Pitfalls in integrated CT-PET of the thorax: Implications in oncologic imaging

被引:21
作者
Truong, Mylene T.
Pan, Tinsu
Erasmus, Jeremy J.
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Diagnost Radiol, Unit 57, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Imaging Phys, Houston, TX 77030 USA
关键词
positron emission tomography; computed tomography; thorax; malignancy;
D O I
10.1097/00005382-200605000-00003
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Integrated computed tomography-positron emission tomography (CT-PET) scanners improve localization of regions of increased [18F]-fluoro-2-deoxy-D-glucose (FDG) uptake and staging accuracy by allowing the near-simultaneous acquisition of coregistered, spatially matched functional and morphologic data in the same examination. However, many benign lesions can accumulate FDG and be potential pitfalls in interpretation. With the increased use of CT-PET in oncologic imaging, misinterpretation of these potential pitfalls can have significant clinical ramifications and alter staging and management. In this article, we review the physiologic uptake of FDG, normal variants, and potential pitfalls in the integrated CT-PET imaging of the thorax and their implications in oncologic imaging.
引用
收藏
页码:111 / 122
页数:12
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