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Title: Brant and Helms Chapters 5963: Nuclear Medicine


1
Brant and HelmsChapters 59-63Nuclear Medicine
  • Christopher Sherman

2
Outline
  • Cerebrovascular System
  • Thyroid Imaging and Uptake
  • Gastrointestinal Tract
  • Genitourinary System
  • Inflammation and Infection Imaging
  • Conventional Neoplasm Imaging

3
Cerebrovascular System
  • Radionuclide Brain Imaging
  • Planar Brain Imaging
  • SPECT Brain Perfusion Imaging

4
Planar Brain Imaging
  • Only performed for brain death studies.
  • Uses radiopharmaceuticals that are perfusion
    agents
  • 99mTc-DTPA (diethylenetriaminepenta acetic acid)
  • 99mTc-Pertechnetate.
  • 99mTc-DTPA and 99mTc-Pertechnetate do not cross
    an intact blood-brain barrier.

5
Planar Brain Imaging
  • Generally consists of two phases
  • Dynamic or angiographic phase (regional brain
    perfusion).
  • Delayed static images (distribution of
    radiopharmaceutical in the sagittal sinus and
    cerebral regions).

6
Planar Brain Imaging Dynamic Phase Technique
  • 15 to 20 mCi (555 to 740 MBq) of 99mTc-DTPA
    or 99mTc-Pertechnetate is intravenously injected.
  • Planar imaging is immediately obtained.

7
Normal Anterior Radionuclide Angiogram
  • Images demonstrate prompt symmetric perfusion
    that in the anterior projection looks like a
    trident.
  • The middle and cerebral arteries are seen to the
    right and left and the anterior cerebral arteries
    are seen as a single midline vertical line of
    activity.

8
Normal Anterior Radionuclide Angiogram
(99mTc-DTPA)
9
Normal Planar Static Brain Scan
  • On static images, radioactivity does not normally
    lie within the brain itself because of the
    integrity of the blood-brain barrier.
  • Activity is located in the overlying scalp
    tissues, calvarium and subarachnoid space as well
    as within the sagittal and transverse sinuses.

10
Normal Planar Static Brain Scan
11
Anterior Radionuclide AngiogramBrain Death
  • Radionuclide angiogram is a simple, noninvasive
    method of determining the presence or absence of
    intracerebral perfusion and thereby of confirming
    a clinical diagnosis of brain death.
  • 99mTc-Pertechnetate and 99mTc-DTPA are the most
    widely used for this purpose.
  • 99mTc-HMPAO and 99mTc-ECD also can be used.

12
Anterior Radionuclide AngiogramBrain Death
  • Need to see distinct activity in the common
    carotid artery to be assure that the radionuclide
    has been delivered especially when using
    99mTc-HMPAO (99mTc-HMPAO is unstable, inject
    within 30 minutes of preparation).

13
Anterior Radionuclide AngiogramBrain Death
  • In the presence of cerebral death, the injected
    activity typically proceeds through the carotid
    artery to the base of the skull and stops, owing
    to increased intracranial pressure.
  • To prevent mistaking scalp perfusion for
    intracerebral blood flow, an elastic band can be
    placed around the head just above the orbits
    (diminished flow to superficial scalp vessels).

14
Anterior Radionuclide AngiogramBrain Death
15
Brain Death Hot Nose Sign
  • When intracranial carotid blood flow ceases in
    the setting of brain death, increased flow
    through the maxillary branch of the external
    carotid artery may produce markedly increased
    perfusion projecting over the nasal area.

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17
Delayed 99mTc-DTPA ImageBrain Death
  • A single anterior or lateral view is obtained
    within 10 to 15 minutes of the completion of the
    angiographic portion of the study to determine
    the presence of sagittal sinus activity.

18
Delayed 99mTc-DTPA ImageBrain Death
19
Brain Death
  • An actual diagnosis of brain death should not be
    made by using nuclear imaging techniques alone.

20
Cerebrovascular System
  • Radionuclide Brain Imaging
  • Planar Brain Imaging
  • SPECT Brain Perfusion Imaging

21
SPECT Brain Perfusion Imaging
  • Uses lipophilic radiopharmaceuticals that cross
    the intact blood-brain barrier and are retained
    by the brain tissue.
  • Retention of the radiopharmaceutical is
    proportional to regional blood flow (rCBF).

22
SPECT Brain Perfusion Imaging
  • 99mTc-HMPAO
  • hexmethylpropyleneamine oxime
  • Exametazime
  • 99mTc-ECD
  • ethylene L-cysteinate dimer
  • Bicisate

23
SPECT Brain Imaging Technique
  • Inject 10 to 20 mCi (370 to 740 MBq) of
    99mTc-HMPAO or 99mTc-ECD.
  • Limit external external sensory stimuli.
  • Obtain SPECT Images 15 to 20 minutes after
    injection.

24
SPECT Brain Scan Normal Findings
  • Activity is symmetric and greatest in the strip
    of cortex along the convexity of the frontal,
    parietal, temporal and occipital lobes.
  • Activity is also high in regions corresponding to
    subcortical gray matter, including the basal
    ganglia and thalmus.
  • This is consistent with the four-fold greater
    blood flow in the gray matter than in the white
    matter.

