Bhargava R, Parham D M, Lasater O E, Chari R S, Chen G, Fletcher B D
Department of Diagnostic Imaging, St. Jude Children's Research Hospital, 332 N. Lauderdale St., Memphis, TN 38101, USA.
Pediatr Radiol. 1997 Feb;27(2):124-9. doi: 10.1007/s002470050082.
T2-weighted MR imaging of soft tissue tumors of neural origin may show round lesions with a central hypointensity and a hyperintense rim resembling a target. We define the "target sign" as a mass consisting of a solitary target, or a multicompartmental mass in which the largest component consists of multiple targets.
The objective of this study was to determine whether the target sign can differentiate benign neurofibromas and their malignant counterparts, malignant peripheral nerve sheath tumors. Materials and methods. Preoperative T2-weighted MR images of 23 neurofibromas or malignant peripheral nerve sheath tumors were retrospectively reviewed in 16 patients, aged 3 weeks to 20 years (median 15 years), without knowledge of the pathologic diagnosis. The presence or absence of a target sign was noted.
The target sign was seen in all 12 neurofibromas and 1 of the 11 malignant peripheral nerve sheath tumors. Statistical analysis showed good differentiation of benign and malignant tumors using this sign (chi = 0.91).
The target sign on T2-weighted MR imaging is helpful in differentiating neurofibromas from malignant peripheral nerve sheath tumors.
神经源性软组织肿瘤的T2加权磁共振成像可能显示圆形病灶,中央低信号,边缘高信号,类似靶征。我们将“靶征”定义为单个靶征组成的肿块,或多房性肿块,其中最大的成分由多个靶征组成。
本研究的目的是确定靶征是否能够区分良性神经纤维瘤及其恶性对应物,即恶性外周神经鞘瘤。材料与方法。回顾性分析16例年龄3周~20岁(中位年龄15岁)患者的23例神经纤维瘤或恶性外周神经鞘瘤的术前T2加权磁共振图像,且不知病理诊断结果。记录有无靶征。
12例神经纤维瘤均可见靶征,11例恶性外周神经鞘瘤中有1例可见靶征。统计学分析显示,利用该征象可很好地区分良性和恶性肿瘤(χ=0.91)。
T2加权磁共振成像上的靶征有助于区分神经纤维瘤和恶性外周神经鞘瘤。