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首页> 外文期刊>European radiology >Alveolar soft-part sarcoma: can MRI help discriminating from other soft-tissue tumors? A study of the French sarcoma group
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Alveolar soft-part sarcoma: can MRI help discriminating from other soft-tissue tumors? A study of the French sarcoma group

机译:肺泡软部分肉瘤:MRI有助于区分其他软组织肿瘤吗? 法国肉瘤集团的研究

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摘要

ObjectivesTo investigate the imaging features of alveolar soft-part sarcomas (ASPS) on pre-treatment MRI in order to identify relevant criteria to distinguish ASPS from other soft-tissue tumors.MethodsA series of 25 patients (mean age, 18.5years old) with histologically proven ASPS from five French comprehensive cancer centers was compared to a control cohort of 292 patients with various histologically proven benign and malignant soft-tissue tumors representative of the 10-year long activity of one center. All had a baseline MRI with contrast-agent administration. Two radiologists independently reviewed the MRIs. Features assessing location, size, signal, architecture, periphery, and vascularization were reported. Their association with the histological diagnosis of ASPS was evaluated with chi-square or Fisher's test. Their prevalence, sensitivity, specificity, odds ratio, and reproducibility were calculated.ResultsEight MRI features were significantly associated with ASPS: deep location (p<0.001), high signal intensities on T1-weighted imaging (p<0.001), central area of necrosis (p=0.001), absence of fibrotic component (p=0.003), infiltrative growth pattern (p=0.003), absence of tail sign (p=0.001), presence of intra- and peritumoral flow-voids (p<0.001), and number of flow-voids 5 (p<0.001). Twenty out of the 25 (80%) ASPS showed at least 7 of these 8 features compared to only four out of 292 (1.4%) tumors of the control cohort (1 benign vascular tumor, 1 solitary fibrous tumor, 2 high-grade soft-tissue sarcomas). The five ASPS with less than 7 out of 8 features measured less than 40mm.ConclusionThe striking histological uniformity of ASPS translates into imaging. However, ASPS may be misdiagnosed as benign tumors or pseudo-tumors, notably intramuscular benign vascular tumors or vascular malformations.Key Points center dot ASPS are rare aggressive mesenchymal tumors displaying recurrent MRI features highly reminiscent of the diagnosis.center dot Deep-seated tumors presenting with mainly high signal intensity on T1-weighted imaging, an absence of fibrotic component, ill-defined margins without aponeurotic extension, and more than five central and peripheral flow-voids are very likely to be ASPS.center dot ASPS may be misdiagnosed as intramuscular benign vascular tumor or vascular malformation, which occur in the same age group.
机译:Objectivesto在预处理MRI上调查肺泡软部分SARCOMAS(ASP)的成像特征,以确定相关标准,以区分ASPS与其他软组织肿瘤的影响。一系列25名患者(平均年龄,18.5岁),组织学上从五个法国综合癌症中心的验证亚马斯与292名患者的控制队列相比,各种组织学证明良性和恶性软组织肿瘤的患者,代表了一个中心的10年期间的长期活动。所有人都有一个具有鲜明剂管理的基线MRI。两个放射科医生独立审查了MRIS。报告了评估位置,大小,信号,架构,周边和血管化的特点。与Chi-Square或Fisher的测试评估了它们与ASP的组织学诊断的关联。计算普遍性,敏感性,特异性,差距和再现性。培养MRI特征与ASPS显着相关:深度位置(P <0.001),T1加权成像的高信号强度(P <0.001),中央区域的坏死(p = 0.001),没有纤维化组分(p = 0.003),渗透生长模式(p = 0.003),尾标志(p = 0.001),存在内和腹膜流动空隙(p <0.001),和流动空隙的数量5(p <0.001)。 25(80%)ASP中的25个(80%)显示这些8个特征中的至少7个,只有4个422(1.4%)肿瘤的4个(1.4%)肿瘤(1个良性血管肿瘤,1个孤立纤维肿瘤,2个高档柔软-tissue sarcomas)。 8个特征中的五个截止物,测量小于40mm。结论ASP的组织学均匀性转化为成像。然而,ASPS可能被误诊为良性肿瘤或伪肿瘤,特别是肌肉内良性血管肿瘤或血管畸形。时,中心点ASP是罕见的腐蚀性间充质肿瘤,显示复发性MRI特征高度让人诊断。CONTER DOT深层肿瘤呈现以T1加权成像的主要高信号强度,不存在纤维化组分,没有腱膜延伸的不含脊柱的边缘,并且超过五个中央和周边流动空隙非常可能是ASPS.Center点ASP可能被误诊为肌肉内良性血管肿瘤或血管畸形,在同一年龄组中发生。

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