25
Normal SPECT Brain Perfusion
26
Normal SPECT Brain Perfusion
27
SPECT Brain Perfusion Imaging Clinical
Applications
  • Suspected brain death.
  • Acute stroke.
  • Transient ischemic attacks.
  • Differentiation of recurrent tumor from radiation
    necrosis.
  • Epilepsy.
  • Dementias, especially Alzheimers.

28
SPECT Brain Perfusion Imaging Cerebral
Infarction
  • Only 20 of CT scans are positive 8 hours after
    cerebral infarction.
  • Acute infarcts are usually identified on
    nonconstrast MRI within 4 to 6 hours.
  • 90 of SPECT brain perfusion images show deficits
    8 hours after cerebral infarction.

29
SPECT Brain Perfusion Imaging Cerebral
Infarction
  • Sensitivity of CT and SPECT imaging are the same
    at 72 hours postinfarction.
  • Small infarcts , particularly those in the white
    matter (lacunar infarcts), may not be detected by
    SPECT.
  • SPECT and PET imaging cannot distinguish between
    hemorrhagic and ischemic infarction.

30
SPECT Brain Perfusion Imaging Cerebral
Infarction
  • During the acute phase of stroke (first hours to
    2 to 3 days after vascular insult) a reduction in
    blood flow to the affected brain is identified.
  • The area of affected brain is often greater on
    SPECT imaging than that seen with CT imaging,
    suggesting tissue at risk (prenumbra) surrounding
    the infarct.

31
Acute and Chronic Infarction
32
SPECT Brain Perfusion Imaging Cerebral
Infarction
  • During the subacute phase of stroke (1 to 3 weeks
    after onset of symptoms), the brain SPECT
    perfusion pattern is complicated by the
    phenomenon of increased perfusion termed,
    luxury perfusion.

33
Infarction with Luxury Perfusion
T1 with Gadolinium
34
SPECT Brain Perfusion Imaging Clinical
Applications
  • Suspected brain death.
  • Acute stroke.
  • Transient ischemic attacks.
  • Differentiation of recurrent tumor from radiation
    necrosis.
  • Epilepsy.
  • Dementias, especially Alzheimers.

35
SPECT Brain Perfusion Imaging Recurrent Brain
Tumor
  • In conjunction with Thallium-201 SPECT brain
    perfusion imaging may be valuable in
    distinguishing between radiation necrosis and
    tumor recurrence.
  • 99mTc-HMPAO generally shows a focal deficit in
    the either necrotic tissue or recurrent tumor.
  • Thallium-201 is a marker of viability localizing
    to living tumor cells but not nonviable tumor
    cells or necrotic tissue.

36
Recurrent Brain Tumor
37
SPECT Brain Perfusion Imaging Epilepsy
  • Patients with partial (focal) epilepsy
    refractory to therapy may benefit from surgical
    ablation of the seizure focus.
  • The most common pathology at the foci is mesial
    temporal scelrosis (gliotic temporal scarring).
  • Although most complex partial seizures arise from
    epilectic foci in the temporal lobes, they may
    arise from other cortical areas.

38
SPECT Brain Perfusion Imaging Epilepsy
  • If seizure foci can be localized to the temporal
    lobes, about 70 of patients undergoing partial
    temporal lobectomy experience amelioration or
    eradication of seizures. .

39
SPECT Brain Perfusion Imaging Epilepsy
  • SPECT and PET imaging attempts to localize
    seizure foci based on the metabolic and perfusion
    status of the seizure focus.
  • Seizure foci may exhibit hyperperfusion and
    hypermetabolism during seizures.
  • 99mTc-HMPAO or ECD for perfusion.
  • 18FDG for evaluating metabolism.

40
Ictal SPECT Brain Imaging 99mTc-HMPAO
41
Ictal 18FDG PET Scan
42
Interictal 18FDG PET Scan
43
SPECT Brain Perfusion Imaging Epilepsy
  • In general, ictal studies are more sensitive in
    the detection of temporal lobe seizure foci than
    are interictal studies, with a sensitivity of 85
    to 95 ictally and about 70 interictally.

44
SPECT Brain Perfusion Imaging Alheimers Disease
  • Most common and highly suggestive finding of
    Alzheimers disease on 99mTc-HMPAO or 99mTc-ECD
    SPECT imaging is symmetric and bilateral
    posterior temporal and parietal perfusion
    defects.
  • Positive predictive value of more than 80.
  • This imaging appearance however is not
    pathognomonic (vascular dementia, Parkinsons
    disease and various encephalopathies).

45
SPECT Brain Perfusion Imaging Alheimers Disease
  • The negative predictive value of of a normal
    SPECT perfusion scan is generally high, and other
    causes for dementia should be sought.
  • PET studies demonstrate hypometabolism patterns
    similar to those seen with SPECT brain perfusion
    agents.

46
SPECT Brain Perfusion Imaging Alheimers
Disease
47
SPECT Brain Perfusion Imaging Alheimers Disease
48
PET Scan Alheimers Disease
49
Outline
  • Cerebrovascular System
  • Thyroid Imaging and Uptake
  • Gastrointestinal Tract
  • Genitourinary System
  • Conventional Neoplasm Imaging
  • Inflammation and Infection Imaging

50
Thyroid Imaging and Uptake
  • Both 123I and 131I are used for iodine uptake.
  • Iodine (123I) and technetium (99mTc) constitute
    the radionuclides used in imaging the thyroid
    gland.
  • Only 131I is used for thyroid therapy.

