Diagnostic ability of [18F]FDG PET/CT for distinguishing benign from malignant spleen lesions.

IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING European Radiology Pub Date : 2025-01-01 Epub Date: 2024-07-18 DOI:10.1007/s00330-024-10961-8
Dong Yun Lee, Yong-Il Kim, Jin-Sook Ryu
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Abstract

Objectives: [18F]Fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) is a non-invasive imaging modality used in the differential diagnosis of splenic lesions, although ideal parameters and thresholds remain unclear. The present study evaluated the ability of [18F]FDG PET/CT, including its visual and quantitative parameters, to differentiate between benign and malignant splenic lesions.

Methods: Patients who underwent [18F]FDG PET/CT following the detection of splenic lesions on contrast-enhanced CT were retrospectively analysed. Visual parameters assessed on [18F]FDG PET/CT included whole spleen uptake intensity, lesion multiplicity, and lesion uptake, and quantitative parameters included maximum standardised uptake value (SUVmax), lesion-to-background ratio (LBR), metabolic tumour volume (MTV), total lesion glycolysis (TLG), and lesion size. Parameters differentiating between benign and malignant lesions were evaluated by Pearson's chi-square test, Mann-Whitney U-test, and receiver operating characteristics (ROC) curve analysis.

Results: Splenic lesion uptake (p = 0.001) was the only visual parameter significantly distinguishing between benign and malignant lesions. ROC curve analysis demonstrated that SUVmax had the largest area under the ROC, 0.91 (p < 0.001), with an optimal cut-off > 5.3 having a sensitivity of 90.3% and a specificity of 80.6%. Subgroup analysis of malignant lesions showed that SUVmax (p = 0.013), LBR (p = 0.012), and TLG (p  = 0.034) were significantly higher in splenic lymphomas than in splenic metastases.

Conclusion: Of the [18F]FDG PET/CT parameters investigated, SUVmax had the highest accuracy in diagnosing malignant splenic lesions and was significantly higher in splenic lymphomas than in splenic metastases. Visual determination of [18F]FDG uptake by splenic lesions may be an easily evaluated parameter.

Clinical relevance statement: SUVmax and visual grade of [18F]FDG PET/CT help to differentiate spleen lesions. [18F]FDG PET/CT is useful for discriminating between benign and malignant spleen lesions.

Key points: Many splenic lesions are difficult to diagnose on anatomical imaging, with histopathologic analyses are required. SUVmax of PET/CT provided the diagnostic ability to differentiate between benign and malignant splenic lesions. More than normal spleen uptake can be a convenient parameter to diagnose malignant spleen lesions.

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18F]FDG PET/CT 鉴别脾脏良恶性病变的诊断能力。
目的:[18F]氟脱氧葡萄糖(FDG)正电子发射断层扫描/计算机断层扫描(PET/CT)是一种用于鉴别诊断脾脏病变的无创成像模式,但理想的参数和阈值仍不明确。本研究评估了[18F]FDG PET/CT 的能力,包括其视觉和定量参数,以区分良性和恶性脾脏病变:方法:对对比增强 CT 发现脾脏病变后接受[18F]FDG PET/CT 的患者进行回顾性分析。18F]FDG PET/CT 评估的视觉参数包括全脾摄取强度、病灶多度和病灶摄取,定量参数包括最大标准化摄取值 (SUVmax)、病灶与背景比值 (LBR)、代谢肿瘤体积 (MTV)、病灶糖酵解总量 (TLG) 和病灶大小。区分良性和恶性病变的参数通过皮尔逊卡方检验、曼-惠特尼U检验和接收器操作特性曲线分析进行评估:结果:脾脏病变摄取(p = 0.001)是唯一能显著区分良性和恶性病变的视觉参数。ROC 曲线分析表明,SUVmax 的 ROC 下面积最大,为 0.91(p 5.3),灵敏度为 90.3%,特异度为 80.6%。恶性病变亚组分析显示,脾淋巴瘤的 SUVmax(p = 0.013)、LBR(p = 0.012)和 TLG(p = 0.034)显著高于脾转移瘤:结论:在所研究的[18F]FDG PET/CT参数中,SUVmax诊断恶性脾病变的准确性最高,在脾淋巴瘤中明显高于脾转移瘤。目测脾脏病变对[18F]FDG的摄取可能是一个易于评估的参数:SUVmax和[18F]FDG PET/CT的肉眼分级有助于区分脾脏病变。临床意义:[18F]FDG PET/CT 有助于区分脾脏良性和恶性病变:要点:许多脾脏病变难以通过解剖成像诊断,需要进行组织病理学分析。PET/CT 的 SUVmax 具有区分良性和恶性脾脏病变的诊断能力。脾脏摄取超过正常值可作为诊断恶性脾脏病变的方便参数。
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来源期刊
European Radiology
European Radiology 医学-核医学
CiteScore
11.60
自引率
8.50%
发文量
874
审稿时长
2-4 weeks
期刊介绍: European Radiology (ER) continuously updates scientific knowledge in radiology by publication of strong original articles and state-of-the-art reviews written by leading radiologists. A well balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes ER an indispensable source for current information in this field. This is the Journal of the European Society of Radiology, and the official journal of a number of societies. From 2004-2008 supplements to European Radiology were published under its companion, European Radiology Supplements, ISSN 1613-3749.
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