Nagata Shuji, Nishimura Hiroshi, Uchida Masafumi, Hayabuchi Naofumi
Department of Radiology, Kurume University School of Medicine.
Nihon Igaku Hoshasen Gakkai Zasshi. 2005 Jan;65(1):30-6.
To evaluate the usefulness of diffusion-weighted MRI in distinguishing different components and in differentiating benign from malignant musculoskeletal tumors.
Fifty-seven patients with musculoskeletal tumors underwent MR at our institution from October 1999 to April 2002. We evaluated 57 tumors (9 bone tumors and 48 soft tissue tumors). All tumors were classified into 8 groups (myxomatous, fibrous, cystic, cartilaginous, fatty components, hematomas, other benign tumors, and other malignant tumors). MR examinations were performed with a 1.5-Tesla system. Diffusion-weighted single-shot EPI images were obtained in all patients. Apparent diffusion coefficients (ADCs) were calculated by using b factors of 0 and 1,000 sec/mm2.
ADC values of myxomatous, cystic, and cartilaginous components were significantly higher than those of other tumors. In cartilaginous tumors, malignant tumor ADC values (2.33 +/- 0.44) were higher than those of benign tumors (2.13 +/- 0.13). However, there was no significant difference between benign and malignant tumors. Except for high-intensity components on T1-weighted imaging and low or homogeneously very high intensity components on T2-weighted imaging, there was a significant difference in ADC between malignant (1.35 +/- 0.40) and benign (1.97 +/- 0.50) tumors.
Within the limited number of cases, there was a significant difference in ADC between malignant and benign tumors.
评估扩散加权磁共振成像(MRI)在区分不同成分以及鉴别肌肉骨骼系统良性和恶性肿瘤方面的效用。
1999年10月至2002年4月期间,57例患有肌肉骨骼系统肿瘤的患者在我院接受了磁共振成像检查。我们评估了57个肿瘤(9个骨肿瘤和48个软组织肿瘤)。所有肿瘤被分为8组(黏液样、纤维性、囊性、软骨性、脂肪成分、血肿、其他良性肿瘤和其他恶性肿瘤)。使用1.5特斯拉系统进行磁共振成像检查。所有患者均获得扩散加权单次激发回波平面成像(EPI)图像。通过使用b值为0和1000秒/平方毫米来计算表观扩散系数(ADC)。
黏液样、囊性和软骨性成分的ADC值显著高于其他肿瘤。在软骨性肿瘤中,恶性肿瘤的ADC值(2.33±0.44)高于良性肿瘤(2.13±0.13)。然而,良性和恶性肿瘤之间没有显著差异。除了T1加权成像上的高强度成分以及T2加权成像上的低强度或均匀的非常高强度成分外,恶性肿瘤(1.35±0.40)和良性肿瘤(1.97±0.50)之间的ADC存在显著差异。
在病例数量有限的情况下,恶性和良性肿瘤之间的ADC存在显著差异。