51
Thyroid Uptake Iodine-131
  • Decays by beta emission and has a half-life of
    8.04 days.
  • High radiation dose to the thyroid.
  • The principle gamma emission of 364 keV is
    considerably higher than the ideal for imaging
    with gamma cameras.
  • Low price.
  • Readily available.

52
Thyroid Imaging and Uptake Iodine-123
  • Decays by electron capture with a photon energy
    of 159 keV.
  • Half life of 13 hours.
  • Lower radiation dose to the thyroid.
  • High cost because it is produce by cyclotron.
  • Iodine of choice for thyroid imaging.

53
Thyroid Imaging Technetium-99m
  • Technetium-99m pertechnetate is trapped by the
    thyroid in the same manner as iodides but is not
    organified.
  • 6 hour half-life.
  • Principle gamma energy of 140 keV.
  • Readily available.
  • Only 1 to 5 of administered activity is trapped
    by the thyroid, so image background is high.

54
Iodine Uptake Test
  • Thyroid uptake is based on the principle that the
    administered radiopharmaceutical is concentrated
    by the thyroid gland in a manner that reflects
    the glands handling of stable dietary iodine and
    therefore the functional status of the gland.

55
Iodine Uptake Test
  • The diagnosis of hyperthyroidism or
    hypothyroidism is not made by using radioactive
    iodine.
  • Serum measurements of thyroid hormone or
    thyroid-stimulating hormone (TSH) are used to
    diagnose hyperthyroidism or hypothyroidism.

56
Iodine Uptake Test Technique
  • Uptake is conventionally expressed in as the
    percentage of the administered activity in the
    thyroid gland at a given time after
    administration.

57
Iodine Uptake Test Technique
  • 5 ?Ci (0.2 MBq) of 131I-sodium or 10 to 20 ?Ci
    (0.4 to 0.7 MBq) of 123I-sodium administered in
    capsule or liquid form.
  • An identical amount of activity, standard, is
    placed in a neck phantom and compared with that
    in the patients thyroid using a single-crystal
    counting probe with a flat-field collimater.

58
Iodine Uptake TestNormal Results
  • 4-hour 6 to 18
  • 24 hour 10 to 30

59
Iodine Uptake Test Results
  • 4-hour 6 to 18
  • 24 hour 10 to 30
  • Glands demonstrating a poor avidity for iodide
    are considered to be hypofunctioning.
  • Glands demonstrating increased avidity for iodide
    are considered to be hyperfunctioning.

60
Elevated Radioiodine Uptake
  • Primary hyperthyroidism (Graves disease or toxic
    nodular goiter) and secondary hyperthyroidism
    (increased production of TSH by the pituitary)
    commonly produce elevated iodine uptakes.
  • Toxic nodular goiters (Plummers disease) may
    yield uptake values in the high, normal or mildly
    elevated range.

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62
Reduced Radioiodine Uptake
  • Primary or secondary hypothyroidism may produce
    decreased radioiodine uptake however because of
    the prevalence of iodine in the American diet it
    has become increasingly difficult to use reduced
    radioiodine uptake as in indicator of
    hypothyroidism.

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65
Thyroid Imaging and Uptake
  • Both 123I and 131I are used for iodine uptake.
  • Iodine (123I) and technetium (99mTc) constitute
    the radionuclides used in imaging the thyroid
    gland.
  • Only 131I is used for thyroid therapy.

66
Thyroid Gland Imaging Indications
  • To relate the general structure of the gland to
    function, particularly in differentiating Graves
    disease from toxic multinodular goiter.
  • To determine function in a specific area (ie to
    see if a palpable nodule is functional).
  • To locate ectopic tissue.
  • To assist in the evaluation of congenital
    hypothyroidism or organification defects.
  • To determine if a cervical or mediastinal mass is
    thyroid tissue.

67
Thyroid Imaging Technique
  • Image the thyroid gland 20 minutes after the
    intravenous administration of 5 to 10 mCi (185 to
    370 MBq) of 99mTc-Pertechnetate using a
    scintillation camera with a pinhole collimater.
  • Imaging with 123I is performed 16 to 24 hours
    after the oral administration of 200 to 600 ?Ci
    (7.4 to 22.2 MBq) to a fasting patient.

68
Normal Iodine-123 Thyroid Scan
69
99mTc-Pertechnetate Thyroid Scan Lingual Thyroid
70
123I or 131I imaging of the ChestSubsternal
thyroid
71
99mTc-Pertechnetate Thyroid ScanCongenital
Organification Defect
72
Thyroid Nodules
  • Fine-needle aspiration biopsy has largely
    supplanted radionuclide imaging as the initial
    investigative procedure for palpable thyroid
    nodules.
  • Thyroid imaging can be useful in patients with
    indeterminate cytology results or with suppressed
    TSH levels.

73
Thyroid Nodules
  • Nodules are classified at imaging with respect to
    the relative amount of activity present.
  • Cold nodules demonstrate absence of activity.
  • Hot nodules demonstrate focally increased
    activity.

