The role of positron emission tomography using carbon-11 and fluorine-18 choline in tumors other than prostate cancer: a systematic review

To systematically review published data on the role of positron emission tomography (PET) or PET/computed tomography (PET/CT) using either Carbon-11 ((11)C) or Fluorine-18 ((18)F) choline tracer in tumors other than prostatic cancer. A comprehensive literature search of studies published in PubMed/MEDLINE and Embase databases through January 2012 and regarding (11)C-choline or (18)F-choline PET or PET/CT in patients with tumors other than prostatic cancer was carried out. Fifty-two studies comprising 1800 patients were included and discussed. Brain tumors were evaluated in 15 articles, head and neck tumors in 6, thoracic tumors (including lung and mediastinal neoplasms) in 14, liver tumors (including hepatocellular carcinoma) in 5, gynecologic malignancies (including breast tumors) in 5, bladder and upper urinary tract tumors in 5, and musculoskeletal tumors in 7. Radiolabeled choline PET or PET/CT is useful to differentiate high-grade from low-grade gliomas and malignant from benign brain lesions, to early detect brain tumor recurrences and to guide the stereotactic biopsy sampling. The diagnostic accuracy of radiolabeled choline PET is superior compared to Fluorine-18 fluorodeoxyglucose ((18)F-FDG) PET in this setting. Radiolabeled choline PET or PET/CT seems to be accurate in differential diagnosis between malignant and benign thoracic lesions and in staging lung tumors; nevertheless, a superiority of radiolabeled choline compared to (18)F-FDG has not been demonstrated in this setting, except for the detection of brain metastases. Few but significant studies on radiolabeled choline PET and PET/CT in patients with hepatocellular carcinoma (HCC) and musculoskeletal tumors are reported in the literature. The combination of radiolabeled choline and (18)F-FDG PET increases the detection rate of HCC. The diagnostic accuracy of radiolabeled choline PET or PET/CT seems to be superior compared to (18)F-FDG PET or PET/CT and conventional imaging methods in patients with bone and soft tissue tumors. Limited experience exists about the role of radiolabeled choline PET and PET/CT in patients with head and neck tumors, bladder cancer and gynecologic malignancies including breast cancer.     

A seldom case of primary urethral malignant melanoma and breast cancer detected by (18)F-FDG PET/CT

