Hara Toshihiko, Kosaka Noboru, Suzuki Tsuneo, Kudo Koichiro, Niino Hitoshi
Department of Radiology, International Medical Center of Japan, Tokyo, Japan.
Chest. 2003 Sep;124(3):893-901. doi: 10.1378/chest.124.3.893.
The purpose of this study was to examine the uptake rates of (18)F-fluorodeoxyglucose (FDG) and (11)C-choline in patients with lung cancer, pulmonary tuberculosis, and atypical mycobacterial infection of the lung by positron emission tomography (PET) scanning with relation to their tumor size.
Ninety-seven patients with untreated lung cancer, 14 patients with untreated pulmonary tuberculosis, and 5 patients with untreated atypical mycobacterial infection were examined. The diagnosis of lung cancer was confirmed pathologically after biopsy and surgery. The diagnosis of tuberculosis and atypical mycobacterial infection was confirmed by bacterial culture. The uptake rates of FDG and (11)C-choline were presented quantitatively as the standardized uptake value (SUV).
International Medical Center of Japan.
In lung cancer patients, the SUV of FDG increased with increasing tumor size, whereas the SUV of (11)C-choline was almost constant at around 3.5 for every tumor size. In tuberculosis patients, the SUV of FDG increased with increasing tumor size, whereas the SUV of (11)C-choline was almost constant at around 2 for every tumor size. In atypical mycobacterial infection patients, the SUV of FDG and the SUV of (11)C-choline were equally low at around < or = 2.
The differences in the SUVs of FDG and (11)C-choline in patients with lung cancer, tuberculosis, and atypical mycobacterial infection for the same tumor size (tumor size, > 1.5 cm) were distinct. In lung cancer patients, the SUVs of both FDG and (11)C-choline were high. In tuberculosis patients, the SUV of FDG was high, but the SUV of (11)C-choline was low. In atypical mycobacterial infection patients, the SUVs of both FDG and (11)C-choline were low. It may be possible to apply this principle to make a presumptive diagnosis of a solitary pulmonary nodule if it is too small to make a definitive diagnosis pathologically and bacteriologically.
本研究旨在通过正电子发射断层扫描(PET)检查肺癌、肺结核和非典型分枝杆菌肺部感染患者中(18)F-氟脱氧葡萄糖(FDG)和(11)C-胆碱的摄取率,并探讨其与肿瘤大小的关系。
对97例未经治疗的肺癌患者、14例未经治疗的肺结核患者和5例未经治疗的非典型分枝杆菌感染患者进行检查。肺癌诊断经活检及手术后病理确诊。肺结核和非典型分枝杆菌感染诊断经细菌培养确诊。FDG和(11)C-胆碱的摄取率以标准化摄取值(SUV)定量表示。
日本国际医疗中心。
肺癌患者中,FDG的SUV随肿瘤大小增加而升高,而(11)C-胆碱的SUV在各肿瘤大小下均几乎恒定在3.5左右。肺结核患者中,FDG的SUV随肿瘤大小增加而升高,而(11)C-胆碱的SUV在各肿瘤大小下均几乎恒定在2左右。非典型分枝杆菌感染患者中,FDG的SUV和(11)C-胆碱的SUV同样较低,约≤2。
相同肿瘤大小(肿瘤大小>1.5 cm)的肺癌、肺结核和非典型分枝杆菌感染患者中,FDG和(11)C-胆碱的SUV差异明显。肺癌患者中,FDG和(11)C-胆碱的SUV均较高。肺结核患者中,FDG的SUV较高,但(11)C-胆碱的SUV较低。非典型分枝杆菌感染患者中,FDG和(11)C-胆碱的SUV均较低。对于因太小而无法进行病理和细菌学明确诊断的孤立性肺结节,应用这一原则进行初步诊断可能是可行的。