Questions | Answers |
1. What is the physiologic principle behind blood-brain barrier imaging? | 1. Tracers stay within the blood pool and diffuse into the brain only when the blood-brain barrier is disrupted. |
2. What three tracers are used for blood-brain barrier imaging? | 2. 99mTc-pertechnetate, 99mTc-DTPA, and 99mTc-glucoheptonate |
3. What is the main disadvantage of 99mTc-pertechnetate for blood-brain barrier imaging? | 3. It localizes physiologically in the choroid plexus. |
4. Why does 99mTc-glucoheptonate have better uptake in brain tumors than other blood-brain barrier imaging agents? | 4. As a glucose analog, it may serve as a substrate for tumor metabolism. |
5. How do corticosteroids affect blood-brain barrier imaging? | 5. They may diminish uptake, because corticosteroids decrease the permeability of the blood-brain barrier. |
6. How is blood-brain barrier imaging performed? | 6. Blood flow images are taken every two to three seconds for one minute, then 750K count immediate static images are taken in multiple views, and then, 1.5 to 2 hours later, 750K count delayed static images are obtained in multiple views. |
7. On blood-brain barrier imaging, how much uptake is present in the healthy brain? | 7. none |
8. What structures are seen only on blood-brain barrier imaging? | 8. the scalp and venous sinuses |
9. What are the findings of subdural hematoma on blood-brain barrier imaging? | 9. peripherally reduced flow on dynamic images, with increased up-take on delayed images |
10. What are the findings of a ventriculitis on blood-brain barrier imaging? | 10. bilaterally increased uptake in the region of the lateral ventricles |
11. What are the findings of an abscess on blood-brain barrier imaging? | 11. a focal area of increased uptake on delayed imaging, with a cold center developing as the abscess progresses |
12. What are the findings of herpes encephalitis on blood-brain barrier imaging? | 12. increased flow and uptake in the affected temporal lobe |
13. What is the characteristic finding of an infarct on the angiogram portion of a blood-brain barrier scan? | 13. reduced early perfusion with increased delayed perfusion; these symptoms are known as the “flip-flop” phenomenon |
14. How long after an infarct is the “flipflop” perfusion first seen on blood-brain barrier imaging? | 14. in the first few days |
15. What is “luxury perfusion”? | 15. increased blood flow to an infarction due to uncoupling of metabolism, typically seen about five days after an infarction |
16. What is the best tracer to use to diagnose venous sinus thrombosis? | 16. 99mTc-RBCs |
17. What is the typical finding of venous sinus thrombosis in 99mTc–red blood cell (RBC) imaging? | 17. abrupt termination of the midportion of sinus |
18. What are the findings of an arteriovenous malformation on brain imaging with 99mTc-RBCs? | 18. intense uptake on delayed images |
19. What is the advantage of radionuclide angiography over the electroencephalogram (EEG) in confirming brain death? | 19. radionuclide angiography remains accurate in the face of hypothermia and drug intoxication |
20. What are the scintigraphic criteria for brain death on a radionuclide angiogram? | 20. presence of a good carotid bolus without intracranial arterial flow |
21. What is the significance of faint visualization of the venous sagittal sinus or the transverse sinus on radionuclide angiography to confirm brain death? | 21. It may be seen in 10% to 20% of patients with brain death and does not preclude the diagnosis of brain death, so long as there is no intracranial arterial flow. |
22. What are the common features of tracers for imaging regional cerebral perfusion? | 22. They are small, neutral lipophilic molecules; they rapidly diffuse across the blood-brain barrier; they have a high brain extraction fraction; and they remained fixed in the brain. |
23. What three tracers are available for cerebral perfusion scintigraphy? | 23. 123I-isopropyl iodo-amphetamine (IMP), 99mTc–hexamethyl propylene amine oxime (HMPAO), and 99mTc–ethylcysteine dimer (ECD) |
24. What percentage of a dose of 123IIMP (isopropyl iodo-amphetamine) localizes in the healthy brain? | 24. 6% to 9% |
25. 3–6 mCi (111–222 MBq) | |
26. What is the main difference between 123I-IMP and 99mTc-HMPAO (hexamethyl propylene amine oxime) in brain uptake distribution? | 26. 123I-IMP demonstrates redistribution that is independent of brain-blood flow. |
27. What is the ratio of gray-to-white matter uptake with 123I-IMP? | 27. 3–4:1 |
28. What percentage of a dose of 99mTcHMPAO localizes in the normal brain? | 28. 3.5% to 7% |
29. What is the ratio of gray-to-white matter uptake with 99mTc-HMPAO? | 29. 2.5:1 |
30. How do images of 123I-IMP and 99mTcHMPAO differ when imaging infarction? | 30. 123I-IMP always shows a flow defect; 99mTc-HMPAO may show luxury per-fusion with increased uptake. |
31. How long after injection of 99mTcHMPAO does peak brain uptake occur? | 31. two minutes |
32. What percentage of a dose of 99mTcECD (ethylcysteine dimer) localizes in the healthy brain? | 32. 6% to 7% |
33. How long after injection of 99mTc-ECD does peak brain uptake occur? | 33. two minutes |
34. How do 99mTc-HMPAO and 99mTc-ECD differ in terms of blood pool clearance? | 34. Blood pool clearance is faster with 99mTc-ECD. |
35. How do the circumstances of injection affect cerebral perfusion imaging? | 35. Stimulation (e.g., visual or auditory) during the injection can cause areas of increased uptake in the site stimulated. |