In the 1(st )issue of HJNM for 2012 we read with interest a case where 3 different cancers were detected. Synchronous second malignancy can be incidentally detected in routine fluorine-18-fluoro-deoxy-glucose positron emission tomography/computed tomography ( (18)F-FDG PET/CT) imaging in approximately 1% of cancer patients with lungs being the most frequent site. We report the (18)F-FDG PET/CT scan for staging of the primary malignant melanoma of the urethra and for the detection of another malignancy in the breast in the same patient, since primary malignant melanoma of urethra is very seldom. A 65 years old post-menopausal woman presented with increased frequency of micturition, dysuria and a gradually enlarging mass protruding from the external urethral meatus. Fine needle aspiration cytology (FNAC) performed from the mass revealed malignant melanoma. On cystourethrescopy examination, a 4x4 cm blackish mass was noted at the external urethral meatus with a satellite nodule in the bladder trigone. Contrast enhanced CT (CeCT) of the pelvis showed soft tissue thickening along the urethra infiltrating urinary bladder neck and vagina. Analysis of (18)F-FDG PET/CeCT was performed to assess the extent of the disease. Intensely (18)F-FDG avid soft tissue mass (SUV(max): 20.1) was noticed along the entire length of the urethra with hypermetabolic right inguinal and left external iliac lymph nodes. In addition to (18)F-FDG uptake in the bladder wall and the vaginal wall, intense (18)F-FDG uptake was also seen in two soft tissue nodules in the right breast and in the axillary lymph nodes suggestive of a second primary in the breast. Cytological diagnosis of intraductal breast carcinoma was made after FNAC from the breast nodule. Urethral melanoma was treated with anterior exenteration and ileal conduit. Histopathology confirmed the diagnosis of primary malignant melanoma of urethra infiltrating the urinary bladder and anterior vaginal wall. Postoperative histopathology from the right inguinal and left external iliac lymph nodes revealed metastatic disease. The diagnostic contribution of PET/CT was crucial. Melanotic melanoma cells have a distinctive MRI signal, which may be helpful in diagnosis. In this case whole body MRI could have been of equal value for accurate staging of urethral melanoma, but whole body MRI is a cumbersome procedure and often is not practical. Primary urethral carcinoma is very rare and an annual ageadjusted incidence rate of 4.3 per 106 in males and 1.5 per 106 in females has been reported in USA. Primary malignant melanoma of the urethra is rare, representing less than 1% of all melanomas and 4% of urethral cancers. Furthermore, the incidence of two primary cancers is rare and is reported to be between 0.3% and 4.3%. Primary malignant melanoma of the urethra has a worse prognosis than its cutaneous counterpart, partly due to delayed diagnosis. At the time of diagnosis, urethral melanoma is usually deeply invasive and locally extended to the vagina or vulva or the corpora cavernosa. Inguinal lymph node metastases are present at diagnosis in half of the cases and distant metastases in one third of them. Positron emission tomography demonstrates specificity and accuracy of 94.7% and 73% respectively in detecting lymph nodal metastases. Sensitivity, specificity and accuracy of (18)F-FDG PET/CT in detecting metastases in high risk patients were 85%, 96%, 91% while for (18)F-FDG PET/CT with dedicated CT interpretation were 98%, % and 96%, respectively. Recently, the role of (18)F-FDG PET/CT in treatment response evaluation of melanoma patients has also been demonstrated. Incidental (18)F-FDG uptake in the breasts is rare, and the lesion may be malignant in up to 57% of the cases. To our knowledge no published literature is available on synchronous breast carcinoma and urethral melanoma. The reason why some patients are more prone to develop multiple cancers remains obscure. One possibility may be of a genetic predisposition linking the two cancers. Research suggests that mutations in CDKN2A, a gene that indicates high risk of developing melanoma, also puts carriers at an up to 3.8 times greater risk of breast cancer. Similarly, mutations in the gene of breast cancer susceptibility, BRCA2, increase carriers' risk of melanoma by as much as 2.58 times. In conclusion, we describe a case of two primary carcinomas: a unique urethral malignant melanoma and a breast carcinoma, detected and staged by (18)F-FDG PET/CT.     

18F-FDG PET/CT delayed images after diuretic for restaging invasive bladder cancer.

PET with (18)F-FDG has been considered of limited value for detection of bladder cancer because of the urinary excretion of the tracer. The purpose of this study was to investigate the role of PET/CT in the detection and restaging of bladder cancer using furosemide and oral hydration to remove the excreted (18)F-FDG from the bladder. METHODS: Seventeen patients with bladder cancer (11 without cystectomy, 6 with total cystectomy and urinary diversion) underwent (18)F-FDG PET/CT from head to the upper thighs 60 min after the intravenous injection of 370 MBq of (18)F-FDG. Additional pelvic images were acquired 1 h after the intravenous injection of furosemide and oral hydration. PET/CT findings were confirmed by MRI, cystoscopy, or biopsy. RESULTS: PET/CT was able to detect bladder lesions in 6 of 11 patients who had not undergone cystectomy. These images changed the PET/CT final reading in 7 patients: Recurrent bladder lesions were detected in 6 patients, pelvic lymph node metastases in 2 patients, and prostate metastasis in 1. This technique overcame the difficulties posed by the urinary excretion of (18)F-FDG. Hypermetabolic lesions could be easily detected by PET and precisely localized in the bladder wall, pelvic lymph nodes, or prostate by CT. Seven of 17 patients (41%) were upstaged only after delayed pelvic images. CONCLUSION: Detection of locally recurrent or residual bladder tumors can be dramatically improved using (18)F-FDG PET/CT with delayed images after a diuretic and oral hydration.     

18F-氟代脱氧葡萄糖PET在肾恶性肿瘤中的应用

18F-氟代脱氧葡萄糖(18F-FDG)PET在肾恶性肿瘤中主要应用于原发肿瘤定性诊断和分期、肿瘤局部复发及远处转移病灶诊断等。PET检查对选择治疗方案的影响主要由于发现远处转移病灶和对病灶定性。并优于CT等常规检查。但18F-FDG PET对诊断原发性肾细胞癌敏感性低于CT,可能与肿瘤分级或某些特性有关。     

18F-FDG PET and CT/MRI in oral cavity squamous cell carcinoma: a prospective study of 124 patients with histologic correlation.

