Seminars Flashcards
Extrapyramidal definition
corticospinal motor pathways (pyramidal projections) are not the primary site(s) of dysfunction
PSP
Bradykinesia/rigidity, supranuclear ocular palsy
FDG: Decrased striatum
DATSCAN: symmetric defects
No Lewy Body’s, TAU positive
MSA
Autonomic dysfunction
FDG: Decfreased striatum
DATSCAN: Symmetric defects
Corticobasilar degeneration
Dystonia, myoclonis, alien limb
FDG: Decreased precentral and post central gyri, decreased striatum, decreased thalamus
DATSCAN: assymetric reduction
Parkinson’s features
FDG: increased striatum (early stages)
I123-ioflupane (DATSCAN) - assymetric defect putamen > caudate
Lewy body deposition
Protein deposition in LBD
All have alpha-Syn protein deposition; subset have beta amyloid and tau (overlap with AD)
3 Pillars of drug survival
tissue exposure
target engagement
pharmacologic activity
NeuroPET targers
Dopamine:
- D1, D2/D3 (C11-raclopride), DAT (I123-Ioflupane), 5-L AA transporter (DOPA)
Seratonin:
- 5HT receptor agonists/antagonists
Opiod:
- u opiod receptor agonist - C11-carfentanyl
GABA
- GABA receptor antagonist (C11-flumazenil)
Beta amyloid -
- C11PIB
- F18-flurbetapir
Combined beta amyloid and neurofibrillary tangles:
- F18-FDDNP
Appropriate use amyloid PET
- Cognitive complaint with objectively confirmed impairment
- AD is a possible diagnosis, but diagnosis is uncertain after a comprehensive evaluation
- Knowledge of the presence or absence of Aβ pathology will aid diagnosis or management
- Persistent or progressive unexplained MCI
- Possible AD with an unclear clinical presentation (see text)
- Atypically early-age-onset progressive dementia (less than ~65 y in age)
PET tracers being used for gliomas
C11-MET
C11-AMT
F18-FET
F18-DOPA
PET findings in addiction
low striatal D2 receptors and dopamine transmission
Applications of beta amyloid imaging and tau
Noninvasive identification of Alzheimer disease pathology
Early diagnosis
Prediction of disease progression and response to disease-specific therapy
Subject selection for disease-specific trials
Monitor target engagement and effectiveness of disease-specific therapy
Tau tracers
F18-AV1451
Dosimetry before I131 therapy in children
Measure RAIU with < 10-15 MBq of I131 or I124 PET to avoid stunning
Two neurocutaneous syndromes with epilepsy ammendable to surgical treatment
TS
Sturge-Weber (angiomatosis, calcifictions, atrophy, gliosis)
Children - differences in MIBI and tetrofosmin biodistribution
Higher hepatic retention - do delayed at 90 min
Sp I123 and 131-MIBG
Specificity between 90-100%
PET tracers for NB
F18-FDG
F18-DOPA
Ga68-DOTATATE
BEIR statement on radiation carcinogenic risk in children
2-3 x higher than adults
ICRP Effective Dose Organ radiosensitivity weights
- 12 = Breast, Red Marrow, Lung, Colon, Stomach
- 08 = gonads
Lowest = 0.01 (brain, bone surface, salivary glands)
Rank effective dose (mSv) for the following studies: DMSA, MDP, MAG3, FDG
FDG (7.0) > MDP (4.2) > MAG3 (2.6) > DMSA (1.1)
Most common cause congenital hypothyroidism
Thyroid dysgenesis
ROME consensus for imaging in congenital hypothyroidismn
Knee radiographs (absent femoral and tibial epiphyses) reflect severity of hypothyroidism
Thyroid US
Thyroid scintigraphy
Timing of scintigraphy for CH and initiation of L-thyroxine
Imaging must be done within a week of beginning therapy