74
Cold Nodules
  • Nonspecific finding.
  • Most cold nodules are benign.
  • The small percentage of cold nodules that prove
    to be cancerous are sufficient to warrant further
    investigation of all cold nodules.
  • The reported percentage of cold nodules harboring
    thyroid cancer varies depending on the study but
    is generally thought to be about 20.
  • Likelihood of cancer increases if the patient is
    young.

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77
99mTc-Pertechnetate Thyroid Scan Nonfunctioning
Thyroid Adenoma
78
Hot Nodules
  • Most nodules that demonstrate increased
    radionuclide activity are benign, although
    thyroid carcinoma has been describe in a small
    percentage (lt1).
  • Hot nodules almost always represent
    hyperfunctioning ademonas half of these
    hyperfunctioning adenomas are autonomous (not
    suppressible with exogenous thyroid hormone).
  • Autonoumous hyperfunctioning nodule may produce
    enough thyroid hormone to inhibit pituitary
    secretion of TSH.

79
99mTc-Pertechnetate Thyroid Scan
80
Discordant Thyroid Nodule
  • A small number of cases of hot nodules on
    99mTc-Pertechnetate imaging have subsequently
    proved to be cold or discordant on iodine
    imaging.
  • A small number of these discordant lesions have
    been shown to be thyroid carcinoma.
  • Discordant images are believed to be produced by
    either lack of organification of iodine or the
    rapid turnover of organified iodine.

81
Discordant Thyroid Nodule
  • Keep in mind that 99mTc-Pertechnetate imaging
    occurs 20 minutes after injection while
    radioiodine imaging is normally performed 24
    hours after ingestion of the radiopharmaceutical.
  • It has been recommended that patient with hot
    nodules on pertechnetate scan be re-imaged using
    an iodine agent to determine whether a lesion
    represents a discordant nodule (further
    workup/biopsy) or a true hyperfunctioning adenoma.

82
Discordant Thyroid Nodule
Mixed papillary follicular carcinoma
83
99mTc-Pertechnetate Thyroid Scan
84
Diffuse Toxic Goiter (Graves Disease)
  • Thought to be of autoimmune origin.
  • Presents with thyromegaly.
  • On 99mTc-Pertechnetate scan, the thyroid has
    uniform increased activity and the salivary
    glands are difficult to identify.
  • Because salivary glands are not normally seen on
    123I scan, it is often difficult to differentiate
    Gravess disease from a normal scan.
  • 24-hour iodine uptake is high, in the range of
    40 to 70.

85
99mTc-Pertechnetate Thyroid Scan
86
Diffuse Goiter in Patient with Graves
87
Acute and Subacute Thyroiditis
  • Acute (bacterial) and subacute (viral or
    autoimmune) thyroiditis are uncommon diseases and
    have such typical clinical feature that they are
    usually diagnosed on physical and clinical
    grounds alone.
  • Subacute thyroiditis usually presents as a
    painful swollen gland with elevated circulating
    thyroid hormone levels but markedly decreased
    radioiodine uptake.

88
99mTc-Pertechnetate Thyroid Scan
89
Chronic Thyroiditis
  • Chronic thyroiditis (Hashimotos thyroiditis) is
    the most common form of inflammatory disease of
    the thyroid.
  • Thought to be autoimmune in origin.
  • More common in females.
  • Thyromegaly is usually the presenting symptom.
  • Depending on the stage and severity, symptoms of
    mild hyper- or hypo-thyroidism may be present.

90
Chronic Thyroiditis
  • Scan appearance varies from diffusely uniform
    increased activity in the gland early in the
    disease (which may resemble Graves disease) to a
    coarsely patchy distribution of activity within
    the gland later in the disease (which may mimic
    multinodular goiter).

91
123I Thyroid Scan Chronic Thyroiditis
92
Multinodular Goiter
  • Typically presents as an enlarged gland with
    multiple cold, warm and hot areas.
  • Nodule generally constitute a spectrum of thyroid
    adenomas ranging from hyperfunctioning to cytic
    or degenerative lesions.
  • Most commonly seen in middle aged women.
  • In adults, the cold lesions identified in
    multinodular goiter are significantly less likely
    to represent carcinoma than a solitary cold
    nodule.

93
99mTc-Pertechnetate Thyroid ScanMultinodular
Goiter
94
Thyroid Carcinoma
  • 90 of all thyroid cancers are well-differentiated
    .
  • 80 to 90 are papillary thyroid cancers.
  • 10 to 20 are follicular thyroid cancers.
  • Metastatic disease from well-differentiated
    thyroid cancers have the ability to concentrate
    iodine thus making them amenable to metastasis
    localization and adjunctive radioiodine therapy.
  • Overall prognosis of patients with
    well-differentiated types of thyroid cancer is
    good (95 5-year survival).

95
Thyroid Carcinoma
  • Papillary thyroid carcinoma frequently
    metastasizes to the cervical lymph nodes.
  • Follicular thyroid carcinoma frequently
    metastasizes hematogenously to the lungs and
    bones (65 to 85 concentrate radioiodine).

