“…In contrast to the study of Launes et al [9] the present in vivo experiments, using an animal model, reveal no significant difference in brain uptake of HM-PAO between infected and non-infected animals (Fig. 1).…”
Selective uptake of the cerebral blood-flow imaging agent 99mTc-hexamethylpropyleneamine oxime (HM-PAO) by Human Herpesvirus 1 (HSV-1) infected cells was investigated in vivo and in vitro. No specific uptake of HM-PAO was observed either in encephalitic rats (by brain scintigraphic imaging or by immunoperoxidase staining/autoradiography of brain sections) or in HSV-1 infected Vero cells.
“…In contrast to the study of Launes et al [9] the present in vivo experiments, using an animal model, reveal no significant difference in brain uptake of HM-PAO between infected and non-infected animals (Fig. 1).…”
Selective uptake of the cerebral blood-flow imaging agent 99mTc-hexamethylpropyleneamine oxime (HM-PAO) by Human Herpesvirus 1 (HSV-1) infected cells was investigated in vivo and in vitro. No specific uptake of HM-PAO was observed either in encephalitic rats (by brain scintigraphic imaging or by immunoperoxidase staining/autoradiography of brain sections) or in HSV-1 infected Vero cells.
“…These have demonstrated abnormally increased tracer uptake in the acutely affected temporal lobe [2][3][4][5][6]. However, the PET metabolism pattern of elevated uptake is somewhat different from the SPECT perfusion pattern.…”
This first known positron emission tomography report on metabolic changes in acute herpes simplex virus (HSV-1) encephalitis demonstrates focal hypermetabolism in areas of cerebral cortex adjacent to actively inflamed hippocampus acutely infected with HSV-1. When neuropsychiatric symptoms recurred in a previously healthy 61-year-old patient 1 month after recovering from acute HSV-1 encephalitis, repeat positron emission tomography with fluorodeoxyglucose was helpful in ruling out recurrent active infection by showing marked hypometabolism throughout the previously infected temporal lobe.
“…We ruled out neurological disorders associated with cerebral hypermetabolism on FDG-PET such as high-grade glioma [1,2], herpes simplex encephalitis [3] and seizure [4,5]. There have been two reports in which FDG-PET scan, obtained in the acute stage of LE, demonstrated hypermetabolic foci in the medial temporal lobe [6,7].…”
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