Accurate evaluation of primary tumors and cervical lymph node status of squamous cell carcinoma (SCC) of the oral cavity is important to treatment planning and prognosis prediction. In this prospective study, we evaluated the use of 18F-FDG PET, CT/MRI, and their visual correlation for the identification of primary tumors and cervical nodal metastases of SCC of the oral cavity with histologic correlation. METHODS: One hundred twenty-four patients with pathologically proven diagnoses of oral cavity SCC underwent 18F-FDG PET and CT/MRI within 2 wk before surgery. We interpreted 18F-FDG PET, CT/MRI, and visually correlated 18F-FDG PET and CT/MRI separately to assess the primary tumors and their regional lymph node status. We recorded lymph node metastases according to the neck level system of imaging-based nodal classification. Histopathologic analysis was used as the gold standard for assessment of the primary tumors and lymph node involvement. We analyzed differences in sensitivity and specificity among the imaging modalities using the McNemar test. The receiver-operating-characteristic (ROC) curve and calculation of the area under the curve were used to evaluate their discriminative power. RESULTS: The accuracy of 18F-FDG PET, CT/MRI, and their visual correlation for the identification of primary tumors was 98.4%, 87.1%, and 99.2%, respectively. The sensitivity of 18F-FDG PET for the identification of nodal metastases on a level-by-level basis was 22.1% higher than that of CT/MRI (74.7% vs. 52.6%, P < 0.001), whereas the specificity of 18F-FDG PET was 1.5% lower than that of CT/MRI (93.0% vs. 94.5%, P = 0.345). The sensitivity and specificity of the visual correlation of 18F-FDG PET and CT/MRI were 3.2% and 1.5% higher than those of 18F-FDG PET alone (77.9% vs. 74.7%, P = 0.25; 94.5% vs. 93.0%, P = 0.18, respectively). The area under the curve obtained from the ROC curve showed that 18F-FDG PET was significantly superior to CT/MRI for total nodal detection (0.896 vs. 0.801, P = 0.002), whereas the visual correlation of 18F-FDG PET and CT/MRI was modestly superior to 18F-FDG PET alone (0.913 vs. 0.896, P = 0.28). CONCLUSION: 18F-FDG PET is superior to CT/MRI in the detection of cervical status of oral cavity SCC. The sensitivity of 18F-FDG PET for the detection of cervical nodal metastasis on a level-by-level basis was significantly higher than that of CT/MRI, whereas their specificities appeared to be similar. Visual correlation of 18F-FDG PET and CT/MRI showed a trend of increased diagnostic accuracy over 18F-FDG PET alone but without a statistically significant difference, and its sensitivity was still not high enough to replace pathologic lymph node staging based on neck dissection.     

18F-FDG PET/CT在胃癌中的临床应用进展

胃癌是全球范围内最常见的恶性肿瘤之一。18F-氟脱氧葡萄糖（FDG）PET/CT在胃癌中的应用既有优点又有局限性。胃癌原发灶对18F-FDG的摄取与癌症分期、组织学分型和肿瘤大小密切相关。早期胃癌18F-FDG摄取阳性预示着内镜黏膜下剥离术的不可治愈性。进展期胃癌的最大标准化摄取值（SUV_max）在肠型与印戒细胞癌（SRC）或弥漫型胃癌间的差异显著,SRC的SUV_max与患者的总生存时间和无病生存时间呈负相关。18F-FDG PET/CT对区域淋巴结转移的诊断灵敏度较低,但其特异度很高,区域淋巴结对18F-FDG摄取呈阳性是预后不良的指征。18F-FDG PET/CT可检出隐匿的远处转移（7.2%~10.0%）,其中大部分（4.7%~8.8%）使用腹腔镜也不能检出。常规性应用18F-FDG PET/CT并联合腹腔镜检查对明确胃癌分期的意义重大。因此,笔者就18F-FDG PET/CT在胃癌中的临床应用进展进行综述。     

