Pediatric low-grade gliomas: Prognosis with proton magnetic resonance spectroscopic imaging

被引:32
作者
Lazareff, JA
Bockhorst, KHJ
Curran, J
Olmstead, C
Alger, JR
机构
[1] Univ Calif Los Angeles, Sch Med, Div Neurosurg, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Surg, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Radiol Sci, Los Angeles, CA 90095 USA
关键词
brain; low-grade glioma; magnetic resonance spectroscopy; prognosis; tumor;
D O I
10.1097/00006123-199810000-00053
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: Our aim was to assess the correlation between the low-grade glioma (LGG) metabolic profile and tumor progression. Using in vivo proton magnetic resonance spectroscopic imaging, we specifically asked whether and which metabolic features are associated with tumor regrowth or recurrence. METHODS: Eleven pediatric patients with histologically proven partially resected (<20% resection) midline LGG were treated and followed up for a period of 2 years. All patients underwent proton magnetic resonance spectroscopic imaging studies before any management was determined. Tumor progression was defined as radiological evidence of mass enlargement (>25%) during the follow-up period. Proton magnetic resonance spectroscopic imaging was performed using a PRESS-CSI sequence on a General Electric 1.5-tesla scanner (General Electric Medical System, Waukesha, WI). The signal intensities of N-acetylaspartate, choline (CHO), and creatine from the tumor and the normal brain were used to calculate normalized metabolite intensities and metabolite ratios. RESULTS: Tumors that progressed during a 2-year period displayed higher normalized CHO than those that remained stable (Mann-Whitney test, P < 0.03). The majority (five of six) of the rapidly growing LGG showed values of normalized CHO of at least 1, whereas the nonprogressors had a normalized CHO value of less than 1. CONCLUSION: In association with pediatric LGG, high normalized CHO values seem to herald the potential for rapid tumor growth. These observations may be valuable for defining subsets of patients with LGG who may benefit from early therapeutic interventions.
引用
收藏
页码:809 / 817
页数:9
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