Protocol for congenital hypo
Prep: ensure < 1 week since starting therapy
Tracer: I123 - 0.03 mCi, image after 1 hour; Tc99m - 0.11-0.22 mCi, image after 15 minutes
Dose: I123 - 3.6 mSv; Tc99m - 1.2 mSv
Collimator: LEHR
Matrix: 128 x 128
FOV: anterior acquisition of trunk
Milk scan protocol
Prep - 4-6 hr fast
Tracer: 0.25 mCi Tc99m-SC
Position: Supine; posterior images
Matrix: 128 x 128, 5-10s vs 30s frames x 60 minutes, then static chest with 256 x 256 matrix
FOV: mouth to upper abdomen
Critical organ - lower large bowel
Salivagram protocol
Prep: None
Tracer: 0.3 mCi Tc99m-SC
LEHR collimator, 128 x 128, dynamic 60min 30s frames, then static A and P chest at 256 x 256 for 3-5 min
Dose reduction strategies pediatric PET/CT
- Eliminate unnecessary tests
- Reduce dose of tracer
- Reduce CT imaging params - decrase mAs, kvp; Incrase pitch; use dose modulation
- Reduce area imaged
- Choose appropriate CT - diagnostic vs non-diagnostic
Pediatric MDP dose and timing
0.25 mCi/kg, image at 2-4 hrs
Main advantage of direct RNC vs indirect
Both the filling and micturition phases assessed, increasing sensitivity of study
Expected bladder capacity for age
30 + (30*age in yrs)
International Reflux grading system
1 = Contrast refluxes into normal sized ureter
2 = Contrast reflues into non-dilated ureter and pelvicalyceal system
3 = Mild hydronephrosis, sharp angle of fornices blunted
4 = Moderate dilatation with distortion of fornices
5 = severe dilatation, tortuosity of ureter, clubbing of calyces
Techniques for Crohn’s imaging
- WBC scintigraphy - extent of active disease; differentiates inflammatory from fibrotic strictures
- FDG-PET - Non-specific pan-inflammatory marker; high radiation dose
- FDG PET-MRI -
Nuc medicine tracers for type 1 diabetes
F18-DOPA - quantifying functional beta cell mass
Radiolabeled IL-2 - Uptake correlates with duration of disease
Classic Hodgkin’s lymphoma classification
- Nodular sclerosing
- Mixed cellularity
- Lymphocyte rich
- Lymphocyte depleted
PET tracers for imaging bone marrow
- F18-FDG (glucose metabolism)
2. F18-FLT (DNA proliferation)
SPECT tracers for imaging bone marrow
- Tc-SC (RES)
- Tc-nannocolloid (RES)
- Tc/In111-WBCs - RES/neutrophils
Dual time point imaging (DTPI)
Malignant lesions tend to accumulate FDG more than normal tissues, therefore higher target to background on delayed
Benign bone/soft tissues lesions with high FDG uptake (false positives)
Hibernoma Sarcoid Myosotis ossificans Infection \+ Bone lesions (osteoid osteoma, GCT, enchondroma)
Malignant bone/soft tissue lesions with low FDG uptake (false negative)
well diff liposarc
myxoid liposarc
chondrosarcoma
chordoma
PET findings relapsing polychondritis
Auricular, nasal, larynx, tracheal chondritis
Bronchial chondritis
Relapsing polychondritis
3 major types of aggregated amyloid proteins
- beta amyloid
- Tau
- alpha-synuclein (alpha-syn)
Desired amyloid PET properties
- Selectively binds amyloid
- Crosses BBB
- No radiolabeled metabolites in brain
Venn diagram aggregated amyloid proteins
- Pure beta amyloid = cerebral amyloid angiopathy
- Pure tau = Frontotemporal dementia, CBD, PSP
- Pure alpha-syn = PD, DLB, MSA
- Beta amyloid + tau = AD
- All 3 = Lewy Body variant AD
Radiolabeled peptide definition
Between small molecules and large biologics
Eg. SSTRs, PSMA
C11 production
N14(p,alpha)C11