18F-FDG PET/CT诊断多发癌的价值

目的 探讨18F-FDG PET/CT在多发癌诊断中的价值。 方法 回顾性分析5822例疑似肿瘤患者,均行18F-FDG PET/CT全身检查,经过活检或手术证实为多发癌患者32例。以病理结果作为金标准,以PET平均标准化摄取值（SUV_mean）≥2.5且CT上有形态学改变者作为PET/CT判断恶性肿瘤的标准,计算PET/CT诊断多发癌的灵敏度和准确率。 结果 本组患者中多发癌的发生率为0.55%,其中,双发癌30例、三发癌2例,共66个原发灶。32例多发癌的66个原发灶的SUV_mean的平均值为6.68±3.61。PET/CT诊断多发癌原发灶真阳性为58个,假阴性为8个。PET/CT诊断多发癌的灵敏度为87.9%,准确率为87.9%。 结论 18F-FDG PET/CT全身检查诊断多发癌具有较大价值。     

18F-FDG PET显像在胰腺恶性病变鉴别诊断及转移灶探查中的应用价值

目的研究18F-FDGPET显像在胰腺恶性肿瘤诊断与鉴别诊断中的应用价值。方法 40例临床疑为胰腺恶性病变的患者均行18F-FDGPET显像,对显像结果进行目测法及SUV值半定量分析,并结合CT,MRI等影像学检查进行综合诊断,最后诊断根据手术病理或经4个月以上随访证实。结果如果以SUV为2.5作为鉴别诊断胰腺病灶良恶性的阈值,24例证实为胰腺癌患者中18F-FDGPET显像正确诊断22例,16例胰腺良性病变患者18F-FDGPET检出13例,其灵敏度、特异度及准确性分别为91.7%（22/24）,81.3%（13/16）及87.5%（35/40）;而结合CT,MRI等其他检查结果进行综合诊断,其诊断灵敏度、特异度及准确性分别为91.7%（22/24）、87.5%（14/16）及90%（36/40）。恶性病变的SUV平均值为4.6±2.6,良性病变的SUV平均值为2.3±1.5,良恶性病变间SUV平均值差异有统计学意义（P〈0.01）。在转移灶的检出中,18F-FDGPET显像发现了全部38处转移灶,并发现6处CT,MRI未能发现的远处转移病灶,排除了1例CT认为是胰周转移性淋巴结肿大的病例。结论 18F-FDGPET对鉴别诊断胰腺良恶性肿瘤的灵敏度、特异性较高,尤其在远处转移灶的探查中有较高应用价值。     

Pictorial review of <Superscript>18</Superscript>F-FDG PET/CT findings in musculoskeletal lesions

We herein reviewed ¹⁸F-fluoro-2-deoxyglucose (¹⁸F-FDG) positron emission tomography (PET)/computed tomography (CT) findings in a number of musculoskeletal lesions including malignant tumors, benign tumors, and tumor-like lesions with correlations to other radiographic imaging modalities, and described the diversity of the ¹⁸F-FDG PET/CT findings of this entity. Malignant primary musculoskeletal tumors are typically ¹⁸F-FDG avid, whereas low-grade malignant tumors show mild uptake. Benign musculoskeletal tumors generally show a faint uptake of ¹⁸F-FDG, and tumor-like conditions also display various uptake patterns of ¹⁸F-FDG. Although musculoskeletal tumors show various uptakes of ¹⁸F-FDG on PET/CT, its addition to morphological imaging modalities such as CT and MRI is useful for the characterization and differentiation of musculoskeletal lesions.     

多发性骨血管瘤 18F-FDG PET/CT显像一例

笔者报道了1例多发性骨血管瘤（IH） 18F-氟脱氧葡萄糖（FDG）PET/CT显像的病例,从临床症状、实验室检查和影像学表现等方面进行鉴别诊断。不同部位的IH的影像学表现各异,而 18F-FDG PET/CT能为临床鉴别肿瘤的良恶性提供参考。由于发生于扁平骨的IH非常少见,且其影像学表现缺乏特异性...     

Lymph node staging of gastric cancer using (18)F-FDG PET: a comparison study with CT.

