2005
DOI: 10.1586/14737140.5.6.1079
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Positron emission tomography: clinical applications in oncology. Part 1

Abstract: Positron emission tomography is a functional diagnostic imaging technique, which can accurately measure in vivo distribution of a radiopharmaceutical with high resolution. The ability of positron emission tomography to study various biologic processes opens up new possibilities for both research and day-to-day clinical use. Positron emission tomography has progressed rapidly from being a research technique in laboratories to a routine clinical imaging modality becoming part of armamentarium for the medical pro… Show more

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Cited by 33 publications
(17 citation statements)
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“…Therefore, the first aim of our study was to evaluate the biodistribution of i.a. delivered FDG is a glucose analog that accumulates in cells in a velocity that is dependent on the glycolytic rate of the cell (Gallagher et al, 1978;Kumar et al, 2005). In this study, we used FDG to monitor the effects of i.a.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, the first aim of our study was to evaluate the biodistribution of i.a. delivered FDG is a glucose analog that accumulates in cells in a velocity that is dependent on the glycolytic rate of the cell (Gallagher et al, 1978;Kumar et al, 2005). In this study, we used FDG to monitor the effects of i.a.…”
Section: Discussionmentioning
confidence: 99%
“…In general, endoscopic biopsy cannot confirm a diagnosis, because almost all benign tumors are submucosal. [ 18 F]fluoro-2-deoxy-D-glucose positron emission tomography (FDG-PET) is a powerful diagnostic modality useful for cancer staging, therapeutic monitoring, and follow-up evaluation of various malignant tumors [1,2]. Today, we often use FDG-PET to evaluate the malignant potential of detected submucosal esophageal tumors.…”
Section: Introductionmentioning
confidence: 99%
“…18 F-FDG PET/CT delineates the most metabolically active tumor regions. In particular, SUV values are useful for differentiating low-and high-grade tumors and, thus, also in differentiating benign and malignant masses, predicting tumor grade, staging and restaging, determining prognosis and identifying optimal biopsy sites [2,13,14]. Hain et al [2] found that most malignant sites, as determined by whole-tumor histology, correlated with biopsy sites identified by 18 F-FDG PET/ CT.…”
Section: Discussionmentioning
confidence: 99%
“…Hain et al [2] found that most malignant sites, as determined by whole-tumor histology, correlated with biopsy sites identified by 18 F-FDG PET/ CT. According to Kumar et al [14], 18 F-FDG PET/CT differentially delineates tumor tissues on the basis of glucose metabolism, and 18 F-FDG PET/CT imaging can be viewed as a form of metabolic biopsy [15].…”
Section: Discussionmentioning
confidence: 99%