于彤,朱家瑞,许根祥.病灶靶/本底比值随时间的变化规律观察[J].中国医学影像技术,2008,24(1):134~136
病灶靶/本底比值随时间的变化规律观察
Variation of lesion/background ratios with time in
malignant and benign tumor
投稿时间:2007-07-04  修订日期:2007-11-21
DOI:
中文关键词:  符合线路(SPECT/CT)  脱氧葡萄糖  双时相显像  靶/本底比值
英文关键词:SPECT/CT  Deoxyglucose  Dualtime point imaging  Lesion/Background ratios
基金项目:
作者单位E-mail
于彤 海军总医院核医学科,北京 100037 tong71@hotmail.com 
朱家瑞 海军总医院核医学科,北京 100037  
许根祥 海军总医院核医学科,北京 100037  
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中文摘要:
      目的 回顾性分析符合线路 (SPECT/CT)显像,观察良性病灶和恶性病灶18F-FDG摄取随时间的变化规律,指导合理选择FDG显像时段。方法 对160人次的(男112人次,女48人次)的262个病灶(恶性176个,良性86个)FDG肿瘤显像的图像进行回顾性分析。病人无糖尿病病史,空腹血糖正常,禁食6小时以上,静脉注射18F-FDG 5.0~10.32 mCi (185~381.84 MBq),平均为(7.5±1.40) mCi (227.5 MBq)后使用多功能ECT MillenniunTMVG8+Hawkeye (SPECT/CT)进行2D图像采集。最早显像时间为66 min,最晚为399 min(其中有一部分选择的是延时显像数据)。每人采集1~3个床位,每床位40 cm。用CT数据进行衰减校正,使用OSEM法进行图像重建。结果 分析病灶靶/本底比值时间曲线:①注药后的120~180 min,良恶性病灶的靶/本底比值差别最显著。此时为鉴别良恶性病灶的最佳显像时间。②双时相采集可以根据实际情况选择:①注药后30 min时进行第一时相图像采集,90 min进行第二时相的图像采集。此时,良性病灶的靶/本底比值降低,恶性病灶为初始上升期。有利于良性病灶的排除。②第一时相注药后的60~120 min内进行,第2时相在注药后的120~180 min内进行,有利于鉴别恶性病灶(此时良性病灶为平台期、缓慢上升或下降期),恶性病灶为上升期。3 必要时可进行3时相显像,通过三个时间点病灶摄取值的特点,鉴别病灶的性质。理论上会提高FDG的鉴别诊断价值。结论 准确掌握不同性质病灶的FDG代谢时间曲线,利用多时相显像技术可以更好利用和提高FDG肿瘤显像的价值。
英文摘要:
      Objective To understand the Lesion/Background Ratio(L/B) varying with time in malignant and benign tissues the SPECT/CT images were analyzed retrospectively. It will benefit us to acquire whole body scan at appropriate time point. Methods The study population consisted of 160 patients(male: 112, female: 48)with 262 lesions(malignant: 176,benign:86).The patients were administrated 5.0-10.32 mCi (185-381.84 MBq) 18F-FDG by intravenous injection. Images were acquired (2-3 beds) with multifunction ECT MillenniunTMVG8+Hawkeye (SPECT/CT) afte injection in 2D mode, reconstructed using the method of OSEM (21 subsets, twice iterations). The final diagnoses of these patients were proven either by histopathology or by biopsy,or by a clinical and radiographic follow-up.The statistical analysis of quantitatie data were performed by SPSS 13.0. Results The L/B ratio of benign tissues falled down to its lowest point at 120-180 min after injection, and achieved its peak again at 180-240 min (the first peak was estimated at about 30 min after injection). While, malignant tumor showed a greater rise of L/B until it achieved the peak at 240-300 min after injection. Synthesising and analysising the trend lines which we got in this study and some predecessor’s findings, we have a conclusion that, besides the well known method(i.e. the first phase image aquired at 60-120 min and delayed phase image at 120-180 min after injection)which show us the L/B ratio rising of malignant lesions, dualtime point 18F-FDG imaging can also be aquired at 30 min and 90 min, alternativly. And what different it from the above is that it show us the falling down of L/B ratio of the benign tusses. IF necessary, we can use three time point imaging to improve the diagnosis accuracy.The trend line also show that it is at 120-180 min after injection when L/B ratio achieves its stronger contrast. Conclusion Understanding the metabolism rule of the malignant lesions and benign lesions well benefit us to select the optimal scan time or multi-phase techniques in order to improve the diagnosis value of FDG SPECT/CT tumor imagings.
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