This study was performed to compare (18)F-FDG PET with CT for the evaluation of primary tumors and lymph node metastases in gastric cancer. METHODS: Eighty-one patients (28 women and 53 men; mean age, 56.6 y; age range; 32-82 y) who had undergone radical (n = 74) or palliative (n = 7) gastrectomy and lymph node dissection for the management of gastric cancer were included. Preoperative (18)F-FDG PET and CT were reviewed retrospectively for primary tumors of the stomach and lymph node metastases. Any increased (18)F-FDG uptake exceeding that of the adjacent normal gastric wall was considered positive for the primary tumor. Lymph nodes were classified into 3 groups based on their anatomic sites. Because perigastric lymph nodes (N1) were often not clearly differentiated from primary tumors, N1 lymph node metastases were determined when possible. Lymph nodes were considered positive or negative on the basis of the group as a whole. Final conclusions for primary tumors and lymph node metastases were based on histopathologic specimens in all patients. RESULTS: There were 17 patients with early gastric cancer (EGC) and 64 patients with advanced gastric cancer (AGC). For primary tumors, both PET and CT showed a sensitivity of 47% (8/17) for EGC and 98% (63/64) for AGC. The sensitivity of CT for N1 disease was significantly higher than that of PET. (18)F-FDG PET had a sensitivity, specificity, and accuracy of 34% (11/32), 96% (47/49), and 72% (58/81), respectively, for N2 metastases, whereas the corresponding CT values were 44% (14/32), 86% (42/49), and 69% (56/81). For N3 metastases, PET and CT had the same sensitivity, specificity, and accuracy: 50% (3/6), 99% (74/75), and 95% (77/81), respectively. Overall, the sensitivity, specificity, and accuracy of (18)F-FDG PET were not significantly different from those of CT for primary tumors or for N2 and N3 metastases. CONCLUSION: (18)F-FDG PET is as accurate as CT for the detection of primary tumors of either EGC or AGC. The low sensitivities of PET and CT were insufficient to allow decision making on the extent of lymphadenectomy. In contrast, the high specificity of PET for N disease appeared valuable, and the presence of N disease on PET may have a clinically significant impact on the choice of initial therapy.     

18F-FDG PET/CT与增强CT在成人原发前纵隔恶性肿瘤中的诊断价值

目的 探讨18F-氟脱氧葡萄糖（FDG） PET/CT与增强CT在成人原发前纵隔恶性肿瘤中的诊断价值,以提高对该部位病变的诊断水平。 方法 回顾性分析2016年6月至2019年5月在湖北文理学院附属医院（襄阳市中心医院）经病理证实的成人原发前纵隔肿瘤患者80例（恶性肿瘤35例、良性肿瘤45例）,其中,男性46例、女性34例,年龄20~80（45.5±10.2）岁。所有患者均行全身18F-FDG PET/CT及胸部CT平扫+增强扫描,2种检查的间隔时间在2周内。分别计算并采用χ2检验比较18F-FDG PET/CT与增强CT扫描的诊断灵敏度、特异度和准确率,采用χ2检验比较2种检查方法对不同类型恶性肿瘤的诊断效能。 结果 35例恶性肿瘤中胸腺癌15例,淋巴瘤10例,恶性生殖细胞瘤7例,神经内分泌癌、恶性黑色素瘤及滑膜肉瘤各1例。18F-FDG PET/CT诊断成人原发前纵隔恶性肿瘤的灵敏度[97.1%（34/35）]、特异度[93.3%（42/45）]及准确率[95.0%（76/80）]均高于增强CT[71.4%（25/35）、77.8%（35/45）、75.0%（60/80）],且差异有统计学意义（χ2=8.612、4.357、12.471,均P<0.05）;18F-FDG PET/CT对胸腺癌、淋巴瘤及恶性生殖细胞瘤诊断的准确率[93.3%（14/15）、100.0%（10/10）、85.7%（6/7）]均高于增强CT[60.0%（9/15）、50.0%（5/10）、28.6%（2/7）],且差异有统计学意义（χ2=4.503、6.333、4.333,均P<0.05）。 结论 18F-FDG PET/CT对成人原发前纵隔恶性肿瘤具有重要的诊断价值,其诊断效能优于增强CT,可作为该病主要的检查方法。     

