Dysembryoplastic neuroepithelial tumors: magnetic resonance imaging and magnetic resonance spectroscopy evaluation

被引:8
作者
Yu Ai-hong [1 ]
Chen Li [2 ]
Li Yong-jie [1 ]
Zhang Guo-jun [1 ]
Li Kun-cheng [3 ]
Wang Yu-ping [4 ]
机构
[1] Capital Med Univ, Xuanwu Hosp, Beijing Inst Funct Neurosurg, Beijing 100053, Peoples R China
[2] Capital Med Univ, Xuanwu Hosp, Dept Pathol, Beijing 100053, Peoples R China
[3] Capital Med Univ, Xuanwu Hosp, Dept Radiol, Beijing 100053, Peoples R China
[4] Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing 100053, Peoples R China
关键词
epilepsy; dysembryoplastic neuroepithelial tumor; magnetic resonance imaging; magnetic resonance spectroscopy; MR SPECTROSCOPY; BRAIN; EPILEPSY;
D O I
10.3760/cma.j.issn.0366-6999.2009.20.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Dysembryoplastic neuroepithelial tumor (DNT) is a rare benign neoplasm of the central nervous system affecting young people. A correct preoperative diagnosis is helpful for planning surgical strategies and improving prognosis. The purpose of this study was to characterize DNTs using magnetic resonance imaging (MRI) and magnetic resonance spectroscopy (MRS) and to analyze the value of these two techniques in the diagnosis of DNTs. Methods MR images of 13 patients with DNTs were reviewed retrospectively; and five of the patients also underwent MRS. Tumors were confirmed by surgery. The distribution, extension and signal features of the lesions were assessed, and the MRS results were analyzed. Results All tumors were supratentorial. The cortex was the main area involved, with nine tumors located in the temporal lobe, three in the frontal lobe, and one on the boundary between the temporal and occipital lobes. All cases had decreased signal intensity on T1-weighted MR images and increased signal intensity on T2-weighted images. On fluid attenuated inversion recovery weighted images, the hyperintense "ring sign" and internal septation of the lesion were seen in 9 cases. Eight tumors had well-demarcated borders. Peritumoral edema or mass effect was absent in all cases. A contrast enhancement examination was performed in 9 cases. Contrast enhancement was absent in five cases, and four cases showed significant enhancement. The MRS showed a low N-acetylaspartate peak and a lack of elevated choline-containing component (Cho) or Cho-Cr ratio (Cho/Cr) in five patients. Conclusions The MRI findings of DNTs were stereotypical. The combination of MRI and MRS techniques were helpful in making a correct presurgical diagnosis. Chin Med J 2009;122(20):2433-2437
引用
收藏
页码:2433 / 2437
页数:5
相关论文
共 20 条
[1]  
[安维民 AN Weimin], 2006, [中国医学影像学杂志, Chinese Journal of Medical Imaging], V14, P259
[2]   Simple and complex dysembryoplastic neuroepithelial tumors (DNT) variants: clinical profile, MRI, and histopathology [J].
Campos, Alexandre R. ;
Clusmann, Hans ;
von Lehe, Marec ;
Niehusmann, Pitt ;
Becker, Albert J. ;
Schramm, Johannes ;
Urbach, Horst .
NEURORADIOLOGY, 2009, 51 (07) :433-443
[3]  
Cosson RS, 2001, J NEURORADIOLOGY, V28, P230
[4]  
Daumas-Duport C, 2000, PATHOLOGY GENETICS T, P103
[5]   DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMORS [J].
DAUMASDUPORT, C .
BRAIN PATHOLOGY, 1993, 3 (03) :283-295
[6]   DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR - A SURGICALLY CURABLE TUMOR OF YOUNG-PATIENTS WITH INTRACTABLE PARTIAL SEIZURES - REPORT OF 39 CASES [J].
DAUMASDUPORT, C ;
SCHEITHAUER, BW ;
CHODKIEWICZ, JP ;
LAWS, ER ;
VEDRENNE, C .
NEUROSURGERY, 1988, 23 (05) :545-556
[7]  
Fernandez C, 2003, AM J NEURORADIOL, V24, P829
[8]   1H MR spectroscopy of brain tumours and masses [J].
Howe, FA ;
Opstad, KS .
NMR IN BIOMEDICINE, 2003, 16 (03) :123-131
[9]   DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR - A TUMOR WITH SMALL NEURONAL CELLS RESEMBLING OLIGODENDROGLIOMA [J].
LEUNG, SY ;
GWI, E ;
NG, HK ;
FUNG, CF ;
YAM, KY .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1994, 18 (06) :604-614
[10]   Surgical strategies and seizure control in pediatric patients with dysembryoplastic neuroepithelial tumors: a single-institution experience [J].
Minkin, Krasimir ;
Klein, Olivier ;
Mancini, Josette ;
Lena, Gabriel .
JOURNAL OF NEUROSURGERY-PEDIATRICS, 2008, 1 (03) :206-210