AIDS-Related Central Nervous System Toxoplasmosis With Increased 18F-Fluoroethyl-L-Tyrosine Amino Acid PET Uptake Due to LAT1/2 Expression of Inflammatory Cells.

Clin Nucl Med

From the *Department of Neurology 1, NeuroMed Campus, Kepler University Hospital, Linz, Austria; †Department of Neurology, ‡Wilhelm Sander Neurooncology Unit, and Departments of §Neuropathology and ∥Nuclear Medicine, University of Regensburg Medical School, Regensburg; ¶Institute of Neuroscience and Medicine, Forschungszentrum Jülich, Jülich; **Department of Neurology, University of Cologne, Cologne; ††Center of Integrated Oncology, Universities of Cologne and Bonn, Cologne; and ‡‡Department of Nuclear Medicine, University of Aachen, Aachen, Germany.

Published: December 2017

We report the case of a 40-year-old woman with a progressive right-sided hemiparesis. Standard MRI revealed a contrast-enhancing brain lesion within the left basal ganglia. Ffluoroethyl-L-tyrosine (F-FET) PET showed a distinct tracer uptake (lesion-to-brain ratio [LBR]: LBRmax = 2.03, LBRmean = 1.68) with a significant larger metabolic lesion volume than contrast-enhancement in MRI, indicating cerebral glioma. Surprisingly, histopathologic analysis demonstrated central nervous system toxoplasmosis with pronounced inflammatory reaction (reactive astrogliosis, microglia activation, macrophage, and T-lymphocyte infiltration), which was associated with strong LAT1/LAT2/CD98 expression. In conclusion, inflammatory brain lesions, such as cerebral toxoplasmosis, represent a potential pitfall of F-FET PET mimicking a brain tumor.

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http://dx.doi.org/10.1097/RLU.0000000000001873DOI Listing

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