18F-FDG PET/CT在黑色素瘤中的应用价值

目的 探讨18F-脱氧葡萄糖(FDG)PET/CT显像在黑色素瘤诊断、临床分期及监测治疗后肿瘤复发与转移灶中的应用价值.方法 黑色素瘤患者61例,均进行18F-FDG PET/CT全身显像.所有PET、CT及PET/CT融合图像均通过融合软件进行帧对帧对比分析.肿瘤病灶根据病理学检查、多种影像学检查及临床随访结果诊断.结果 18F-FDG PET/CT显像对黑色素瘤病灶检出的灵敏度、特异性和准确性分别为90.9%(40/44)、88.2%(15/17)和90.2%(55/61).其中12例治疗前患者中,18F-FDG PET/CT显像诊断的灵敏度为83.3%(10/12).在黑色素瘤病灶局部切除、尚未进行其他治疗的9例患者中,5例残余病灶18F-FDG PET/CT显像检出3例;4例远处转移灶患者全被检出,提高了临床分期,改变了治疗方案.首先发现转移性黑色素瘤病灶并且手术切除后,寻找原发灶的7例患者中,18F-FDG PET/CT检出原发灶2例,4例其他转移灶全被检出.黑色素瘤患者根治术后监测肿瘤复发或转移患者33例,18F-FDG PET/CT显像灵敏度、特异性和准确性分别为100.0%(19/19)、85.7%(12/14)和93.9%(31/33).与同期临床其他影像学检查比较,18F-FDG PET/CT显像发现更多,33例患者中,16例(48.5%)病灶提高临床分期;7例(21.2%)排除可疑病灶,降低临床分期;10例(30.3%)检出病灶与临床一致.结论 18F-FDG PET/CT显像对于黑色素瘤的诊断,残余病灶、复发病灶及转移灶的检出,临床分期的明确具有重要价值.     

18F-FDG PET/CT在原发灶不明的脑转移瘤中的诊断价值

目的 探讨18F-FDG PET/CT在查找原发灶不明的脑转移瘤中的价值。 方法 回顾性分析17例原发灶不明的脑转移瘤患者的全身18F-FDG PET/CT检查资料。 结果 17例患者均经活检确诊原发灶,准确率100%。原发性肺癌13例,占76%,其中有2例在第二次行PET/CT检查时才检出原发灶;原发性肝癌2例,占12%;原发性贲门癌1例,占6%;原发性升结肠癌1例,占6%。在检查到原发灶的基础上,18F-FDG PET/CT亦发现10例合并转移者,其中合并肺转移者2例、合并淋巴结转移者3例、合并骨转移者2例及合并其他部位转移者3例,共发现病灶61处;2例肝癌患者单发脑转移灶中均有脑卒中。 结论 18F-FDG PET/CT在查找原发灶不明的脑转移瘤原发灶中有重要价值,并为临床分期及治疗提供有利帮助。     

11C-胆碱和18F-FDG PET/CT显像在脑胶质瘤诊断中的应用

目的 探讨11C-胆碱和18F-FDG PET/CT在脑胶质瘤显像中的意义,以提高PET/CT对脑胶质瘤病变的诊断价值。 方法 分别对21例颅脑占位疑似脑胶质瘤患者行11C-胆碱及18F-FDG PET/CT颅脑显像,分析11C-胆碱和18F-FDG最大标准化摄取值（SUV_max）与患者年龄、病理类型之间的关系。 结果 21例患者的18F-FDG和11C-胆碱SUV_max与患者年龄无显著相关性,18F-FDG SUV_max与病变的良、恶性也无显著相关性,而11C-胆碱SUV_max与病变良、恶性存在一定相关性。 结论 11C-胆碱PET/CT在诊断和鉴别颅内胶质瘤病变中具有重要的价值和意义。     

Spectrum of malignant renal and urinary bladder tumors on 18F-FDG PET/CT: a pictorial essay

A wide variety of malignant renal and urinary bladder diseases can be detected on ¹⁸F-FDG PET/CT. Although the PET/CT findings are often nonspecific, the aim of this atlas was to demonstrate that the spectrum of renal and urinary bladder malignancy that can be evaluated with PET/CT is much broader than current medical literature would suggest. PET/CT readers and oncologists should be aware of the variety of urological tumor types that can be detected on PET/CT and some of the patterns of ¹⁸F-FDG uptake that can be observed in these cases.     

