Remote effects in the ipsilateral thalamus and/or contralateral cerebellar hemisphere using FDG PET in patients with brain tumors

Purpose To evaluate reduced metabolism in the ipsilateral thalamus (TH) and/or contralateral cerebellum (CE) according to tumor localization and cortical metabolism around the tumor in patients with brain tumors based on FDG uptake. Methods This study investigated 48 consecutive patients with solita...

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Published inJapanese journal of radiology Vol. 36; no. 4; pp. 303 - 311
Main Authors Iwasa, Hitomi, Murata, Yoriko, Nishimori, Miki, Miyatake, Kana, Tadokoro, Michiko, Kohsaki, Shino, Nogami, Munenobu, Ueba, Yusuke, Ueba, Tetsuya, Yamagami, Takuji
Format Journal Article
LanguageEnglish
Published Tokyo Springer Japan 01.04.2018
Springer Nature B.V
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Summary:Purpose To evaluate reduced metabolism in the ipsilateral thalamus (TH) and/or contralateral cerebellum (CE) according to tumor localization and cortical metabolism around the tumor in patients with brain tumors based on FDG uptake. Methods This study investigated 48 consecutive patients with solitary cerebral hemisphere parenchymal brain tumors who underwent PET/CT and MRI. Patients were divided into 4 groups (A: reduced uptake in ipsilateral TH and contralateral CE, B: reduced uptake in ipsilateral TH only, C: reduced uptake in contralateral CE only, and D: no reduced uptake in ipsilateral TH or contralateral CE). FDG uptake and MRI findings were compared among these groups. Results Of 48 patients, group A included 24 (50%), group B included 10 (21%), group C included 0, and group D included 14 (29%). No significant tendencies were observed between the groups regarding tumor localization. However, reduced cortical metabolism around the tumor was observed in 22 patients in group A, 7 patients in group B, and 1 patient in group D. All patients in group B showed reduced metabolism from around the tumor up to the ipsilateral TH. Conclusion Reduced FDG uptake in ipsilateral TH and contralateral CE usually occur simultaneously in patients with solitary brain tumors.
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ISSN:1867-1071
1867-108X
DOI:10.1007/s11604-018-0721-8