96
Whole-body 131I Scan Follicular Thyroid Cancer
Metastatic Disease
97
Thyroid Carcinoma
  • 5 of thyroid carcinoma is anaplastic or poorly
    differentiated.
  • Occur primarily in older patients.
  • Poor prognosis.
  • Medullary carcinoma of the thyroid constitutes 5
    of malignant thyroid lesions.
  • Hurthle cell carcinoma is a variant of follicular
    cell carcinoma, is generally more aggressive and
    metastasizes early.
  • Metastasis from above types of tumors do not
    concentrate iodine well.

98
Thyroid Carcinoma
  • Non-radioiodine-avid thyroid carcinomas can be
    successfully imaged using either 99mTc-sestamibi
    or fluorine-18 deoxyglucose (18FDG) positron
    emission tomography.

99
99mTc-Sestamibi scan
100
18FDG PETscan Thyroid Cancer
101
Thyroid Carcinoma
  • Whole-body evaluation for metastatic thyroid
    disease (well-differentiated) is first performed
    within 1 to 2 months after total or subtotal
    thyroidectomy.
  • Thyroid hormone is withheld during this period to
    all for endogenous TSH stimulation of any
    remaining normal tissue in the thyroid bed and
    any functioning metastatic lesions.

102
Thyroid Carcinoma
  • 3 to 5 mCi (111 to 185 MBq) of 131I is
    administered orally and sequential whole-body
    images are obtained over the next 48 hours.
  • Knowledge of the whole-body distribution of
    radioiodine before and after ablation is
    essential.
  • 131I activity is commonly seen in the salivary
    glands, stomach, bowel and bladder.
  • Mild diffuse activity in the liver is also normal
    and caused by clearance of the bound iodine by
    the liver.

103
Whole-body 131I Scan Pre- and Post-Ablation or
Total Thyroidectomy
104
Thyroid Carcinoma
  • Metastatic lesions are only infrequently
    visualized with 123I or 131I whole-body imaging
    when there is functioning thyroid tissue in the
    neck.
  • Ablation of residual tissue allows for sufficient
    TSH stimulation of distant metastatic sites, thus
    allowing for their detection on follow-up
    imaging.
  • Once all the residual thyroid tissue in the neck
    has been ablated, follow-up imaging with 123I or
    131I may be performed at 6-month to 1-year
    intervals.

105
Whole-body 131I Scan Residual Thyroid Tissue
and Star Artifact
106
Metastatic Thyroid Cancer
107
Outline
  • Cerebrovascular System
  • Thyroid Imaging and Uptake
  • Gastrointestinal Tract
  • Genitourinary System
  • Conventional Neoplasm Imaging
  • Inflammation and Infection Imaging

108
Gastrointestinal Tract
  • Liver-Spleen Imaging.
  • Hepatic Blood Pool Imaging.
  • Gastrointestinal Bleeding Studies.
  • Hepatobiliary Imaging.

109
Liver-Spleen Imaging Indications
  • Confirmation or evaluation of suspected
    hepatocellular diseases, hepatomegaly or
    splenomegaly.
  • Confirmation of specific space-occupying lesions
    such as focal nodular hyperplasia.

110
Liver-Spleen Imaging Radiopharmaceuticals
  • Radionuclide imaging of the liver and spleen
    capitalizes on a function common to both of these
    organs phagocytosis.
  • 99mTc-sulfur colloid.
  • Average particle size of 0.3 to 1.0 ?m.
  • Reticuloendothelial system (Kupffer cells) .
  • 80 to 90 of injected particles are sequestered
    by the liver.
  • 5 to 10 localize in the spleen.

111
Liver-Spleen Imaging Technique
  • Both planar and SPECT imaging techniques are
    used.
  • 4 to 6 mCi (148 to 222 MBq) of 99mTc-sulfur
    colloid.
  • Image 5 to 10 minutes after injection to allow
    for adequate accumulation in the liver.
  • Anterior, posterior and oblique views are often
    obtained.
  • A marker is often placed at right inferior costal
    margin for localization.

112
Normal sulfur colloid liver-spleen scan
113
Liver-Spleen Imaging
  • Any localized space-occupying process in the
    liver may present as a focal area of decreased
    activity.
  • Lesions as small as 8 mm may be identified.
  • Lesions 2 to 2.5 cm are routinely imaged.
  • Defects in the hepatic parenchyma are
    nonspecific.
  • Solitary intrahepatic defects may be produced by
    various lesions.

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115
Liver-Spleen Imaging
  • In any patient with several liver defects,
    metastatic disease must be a primary
    consideration.

116
Metastatic Colon Carcinoma
117
Liver-Spleen Imaging Colloid Shift
  • Increased radiocolloid concentration by the
    spleen and bone marrow compared with the liver is
    called colloid shift.
  • Found in patients with diseases that cause
    derangement of hepatic function and/or portal
    hypertension.
  • Hepatic cirrhosis is the most common abnormality
    presenting in this fashion.

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119
Cirrhosis with Ascites
120
Hepatitis
121
Liver-Spleen Imaging Primary Liver Neoplasms
  • Hepatoma.
  • Focal nodular hyperplasia.
  • Hepatic cell adenoma.

122
Liver-Spleen Imaging Primary Liver Neoplasms
  • Hepatoma.
  • Focal defect on sulfur colloid imaging
  • Multifocal forms exist.
  • Frequently occur in association with preexisting
    hepatic disease, most notably alcoholic
    cirrhosis.
  • Hepatomas are also generally gallium-67 avid.
  • Focal nodular hyperplasia.
  • Hepatic cell adenoma.

