食管癌18氟氟代脱氧葡萄糖PET/CT检查特征

Imaging characteristics of Fluorine18fluorodeoxyglucose PET/CT examination in esophageal carcinoma

  • 摘要: 【摘要】目的:总结食管癌 18氟氟代脱氧葡萄糖( 18FFDG)PET/CT检查影像学特征,以及代谢参数与分期的关系。
    方法:回顾性分析2012年1月至2014年12月第二军医大学附属长海医院收治的53例食管癌患者的临床资料。患者行全身 18FFDG PET/CT检查。分析PET/CT检查图像特征,并以SUV 25为阈值,获得食管原发病灶的最大标准摄取值(SUVmax)、平均标准摄取值(SUVavg)、肿瘤代谢体积(MTV)、最大直径,计算病灶糖酵解总量(TLG);同时测量转移区域淋巴结和远处转移癌的SUVmax。正态分布的计量资料以±s表示,组间比较采用独立样本t检验。偏态分布的计量资料以中位数M(Qn)表示,组间比较采用MannWhitney检验。
    结果:(1)肿瘤部位和体积:肿瘤位于食管颈段1例,胸上段 16例,胸中段18例,胸下段13例,同时位于胸上段+胸中段2例,胸中段+胸下段3例。肿瘤体积:16 cm×12 cm×22 cm~65 cm×70 cm×72 cm。肿瘤最大直径为(61±21)cm(25~112 cm)。(2)PET/CT检查表现:食管原发病灶:962%(51/53)的患者食管局限性 18FFDG摄取值增高,伴管壁增厚;病灶与正常食管壁分界不清;病变段管腔狭窄。38%(2/53)的患者食管局部结节样 18FFDG摄取值增高,CT检查图像示管壁未见增厚。邻近结构:245%(13/53)的患者肿瘤侵犯周围组织器官。受侵犯组织器官 18FFDG摄取值增高,与食管原发病灶分界不清。区域淋巴结:774%(41/53)的患者发生区域淋巴结转移。转移淋巴结 18FFDG摄取值增高。远处转移:264%(14/53)的患者发生远处转移,主要位于肝和肺。转移癌 18FFDG摄取值增高。(3)PET/CT检查代谢参数值:53例食管原发灶:肿瘤SUVmax为163±62 (49~309),SUVavg为60±17(33~104),MTV为1814 cm3(774 cm3,2889 cm3),TLG为10537 g(4285 g,20562 g)。转移区域淋巴结:SUVmax为105±56(27~219)。远处转移癌:SUVmax为130±71(58~235)。(4)不同N、M分期的肿瘤代谢参数比较:N1~3期、N0期食管原发病灶的SUVmax分别为167±59、151±74,MTV分别为2092 cm3(1265 cm3,3573 cm3)、688 cm3(440 cm3,2153 cm3),TLG分别为13287 g(6549 g,22667 g)、3545 g(1753 g,12423 g)。N1~3期与N0期食管原发病灶的SUVmax比较,差异无统计学意义(t=-0785,P>005)。N1~3期食管原发病灶的MTV、TLG高于N0期,两者比较,差异均有统计学意义(Z=-2657,-2614,P<005)。M1期、M0期食管原发病灶的SUVmax分别为169±74、161±58,MTV分别为1614 cm3(833 cm3,2669 cm3)、2008 cm3(750 cm3,3134 cm3),TLG分别为9777 g(5115 g,15350 g)、10601 g(4016 g,21455 g)。M0期和M1期食管原发病灶的SUVmax、MTV、TLG间比较,差异均无统计学意义(t=0387,Z=-0282,-0383,P>005)。
    结论:食管癌 18FFDG PET/CT检查主要表现为食管局限性 18FFDG摄取值增高伴管壁增厚,常见于胸中段,且不同 N分期的食管原发病灶,MTV、TLG不同。PET/CT检查对显示食管原发病灶和转移癌具有一定临床价值。

     

