Calabria Ferdinando, Chiaravalloti Agostino, Cicciò Carmelo, Gangemi Vincenzo, Gullà Domenico, Rocca Federico, Gallo Gianpasquale, Cascini Giuseppe Lucio, Schillaci Orazio
Neuroimaging PET/MRI Research Unit, Institute of Molecular Bioimaging and Physiology, Italian National Research Council, IBFM-CNR, Catanzaro, Italy.
Department of Diagnostic and Molecular Imaging, Interventional Radiology and Radiotherapy, University Hospital "Tor Vergata", Rome, Italy.
Nucl Med Biol. 2017 Aug;51:40-54. doi: 10.1016/j.nucmedbio.2017.04.004. Epub 2017 Apr 17.
The C/F-choline is a PET/CT radiopharmaceutical useful in detecting tumors with high lipogenesis. C/F-choline uptake can occur in physiological conditions or tumors. The knowledge of its bio-distribution is essential to recognize physiologic variants or diagnostic pitfalls. Moreover, few information are available on the bio-distribution of this tracer in female patients. Our aim was to discuss some documented F-choline PET/CT pitfalls in prostate cancer patients. Our secondary aim was to describe the F-choline bio-distribution in the female body.
We collected diagnostic pitfalls in three PET centers examining 1000 prostate cancer by F-choline PET/CT. All pitfalls were ensured by follow-up, imaging and/or histology. We also performed whole body F-choline PET/CT in 5 female patients.
169/1000 (16.9%) patients showed pitfalls not owing to prostate cancer. These findings were due to inflammation, benign tumors while, in 1% of examined patients, a concomitant neoplasm was found. In the female body, the breast showed low physiological uptake.
The accurate knowledge of F-choline PET/CT bio-distribution and diagnostic pitfalls is essential. Correlative imaging and histological exam are often necessary to depict pitfalls. In women, the uptake in the breast is due to the physiological gradient of F-choline uptake in the exocrine glands.
Our results confirm the possibility of F-choline uptake in several diseases other than prostate cancer. However, our experience was acquired on a large population and shows that a conspicuous amount of F-choline diagnostic pitfalls are easily recognizable and attributable to inflammation. A new advance in knowledge is the minimal difference in terms of physiological tracer bio-distribution between male and female patients.
The knowledge of the physiological bio-distribution and of the potential pitfalls linked of a tracer could help physicians to choose the best diagnostic and therapeutic approaches for a better patient quality of life.
C/F-胆碱是一种PET/CT放射性药物,可用于检测高脂生成的肿瘤。C/F-胆碱摄取可发生在生理状况或肿瘤中。了解其生物分布对于识别生理变异或诊断陷阱至关重要。此外,关于该示踪剂在女性患者中的生物分布的信息很少。我们的目的是讨论前列腺癌患者中一些已记录的F-胆碱PET/CT陷阱。我们的次要目的是描述F-胆碱在女性体内的生物分布。
我们收集了三个PET中心通过F-胆碱PET/CT检查1000例前列腺癌患者时出现的诊断陷阱。所有陷阱均通过随访、影像学和/或组织学得到证实。我们还对5名女性患者进行了全身F-胆碱PET/CT检查。
169/1000(16.9%)例患者显示出并非由前列腺癌引起的陷阱。这些发现归因于炎症、良性肿瘤,而在1%的受检患者中发现了合并肿瘤。在女性体内,乳腺显示出较低的生理性摄取。
准确了解F-胆碱PET/CT的生物分布和诊断陷阱至关重要。通常需要相关的影像学和组织学检查来描述陷阱。在女性中,乳腺摄取是由于外分泌腺中F-胆碱摄取的生理梯度所致。
我们的结果证实了除前列腺癌外,F-胆碱在其他几种疾病中摄取的可能性。然而,我们的经验来自大量人群,表明大量F-胆碱诊断陷阱很容易识别且可归因于炎症。知识的一项新进展是男性和女性患者在生理性示踪剂生物分布方面差异极小。
了解示踪剂的生理性生物分布以及相关的潜在陷阱,有助于医生选择最佳的诊断和治疗方法,以提高患者的生活质量。