'Angelo 1, 82100, Benevento, Italy</subfield>
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   <subfield code="u">Dipartimento di Statistica, Università degli Studi del Sannio, Benevento, Italy</subfield>
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   <subfield code="a">Esposito</subfield>
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   <subfield code="u">Radiology Department, Medical University South Carolina (MUSC), Charleston, SC, USA</subfield>
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   <subfield code="t">La radiologia medica</subfield>
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