EVALUATION OF FLUORODEOXYGLUCOSE-POSITRON EMISSION TOMOGRAPHIC SCANNING AND ITS ASSOCIATION WITH GLUCOSE-TRANSPORTER EXPRESSION IN MEDULLARY-THYROID CARCINOMA AND PHEOCHROMOCYTOMA - A CLINICAL AND MOLECULAR STUDY
Tj. Musholt et al., EVALUATION OF FLUORODEOXYGLUCOSE-POSITRON EMISSION TOMOGRAPHIC SCANNING AND ITS ASSOCIATION WITH GLUCOSE-TRANSPORTER EXPRESSION IN MEDULLARY-THYROID CARCINOMA AND PHEOCHROMOCYTOMA - A CLINICAL AND MOLECULAR STUDY, Surgery, 122(6), 1997, pp. 1049-1060
Background, Imaging of metastatic sites of medullary thyroid carcinoma
(MTC) is successful in less than 60% of cases of residual or recurren
t disease. Positron emission tomography (PET) with [F-18]fluoro-2-deox
y-D-glcose (FDG) takes advantage of the fact that malignant tumors are
capable of increased uptake and use of glucose, which is mediated by
the members of the glucose transporter family of proteins (GLUT 1 thro
ugh GLUT 5). Methods. FDG-PET images of 10 patients with recurrent or
persistent MTC after primary operation were compared with images by co
mputed tomography or magnetic resonance imaging. Identified metastatic
lesions were assessed by intraoperative findings and pathology report
s. Expression of GLUT 1 through GLUT 5 was examined by Western blot an
alysis of tumor tissue from eight of the patients evaluated and an add
itional panel of 10 MTCs and seven pheochromocytomas. Results. FDG-PET
identified 31 foci of FDG accumulation in 10 patients, and 16 of thes
e metastatic sites were resected and confirmed by histologic analysis.
Only 11 foci were demonstrated by computed tomographic or magnetic re
sonance imaging. None of the glucose transporters examined displayed s
ignificant expression. Two pheochromocytomas were successfully imaged
by FDG-PET. Conclusions, FDG-PET imaging can be useful in the localiza
tion of cervicomediastinal MTC metastases and pheochromocytoma. The In
creased glucose uptake in these tumors, as evidenced by FDG-PET, does
not appear to be attributable to the expression of the glucose transpo
rter proteins GLUT 1 through GLUT 5.