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PET imaging in testicular tumours
被引:6
|作者:
Calabro, Dlletta
[1
]
Telo, Silvi
[1
]
Ambrosini, Valentina
[1
]
机构:
[1] DIMES Univ Bologna, S Orsola Malpighi Hosp, Nucl Med, Bologna, Italy
关键词:
18F-fluorodeoxyglucose;
germ-cells tumours;
nonseminoma;
PET;
computed tomography;
seminoma;
testicular cancer;
POSITRON-EMISSION-TOMOGRAPHY;
POSTCHEMOTHERAPY SEMINOMA;
CONSENSUS CONFERENCE;
F-18-FDG PET/CT;
CELL TUMOR;
CANCER;
DIAGNOSIS;
GRANULOMATOSIS;
GUIDELINES;
LESIONS;
D O I:
10.1097/MOU.0000000000000796
中图分类号:
R5 [内科学];
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号:
1002 ;
100201 ;
摘要:
Purpose of review Testicular cancer is rare, but its incidence is expected to rise. [18F] fluorodeoxyglucose ([18F]FDG) PET/computed tomography (CT) added role in testicular cancer management has been defined in a set of specific clinical settings. The current review focuses on recent advances in the employment of PET/CT in testicular cancer patients. Recent findings [18F]FDG PET/CT is not recommended for initial staging or for suspected testicular tumours. PET/CT role in testicular cancer management is mainly for the assessment of seminoma residual masses after therapy (>3 cm). Although [18F]FDG PET/CT has a very high negative predictive value, its positive predictive value varies across studies: appropriate PET/CT scheduling after therapy and a careful history are mandatory for accurate interpretation. Interim PET/CT could prove valuable to spare subsequent chemotherapy cycles in patients already in remission, reducing related toxicity. The role of [18F]FDG in nonseminoma tumours is hampered by the low sensitivity in teratoma. [18F]FDG PET/CT is currently used for the assessment of seminoma residual masses (>3 cm) after therapy. A negative PET could also spare unnecessary further chemotherapy cycles in responding patients, reducing toxicity. Although rare, testicular secondary lesions can be detected with non[18F]FDG tracers when PET/CT is performed for other primary tumours.
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页码:665 / 671
页数:7
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