    Abstract: 【Abstract】Objective:To summarize the imaging characteristics ship of Fluorine18fluorodeoxyglucose ( 18FFDG) PET/CT examination in esophageal carcinoma and the relation between metabolic parameters and stage.
    Methods:The clinical data of 53 patients with esophageal carcinoma who were admitted to the Changhai Hospital Affiliated to the Second Military Medical University between January 2012 and December 2014 were retrospectively analyzed. All the patients underwent 18FFDG PET/CT examination. The standardized uptake value 2.5 (SUV 2.5) was set as threshold value, and maximum SUV (SUVmax), average SUV (SUVavg), metabolic tumor volume (MTV) and maximum diameter of primary lesion were collected. The total lesion glycolysis (TLG) was calculated and SUVmax of lymph nodes in the metastasis area and distant metastasis carcinoma was measured. Measurement data with normal distribution were presented as ±s, and comparison between groups was evaluated with an independent sample the t test. Skew distribution data were described as M(Qn), and comparison between groups was analyzed using the MannWhitney test.
    Results:(1) Tumor location and volume: one tumor was located at the cervical portion of the esophagus, 16 at the upper thoracic portion, 18 at the midthoracic portion, 13 at the lower thoracic portion, 2 at the upper thoracic portion and midthoracic portion and 3 at the midthoracic portion and the lower thoracic portion. Tumor volume was 1.6 cm×1.2 cm×2.2 cm-6.5 cm×7.0 cm×7.2 cm and maximum diameter of tumor was (6.1±2.1)cm (range, 2.5-11.2 cm). (2) Performance of PET/CT examination: of 53 patients, 51 (96.2%) had 18FFDG uptake increased, thickening esophageal wall, unclear boundary between lesions and normal tissues and luminal stenosis of the lesion, and 2 (3.8%) had local nodular 18FFDG uptake increased without thickening esophageal wall. The infringement of the surrounding tissue organs was detected in 13 patients (24.5%), with unclear boundary between lesions with primary esophageal tumors and 18FFDG uptake increased. The regional lymph nodes metastasis was detected in 41 patients (77.4%), with 18FFDG uptake increased. The distal metastasis of 14 patients (26.4%) was located in the liver and lung, with 18FFDG uptake increased. (3) Metabolic parameters of PET/CT examination: SUVmax, SUVavg, MTV and TLG in the primary esophageal lesion of 53 patients were 16.3±6.2 (range, 4.9-30.9), 6.0±1.7 (range, 3.3- 10.4), 18.14 cm3 (7.74 cm3, 28.89 cm3) and 105.37 g (42.85 g, 205.62 g), respectively. SUVmax of regional lymph nodes metastasis and distant metastasis tumors were 10.5±5.6 (range, 2.7-21.9) and  13.0± 7.1 (range, 5.8-23.5). (4) Comparisons of metabolic parameters of tumors in different N, M stages: SUVmax, MTV and TLG were 16.7±5.9, 20.92 cm3 (12.65 cm3, 35.73 cm3) and 132.87 g (65.49 g, 226.67 g) in the N1-3 stage and 15.1±7.4, 6.88 cm3 (4.40 cm3, 21.53 cm3) and 35.45 g (17.53 g, 124.23 g) in the N0 stage, respectively, with no significant difference in the SUVmax between the N1-3 stage and N0 stage(t= -0.785, P>0.05). MTV and TLG of the primary esophageal lesion in the N1-3 stage were significantly higher than that in the N0 stage (Z=-2.657,-2.614, P<0.05). SUVmax, MTV and TLG of the primary esophageal lesion were 16.9±7.4, 16.14 cm3 (8.33 cm3, 26.69 cm3) and 97.77 g (51.15 g, 153.50 g) in the M1 stage, 16.1±5.8,20.08 cm3 (7.50 cm3, 31.34 cm3) and 106.01 g (40.16 g, 214.55 g) in the M0 stage, respectively, showing no significant difference between the M1 stage and M0 stage (t=0.387, Z=-0.282, -0.383, P>0.05).
    Conclusions:Imaging characteristics of 18FFDG PET/CT examination for esophageal carcinoma include the increase of 18FFDG uptake and local or extensive tube wall thickening, and N stage of primary esophageal lesion commonly located in the midthoracic portion is related to MTV and TLG. PET/CT examination shows a certain value to the primary and metastatic lesions of the esophagus.

     

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