CONTRIBUTION OF MAGNETIC-RESONANCE SPECTROSCOPIC IMAGING AND L-[1-C-11]TYROSINE POSITRON EMISSION TOMOGRAPHY TO LOCALIZATION OF CEREBRAL GLIOMAS FOR BIOPSY
Kg. Go et al., CONTRIBUTION OF MAGNETIC-RESONANCE SPECTROSCOPIC IMAGING AND L-[1-C-11]TYROSINE POSITRON EMISSION TOMOGRAPHY TO LOCALIZATION OF CEREBRAL GLIOMAS FOR BIOPSY, Neurosurgery, 34(6), 1994, pp. 994-1002
PROTON MAGNETIC RESONANCE spectroscopic imaging (H-1-MRSI) and positro
n emission tomography with the tracer L-[1-C-11]tyrosine (C-11-TYR) we
re used to localize gliomas for biopsy or resection. This is especiall
y helpful in cases of low-grade gliomas, if these lesions are not visu
alized by contrast-enhanced computed tomographic and magnetic resonanc
e imaging scans. The clues to improved localization are provided by ch
anges in tissue metabolite contents, such as elevation of phosphocholi
ne, indicating cellular proliferation; decrease of N-acetylaspartate,
denoting toss of neurons (as these are replaced by tumor cells); and e
levation of lactate, pointing to the prevalence of glycolysis, as obse
rved in many tumors. These data on tissue metabolite content have been
obtained in vivo in the patient by proton magnetic resonance spectros
copy; metabolite maps derived from these data then visualize the distr
ibution of the various metabolites over the section of the brain under
investigation. Alternatively, localization of a tumor may be achieved
by means of positron emission tomography depicting the pattern of upt
ake of the amino acid tracer C-11-TYR, as it tends to be incorporated
in the process of cellular proliferation and protein biosynthesis. Fiv
e cases are presented as examples.