123
Hepatoma in a Patient with Cirrhosis
124
Liver-Spleen Imaging Primary Liver Neoplasms
  • Hepatoma.
  • Focal nodular hyperplasia.
  • Asymptomatic mass.
  • Contain Kupffer cells (normally concentrate and
    occasionally hyperconcentrate radiocolloid).
  • In most cases they appear indistinguishable from
    normal hepatic parenchyma on sulfur collid scan.
  • Hepatic cell adenoma.

125
Focal Nodular Hyperplasia
126
Liver-Spleen Imaging Primary Liver Neoplasms
  • Hepatoma.
  • Focal nodular hyperplasia.
  • Hepatic cell adenoma.
  • Usually encounter in young women who have used
    birth control pills.
  • Ususally asymtomatic but can hemorrhage.
  • Kupffer cell are not a prominent feature of these
    lesions.
  • Present a focal defects on colloid imaging.

127
Gastrointestinal Tract
  • Liver-Spleen Imaging.
  • Hepatic Blood Pool Imaging.
  • Gastrointestinal Bleeding Studies.
  • Hepatobiliary Imaging.

128
Hepatic Blood Pool Imaging
  • Confirmation that an asymptomatic lesion seen on
    either ultrasound or contrast enhanced CT
    examination is a cavernous hemangioma.
  • Cavernous hemangioma is highly likely when a
    defect seen with 99mTc-sulfur colloid imaging
    shows increased activity after administration of
    a 99mTc-labeled blood pool agent, such as
    99mTc-red blood cells.
  • Use of SPECT imaging increases the sensitivity.

129
99mTc-Red Blood Cell Scan Hepatic Hemangioma
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131
Gastrointestinal Tract
  • Liver-Spleen Imaging.
  • Hepatic Blood Pool Imaging.
  • Gastrointestinal Bleeding Studies.
  • Hepatobiliary Imaging.

132
Gastrointestinal Bleeding Studies
  • Both 99mTc- red blood cells and 99mTc sulfur
    colloid can effectively be used to localize
    gastrointestinal bleeding.
  • Red blood cells are almost always used and have
    greater specificity.
  • Because of significant background activity in the
    upper abdomen and the diagnostic efficacy of EGD,
    nuclear medicine imaging are most advantageous in
    evaluating lower GI bleeding.

133
Gastrointestinal Bleeding Studies
  • Common causes of lower GI bleeding in adults are
  • Diverticular disease.
  • Angiodysplasia.
  • Neoplasms.
  • Inflammatory bowel disease.
  • Bleeding rates on the order of 0.2 mL/minute are
    reliable detected with radionuclide techniques.

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99mTc-Red Blood Cells Proximal Small Bowel
Bleeding
136
99mTc-Red Blood Cells Lower Gastrointestinal
Bleeding
137
Gastrointestinal Tract
  • Liver-Spleen Imaging.
  • Hepatic Blood Pool Imaging.
  • Gastrointestinal Bleeding Studies.
  • Hepatobiliary Imaging.

138
Hepatobiliary Imaging
  • Accurate and convenient imaging in acute and
    chronic biliary states.
  • Common indications
  • Acute (calculous or acalculous) cholecystitis.
  • Biliary patency.
  • Identification of biliary leaks.
  • Differentiation of biliary atresia from neonatal
    hepatitis in neonates.

139
Hepatobiliary Imaging Radiopharmaceuticals
  • Analogs of 99mTc-iminodiacetic acid (IDA).
  • Most widely used is diisopropyl IDA (DISIDA
    disofenin or Hepatolite).
  • Rapidly removed from the the circulation by
    active transport into the hepatocytes and
    secreted into the bile canaliculi, then the
    biliary radicals, bile duct, gallbladder and
    small intestine.
  • IDA analogs are excreted without being
    conjugated.

140
Hepatobiliary Imaging Technique
  • In patients with acute disease, a minimum of 2
    hours of fasting is suggested.
  • 3 to 10 mCi (111 to 370 MBq) of 99mTc-labeled IDA
    in injected intravenously.
  • Anterior planar images are obtained at 5-minute
    intervals for the 1st half-hour of the study.
  • Similar images are then obtained at 10 minute
    intervals.

141
Hepatobiliary Imaging Interpretation
  • Normally the gallbladder is visualized in the
    first half-hour of the study, as are the common
    bile duct and duodenum.
  • Visualization of the gallbladder confirms that
    the cystic duct is patent.
  • If the above structures are not identified at 1
    hour, delayed images should be obtained for up to
    4 hours.

142
Normal 99mTc-DISIA Hepatobiliary Scan
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Acute Cholecystitis
  • More than 95 of patients with acute
    cholecystitis have cystic duct obstruction.
  • In the proper clinical setting, the diagnosis of
    acute cholecystitis (calculus or acalculus) in a
    fasting patient may be reliably made in the
    presence of normal hepatic uptake and excretion
    of the radiopharmaceutical through the common
    duct, but without visualization of the
    gallbladder over a period of 4 hours after
    injection.

