Combined use of F-18 fluorocholine positron emission tomography and magnetic resonance spectroscopy for brain tumor evaluation

被引:40
作者
Kwee, SA [1 ]
Coel, MN [1 ]
Lim, J [1 ]
Ko, JP [1 ]
机构
[1] Queens Med Ctr, Dept Nucl Med, Hamamatsu Queens PET Imaging Ctr, Honolulu, HI 96813 USA
关键词
brain tumor; neoplasm; positron emission tomography; magnetic resonance spectroscopy; fluorocholine;
D O I
10.1177/1051228404264957
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background. Choline metabolism is often abnormal in malignant brain tumors. Methods. Brain positron emission tomography (PET) imaging with F-18 fluorocholine (FCH) was performed on 2 patients with intracranial lesions suspected to be high-grade malignant gliomas on the basis of magnetic resonance (MR) imaging and multivoxel 1H-MR spectroscopic imaging (MRSI) findings. Standardized uptake value (SUV) measurements on PET were compared with measurements of choline/creatine metabolite ratio on MRSI in corresponding regions. Brain biopsy revealed glioblastoma multiforme (GBM) in one case and demyelinating disease in the other. Results. In the case of GBM, the tumor demonstrated increased FCH uptake on PET. The mean and maximum SUV in areas of the tumor correlated with regional choline/creatine ratio measurements (r = 0.76, P <.001; r = 0.83, P <.001, respectively). In the case of tumefactive demyelinating lesions, the lesion demonstrated low FCH uptake, which did not correlate with choline/creatine ratio measurements. Conclusions. Assessments of choline metabolism may aid in evaluating intracranial mass lesions.
引用
收藏
页码:285 / 289
页数:5
相关论文
共 34 条
  • [1] Aboagye EO, 1999, CANCER RES, V59, P80
  • [2] Bitsch A, 1999, AM J NEURORADIOL, V20, P1619
  • [3] THE PROTON NMR-SPECTRUM IN ACUTE EAE - THE SIGNIFICANCE OF THE CHANGE IN THE CHO-CR RATIO
    BRENNER, RE
    MUNRO, PMG
    WILLIAMS, SCR
    BELL, JD
    BARKER, GJ
    HAWKINS, CP
    LANDON, DN
    MCDONALD, WI
    [J]. MAGNETIC RESONANCE IN MEDICINE, 1993, 29 (06) : 737 - 745
  • [4] Coleman, 2000, Clin Positron Imaging, V3, P147, DOI 10.1016/S1095-0397(00)00059-5
  • [5] Sequential proton MRS study of brain metabolite changes monitored during a complete pathological cycle of demyelination and remyelination in a lysophosphatidyl choline (LPC)-induced experimental demyelinating lesion model
    Degaonkar, MN
    Khubchandhani, M
    Dhawan, JK
    Jayasundar, R
    Jagannathan, NR
    [J]. NMR IN BIOMEDICINE, 2002, 15 (04) : 293 - 300
  • [6] DeGrado TR, 2001, J NUCL MED, V42, P1805
  • [7] GEORGE TP, 1991, J BIOL CHEM, V266, P12419
  • [8] MULTIPLE-SCLEROSIS MASQUERADING AS A MASS LESION
    GIANG, DW
    PODURI, KR
    ESKIN, TA
    KETONEN, LM
    FRIEDMAN, PA
    WANG, DD
    HERNDON, RM
    [J]. NEURORADIOLOGY, 1992, 34 (02) : 150 - 154
  • [9] Hara T, 1997, J NUCL MED, V38, P842
  • [10] Use of 18F-choline and 11C-choline as contrast agents in positron emission tomography imaging-guided stereotactic biopsy sampling of gliomas
    Hara, T
    Kondo, T
    Hara, T
    Kosaka, N
    [J]. JOURNAL OF NEUROSURGERY, 2003, 99 (03) : 474 - 479