36. What type of image acquisition is required for cerebral perfusion imaging? | 36. SPECT acquisition |
37. What is the normal cerebral blood flow in an adult? | 37. approximately 50 mL/min/100 g |
38. What is the normal cerebral blood flow in a 3- to 10-year-old child? | 38. approximately 100 mL/min/100 g |
39. How does blood flow change in the occipital lobes when the eyes are open versus when they are closed? | 39. Blood flow increases by approximately 30%. |
40. How does an intraictal seizure focus affect regional cerebral blood flow? | 40. It causes an increase in blood flow. |
41. What practical methods are available to quantify absolute regional cerebral blood flow with single-photon emission computed tomography (SPECT)? | 41. none |
42. PET imaging with 15O water, or 15C carbon dioxide, or 133Xe imaging with a multiprobe detector | |
43. What is the critical organ and what is its radiation dose for 123I-IMP? | 43. the lung, with 0.84 rads (8.4 mGy)/6 mCi (222 MBq) |
44. What is the critical organ and what is its radiation dose for 99Tc-HMPAO? | 44. the lacrimal glands, with 5.2 rads (52 mGy)/20 mCi (740 MBq) |
45. How long after infarction will decreased blood flow be seen on a cerebral perfusion scan? | 45. immediately |
46. In patients with cerebral infarcts, why are defects on cerebral perfusion images often larger than on computed tomography (CT) scans? | 46. the area of infarction is surrounded by an ischemic area of decreased blood flow |
47. What is the cause of crossed cerebellar diaschisis? | 47. Increased activity in the cerebellum contralateral to a cerebral infarction is due to increased blood flow to the cerebellum after a loss of suppressive neural activity from the contra-lateral cortex. |
48. Which two factors decrease the sensitivity of cerebral perfusion imaging for infarctions? | 48. luxury perfusion, and difficulty detecting lacunar infarcts |
49. True or false: 180-degree acquisitions on 99Tc-HMPAO studies are diagnostically comparable to 360-degree acquisitions. | 49. false |
50. What is the typical scintigraphic pattern of Alzheimer disease on cerebral perfusion imaging? | 50. bilateral posterior temporal and parietal hypoperfusion |
51. What is the typical scintigraphic pattern of Pick disease on cerebral perfusion imaging? | 51. bilateral frontal hypoperfusion |
52. What is the typical scintigraphic pattern of multi-infarct dementia on cerebral perfusion imaging? | 52. multiple asymmetric perfusion defects involving both the cortex and deep structures |
53. What is the positive predictive value of brain perfusion scintigraphy for Alzheimer disease? | 53. approximately 80% |
54. What is the typical scintigraphic pattern of depression on cerebral perfusion imaging? | 54. normal perfusion |
55. What is the typical scintigraphic pattern of metabolic brain dysfunction on cerebral perfusion imaging? | 55. normal perfusion |
56. What is the typical scintigraphic pattern of Huntington chorea on cerebral perfusion imaging? | 56. reduced perfusion of the caudate nucleus |
57. What is the typical scintigraphic pattern of AIDS dementia on cerebral perfusion imaging? | 57. multifocal or patchy cortical and subcortical regions of hypoperfusion |
58. What is the typical scintigraphic pattern of an interictal seizure focus on cerebral perfusion imaging? | 58. hypoperfusion |
59. What is the typical scintigraphic pattern of an ictal seizure focus on cerebral perfusion imaging? | 59. hyperperfusion |
60. What is the sensitivity of brain per-fusion SPECT for the detection of interictal seizure foci? | 60. approximately 65% to 75% |
61. What is the relative sensitivity of brain perfusion SPECT for the detection of the ictal versus interictal seizure foci? | 61. The sensitivity is greater for ictal foci. |
62. How is brain perfusion SPECT useful in conjunction with the Wada test? | 62. Brain perfusion SPECT can demonstrate the exact territory perfused by the pentobarbital. |
63. How is 201Tl imaging useful for the assessment of brain tumors? | 63. The degree of the 201Tl uptake is proportional to the malignant grade of the tumor, and uptake in the brain distinguishes recurrent brain tumor from radiation necrosis. |
64. How is 201Tl imaging useful for the assessment of AIDS patients with intracerebral mass lesions? | 64. The 201Tl uptake indicates the presence of brain tumors such as lymphoma; absence of 201Tl uptake indicates the presence of infection, such as toxoplasmosis. |
65. Which tracer is currently used for radionuclide cisternography? | 65. intrathecal 111In-DTPA |
66. What is the critical organ, and its radiation dose, for intrathecal 111InDTPA? | 66. the surface of the spinal cord, with 5 rads (50 mGy)/0.5 mCi (18.5 MBq) |
67. How can radionuclide cisternography distinguish normal-pressure hydrocephalus from cerebral atrophy? | 67. Cisternography will show prolonged ventricular uptake in normal-pressure hydrocephalus. |
68. How is radionuclide cisternography used for the detection of cerebrospinal fluid (CSF) leaks? | 68. Imaging to visualize leaked radioactivity; pledgets placed in the nasal cavity and counted for the leaked radioactivity. |
69. True or false: In the initial stage of cerebral ischemia, regional cerebral blood flow (rCBF) increases. | 69. false |
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