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Technetium-99m Hepatobiliary ScanAcute
Cholecystitis
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Rim Sign of Acute Cholecystitis
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Rim Sign of Acute Cholecystitis
  • Also called the pericholecystic hepatic activity
    sign.
  • Seen in about 20 of patients whose gallbladders
    are not visualized on hepatobiliary scans.
  • May be the result of inflammation causing
    regional hepatic hyperemia.
  • 40 of patients with a rim sign have either a
    perforated or a gangrenous gallbladder.

148
Rim Sign of Acute Cholecystitis
149
Cystic Duct Sign
  • Small nubbin of activity in the cystic duct
    proximal to the site of obstruction.

150
Cystic Duct Sign
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Use of Pharmacologic Intervention
  • Morphine causes constriction of the sphincter of
    Oddi (increased smooth muscle tone) with
    subsequent rise in intraductal pressure in the
    common duct by 60, producing increased flow of
    the radiopharmaceutical into the gallbladder.
  • Typical dosage is 0.04 mg/kg diluted in 10 mL of
    saline.
  • Nonvisualization of the gallbladder 30 minutes
    after morphine has the same implication as lack
    of visualization on 4-hour images.

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Morphine Augmentation
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Normal Gallbladder Response to Cholecystokinin
(CCK)
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Abnormal Gallbladder Response to Cholecystokinin
(CCK)
156
Hepatobiliary Imaging
  • Accurate and convenient imaging in acute and
    chronic biliary states.
  • Common indications
  • Acute (calculous or acalculous) cholecystitis.
  • Biliary patency.
  • Identification of biliary leaks.
  • Differentiation of biliary atresia from neonatal
    hepatitis in neonates.

157
Technetium-99m Hepatobiliary ScanBiliary Leak
158
Hepatobiliary Imaging
  • Accurate and convenient imaging in acute and
    chronic biliary states.
  • Common indications
  • Acute (calculous or acalculous) cholecystitis.
  • Biliary patency.
  • Identification of biliary leaks.
  • Differentiation of biliary atresia from neonatal
    hepatitis in neonates.

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Biliary Atresia and Neonatal Hepatitis
  • Imaging with 99mTc-IDA analogs has been used to
    exclude a diagnosis of biliary atresia by
    demonstrating patent extrahepatic biliary systems
    in jaundiced neonates.
  • In the absence of visualization of the biliary
    tree, atresia may not be successfully
    differentiated from severe hepatocellular disease
    produced by neonatal hepatitis.
  • Phenobarbital stimulated excretion of
    radiopharmaceutical.

160
Technetium-99m Hepatobiliary ScanNeonatal
Hepatitis
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Technetium-99m Hepatobiliary ScanBiliary Atresia
162
Gastrointestinal Tract
  • Liver-Spleen Imaging.
  • Hepatic Blood Pool Imaging.
  • Gastrointestinal Bleeding Studies.
  • Hepatobiliary Imaging.

163
Outline
  • Cerebrovascular System
  • Thyroid Imaging and Uptake
  • Gastrointestinal Tract
  • Genitourinary System
  • Conventional Neoplasm Imaging
  • Inflammation and Infection Imaging

164
Genitourinary Imaging
  • With the widespread use of computed tomography
    and ultrasound, the evaluation of renal anatomy
    by nuclear techniques has diminished.
  • The role of nuclear renal scanning has become
    confined to functional analysis.

165
Radionuclide Renal Evaluation
  • Anatomic imaging (visual assessment of renal
    cortex).
  • Renal functional imaging visual assessment of
    renal blood flow, uptake and excretion.
  • Renogram time-activity curve that provides a
    graphic representation of the uptake and
    excretion of a radiopharmaceutical by the
    kidneys.

166
Anatomic (Cortical) Imaging
  • Usually performed for evaluation of
  • Space-occupying lesions.
  • Functioning pseudotumors such as cortical columns
    of Bertin.
  • Edema or scarring associated with acute or
    chronic pyelonephritis, especially in children.
  • 99mTC-DSMA (dimercaptosuccinic acid) and SPECT
    are generally used.

167
99mTc-DMSA Cortical Imaging of the Kidneys
168
99mTc-DMSA Pyelonephritis
169
Radionuclide Renal Evaluation
  • Anatomic imaging (visual assessment of renal
    cortex).
  • Renal functional imaging visual assessment of
    renal blood flow, uptake and excretion.
  • Renogram time-activity curve that provides a
    graphic representation of the uptake and
    excretion of a radiopharmaceutical by the
    kidneys.

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Renal Physiology
  • The excretory function of the kidneys consists of
    two primary mechanisms
  • Passive filtration through the glomerulus.
  • Active secretion by the tubules.

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Genitourinary Imaging Radiopharmaceuticals
  • Those excreted by tubular secretions.
  • 99mTc-MAG3.
  • Those excreted by glomerular function.
  • 99mTc-DTPA.
  • Those bound in the renal tubules for a
    sufficiently long time to permit cortical
    anatomic imaging.
  • 99mTc-dimercaptosuccinic acid (DMSA).

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Functional Renal Imaging
  • Alternative to intravenous urography providing
    anatomic, functional and collecting system
    patency information.
  • Has two phases
  • Renal perfusion (renal blood flow)
  • Renal function

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Functional Renal Imaging Technique
  • Intravenous injection of 10 to 20 mCi (370 to 740
    MBq) of 99mTc-DTPA (glomerular) or 99mTc-MAG3
    (tubular).
  • Imaging renal perfusion is usually begun as the
    bolus is visualized in the proximal abdominal
    aorta with subsequent serial images made every 1
    to 5 seconds.

