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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1998-6-8
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pubmed:abstractText |
Management of low-grade gliomas continues to be a challenging task, because CT and MRI do not always differentiate from nontumoral lesions. Furthermore, tumor extent and aggressiveness often remain unclear because of a lack of contrast enhancement. Previous studies indicated that large neutral amino acid tracers accumulate in most brain tumors, including low-grade gliomas, probably because of changes of endothelial and blood-brain barrier function. We describe 11C-methionine uptake measured with PET in a series of 196 consecutive patients, most of whom were studied because of suspected low-grade gliomas. Uptake in the most active lesion area, relative to contralateral side, was significantly different among high-grade gliomas, low-grade gliomas, and chronic or subacute nontumoral lesions, and this difference was independent from contrast enhancement in CT or MRI. Corticosteroids had no significant effect on methionine uptake in low-grade gliomas but reduced uptake moderately in high-grade gliomas. Differentiation between gliomas and nontumoral lesions by a simple threshold was correct in 79%. Recurrent or residual tumors had a higher uptake than primary gliomas. In conclusion, the high sensitivity of 11C-methionine uptake for functional endothelial or blood-brain barrier changes suggests that this tracer is particularly useful for evaluation and follow-up of low-grade gliomas.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0028-3878
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pubmed:author |
pubmed-author:BauerBB,
pubmed-author:ErnestusR IRI,
pubmed-author:HölzerTT,
pubmed-author:HeissW DWD,
pubmed-author:HerholzKK,
pubmed-author:LöttgenJJ,
pubmed-author:MendozaGG,
pubmed-author:SchröderRR,
pubmed-author:ThielAA,
pubmed-author:VogelCC,
pubmed-author:Weber-LuxenburgerGG,
pubmed-author:WienhardKK
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pubmed:issnType |
Print
|
pubmed:volume |
50
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1316-22
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:9595980-Adult,
pubmed-meshheading:9595980-Astrocytoma,
pubmed-meshheading:9595980-Carbon Radioisotopes,
pubmed-meshheading:9595980-Diagnosis, Differential,
pubmed-meshheading:9595980-Female,
pubmed-meshheading:9595980-Glioblastoma,
pubmed-meshheading:9595980-Glioma,
pubmed-meshheading:9595980-Humans,
pubmed-meshheading:9595980-Image Enhancement,
pubmed-meshheading:9595980-Magnetic Resonance Imaging,
pubmed-meshheading:9595980-Male,
pubmed-meshheading:9595980-Methionine,
pubmed-meshheading:9595980-Middle Aged,
pubmed-meshheading:9595980-Oligodendroglioma,
pubmed-meshheading:9595980-Predictive Value of Tests,
pubmed-meshheading:9595980-Tomography, Emission-Computed,
pubmed-meshheading:9595980-Tomography, X-Ray Computed
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pubmed:year |
1998
|
pubmed:articleTitle |
11C-methionine PET for differential diagnosis of low-grade gliomas.
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pubmed:affiliation |
Klinik für Neurologie, Universität zu Köln, Germany.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Controlled Clinical Trial
|