胃腺癌乳腺转移18F-FDG PET/CT显像一例

笔者报道了1例胃腺癌乳腺转移18F-氟脱氧葡萄糖（FDG）PET/CT显像的病例,从临床表现、18F-FDG PET/CT影像学表现、病理诊断及鉴别诊断等方面分析了该病的特点。胃腺癌乳腺转移在临床上罕见,临床表现缺乏特异性,易漏诊及误诊,确诊需经组织病理学检查。18F-FDG PET/CT检查可以早期筛查全身病灶,提高诊断的准确率。     

18F-FDG PET/CT在前列腺癌中的应用进展

前列腺癌是临床常见的恶性肿瘤之一,在我国的发病率呈逐年上升趋势。18F-FDG是一种广谱的肿瘤非特异性显像剂,在多数肿瘤的临床应用中都具有重要价值。但临床实践表明,18F-FDG PET/CT显像在前列腺癌早期诊断中的价值是有限的。随着认识的深入,人们发现其在前列腺癌临床分期、疗效评价、预后评估等方面仍具有重要价值。笔者将对18F-FDG PET/CT在前列腺癌中的应用进展予以综述。     

Breast cancer staging in a single session: whole-body PET/CT mammography

Our objective was to compare the diagnostic accuracy of an all-in-one protocol of whole-body 18F-FDG PET/CT and integrated 18F-FDG PET/CT mammography with the diagnostic accuracy of a multimodality algorithm for initial breast cancer staging. METHODS: Forty women (mean age, 58.3 y; range, 30.8-78.4 y; SD, 12 y) with suspected breast cancer were included. For the primary tumor, we compared 18F-FDG PET/CT mammography versus MRI mammography; for axillary lymph node status, 18F-FDG PET/CT versus clinical investigation and ultrasound; and for distant metastases, 18F-FDG PET/CT versus a multimodality staging algorithm. Histopathology and clinical follow-up served as the standard of reference. The Fisher exact test evaluated the significance of differences (P < 0.05). Alterations in patient management caused by 18F-FDG PET/CT were documented. RESULTS: No significant differences were found in the detection rate of breast cancer lesions (18F-FDG PET/CT, 95%; MRI, 100%; P = 1). 18F-FDG PET/CT correctly classified lesion focality significantly more often than did MRI (18F-FDG PET/CT, 79%; MRI, 73%; P < 0.001). MRI correctly defined the T stage significantly more often than did 18F-FDG PET/CT (MRI, 77%; 18F-FDG PET/CT, 54%; P = 0.001). 18F-FDG PET/CT detected axillary lymph node metastases in 80% of cases; clinical investigation/ultrasound, in 70%. This difference was not statistically significant (P = 0.067). Distant metastases were detected with 18F-FDG PET/CT in 100% of cases, and the multimodality algorithm identified distant metastases in 70%. This difference was not statistically significant (P = 1). Three patients had extraaxillary lymph node metastases that were detected only by PET/CT (cervical, retroperitoneal, mediastinal/internal mammary group). 18F-FDG PET/CT changed patient management in 12.5% of cases. CONCLUSION: Our data suggest that a whole-body 18F-FDG PET/CT mammography protocol may be used for staging breast cancer in a single session. This initial assessment of the 18F-FDG PET/CT protocol indicates similar accuracy to MRI for the detection of breast cancer lesions. Although MRI seems to be more accurate when assessing the T stage of the tumor, 18F-FDG PET/CT seems able to more accurately define lesion focality. Although 18F-FDG PET/CT mammography was able to detect axillary lymph node metastases with a high sensitivity, this method cannot soon be expected to replace the combination of clinical examination, ultrasound, and sentinel lymph node biopsy for axillary assessment.     

18 F-FDG PET/CT显像探测原发肿瘤病灶的临床价值

目的探讨^18F-脱氧葡萄糖(FDG)PET/CT显像寻找原发肿瘤病灶的价值。方法对临床诊断转移瘤患者31例行唧CT显像，将其诊断结果与手术、活组织检查及临床随访结果对照。结果29例患者唧CT显像准确显示其原发灶，分别为结、直肠癌7例，肺癌13例，甲状腺癌3例，子宫恶性肿瘤4例，胰腺癌和鼻咽癌各1例。1例PET/CT检查未能确定其原发灶。另1例临床诊断为肾上腺转移瘤的患者，PET/CT显像为良性肿瘤，经CT动态增强检查及实验室检查证实。结论PET／CT显像对寻找转移瘤原发灶有重要价值。