12. Application of FDG PET-CT in non-oncological diseases - neurology, cardiology and unclear febrile conditions.
Covers FDG PET/CT in neurology, first explaining normal brain uptake and then patterns in dementia (Alzheimer, frontotemporal, Lewy body and vascular), epilepsy with interictal and ictal findings, and parkinsonian syndromes. It then addresses cardiac viability, contrasting perfusion-metabolism matches and mismatches with a summary table and patient glucose preparation, and closes with fever of unknown origin, covering causes such as vasculitis, osteomyelitis and sarcoidosis and the use of PET-guided biopsy.
Topic 12 of 50 in the MU Sofia syllabus for Nuclear Medicine (Medicine, Year 4). The free AceMed note covers it in 16 sections, about 1,416 words (10 min of reading), with 16 flashcards.
In this note
NEUROLOGICAL INDICATIONS
CARDIOLOGICAL INDICATIONS
INFECTION AND INFLAMMATION INDICATIONS
Application of FDG PET-CT in non-oncological diseases - neurology, cardiology and unclear febrile conditions.
PART I — FDG PET/CT IN NEUROLOGY
Why does hypometabolism occur?
Frontotemporal Dementia
Dementia with Lewy Bodies
Vascular Dementia
Epilepsy
Interictal FDG PET
Movement Disorders
Brain Tumor Follow-Up as a Neurological Application
PART II — FDG PET/CT IN CARDIOLOGY
Myocardial Viability
PART III — FEVER OF UNKNOWN ORIGIN
NEUROLOGICAL INDICATIONS
1. Epilepsy
Interictal FDG PET may show: Reduced metabolism at the epileptic focus It is useful in patients being assessed for epilepsy surgery.
2. Dementia
Characteristic metabolic patterns may help differentiate:
Alzheimer disease
Frontotemporal dementia
Dementia with Lewy bodies
Alzheimer Disease
Typical reduction in metabolism in:
Temporoparietal cortex
Posterior cingulate cortex
Precuneus
Frontotemporal Dementia
Reduced metabolism mainly in:
Frontal lobes
Anterior temporal lobes
Dementia with Lewy Bodies
Often shows:
Occipital hypometabolism
Relative preservation of posterior cingulate activity in some cases
3. Brain Tumors
FDG has limitations because normal brain cortex already has high glucose metabolism.
Other PET tracers such as amino-acid tracers may be more useful in selected brain tumors.
PET can help assess:
Tumor recurrence
Viable tumor
Treatment response
Differentiation from radiation necrosis
4. Movement Disorders
Receptor or transporter PET tracers can assess:
Dopamine synthesis
Dopamine receptor function
Parkinsonian syndromes
CARDIOLOGICAL INDICATIONS
1. Myocardial Viability
FDG PET evaluates glucose metabolism in myocardium.
A region with:
Reduced perfusion
Preserved FDG uptake
may represent viable but dysfunctional myocardium.
This is called a: Perfusion-metabolism mismatch
Such myocardium may recover after revascularization.
2. Myocardial Perfusion
Tracers such as:
13N-ammonia
15O-water
Rubidium-82
can be used for quantitative myocardial perfusion imaging.
Special dietary preparation may be required to suppress normal myocardial glucose uptake.
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