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99mTc-DTPA Normal renal blood flow
175
Functional Imaging Technique
  • At the end of the renal perfusion sequence,
    imaging for renal function begins.
  • Dynamic or sequential static, 3 to 5 minute
    images are obtained over 20 to 30 minutes.

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99mTc-MAG3 Normal Renogram
177
Functional Renal Imaging Technique
  • Time-activity curves (renograms) are created from
    regions of interest placed over the renal
    parenchyma on the sequential static images.
  • Renograms are graphic representations of the
    uptake and excretion of a radiopharmaceutical.
  • The classic renogram curve is obtained using
    agents that are eliminated by tubular secretion.
    (e.g. ,99mTc-MAG3).

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Typical Regions of Interest for Computer Analysis
179
Typical Renogram Curve
180
Renography
  • The normal-computer generated renogram curve
    using a tubular radiopharmaceutical consists of
    three phases
  • Renal perfusion or vascular transit phase (30 to
    60 seconds).
  • Cortical or tubular concentration phase (1 to 5
    minutes).
  • Clearance or excretion phase.

181
Typical Renogram Curve
182
Renography
  • The renogram curves for each kidney should be
    relatively symmetric.
  • The shapes of the curves should be inspected for
    alterations from the normal configuration.

183
Renography
  • Data commonly derived from 99mTc-MAG3 renograms
    include
  • Time to peak activity Normal is 3 to 5 minutes.
  • Relative renal uptake ratios at 2 to 3 minutes
    Activity of each kidney should be equal, ideally
    50. A value of 40 or less is considered
    abnormal.
  • Half-time excretion Time for half of the peak
    activity to be cleared. Normal is 8 to 12
    minutes.

184
99mTc-MAG3 Acute Pyelonephritis
185
99mTc-MAG3 Acute Pyelonephritis
186
Posterior Flow Images after 99mTc-MAG3Acute
Tubular Necrosis
187
Typical Renogram Curve
188
Posterior Flow Images after 99mTc-MAG3Acute
Tubular Necrosis
189
Posterior Flow Images after 99mTc-MAG3Acute
Tubular Necrosis
190
Diuretic Renography
  • In patients with nonobstructive hydronephrosis
    and/or hydroureter due to vesicoureter reflux,
    previous obstruction or functional uretopelvic
    disorders, the dilated intrarenal collecting
    system may fill but not reach pressures
    sufficient to open the ureteropelvic junction.
  • This give the impression of a fixed anatomic
    abnormality rather than a functional abnormality.

191
Diuretic Renography
  • By increasing urine flow using a diuretic
    (Lasix), a functional obstruction may be overcome
    by increasing pressure in the renal pelvis and
    thus allowing urine to flow from the collecting
    system into the ureter and bladder.
  • Differentiation of a fixed anatomic from a
    functional abnormality.

192
Characterisitic Time-activity Curves in a
Diuretic Renogram
193
Non-obstructed Patulous Collecting System
194
Non-obstructed Patulous Collecting System
195
Abnormal Diuretic Renogram with Obstruction
196
Abnormal Diuretic Renogram with Obstruction
197
High Grade Obstruction of the Right Kidney
Collecting System
198
Captopril Renography
  • Renovascular (renal artery stenosis) hypertension
    constitutes about 1 to 4 of all cases of
    hypertension.
  • Most common cause of renal artery stenosis is
    atherosclerosis, predominantly in the elderly
  • The second most common cause is fibromuscular
    dysplasia, occurring primarily in women younger
    than 35 years.

199
Renal Artery Stenosis
  • Significant renal artery stenosis (60 to 75)
    decreases afferent arteriolar blood pressure
    which stimulates renin secretion by the
    juxtaglomerular apparatus.
  • Renin secretion ultimately results in the
    formation of Angiotensin II which vasoconstricts
    efferent arterioles.
  • Effferent arteriolar constriction restores
    glomerular filtration pressure and rate (GFR).

200
Captopril Renography
  • When an ACE inhibitor is given to a patient with
    renal artery stenosis, there is a decrease in GFR
    that is scintigraphically detectable.
  • Captopril renography is highly specific for renal
    artery stenosis.
  • A positive test indicates that the patients
    hypertension is renin dependent, most commonly
    produced by renal artery stenosis, and that it is
    likely to be improved by renal revascularization.

201
Renal Artery Stenosis
  • Patients should be selected carefully and limited
    to those with a moderate to high probability of
    renovascular hypertension.

202
Renal Artery Stenosis
  • Selection criteria includes
  • Initial presentation of hypertension older than
    60 years or younger than 20 years.
  • Severe or accelerated hypertension resistant to
    medication therapy.
  • Hypertension previously well controlled but now
    difficult to manage medically.
  • Hypertension in patients with other evidence of
    vascular disease.
  • Unexplained renal dysfunction in patients with
    recent onset of hypertension.
  • Unexplained hypertension in patients with
    abdominal bruits.

203
Captopril Renography
  • Using the glomerular agent 99mTc-DTPA, the
    principle finding is decreased uptake and
    excretion caused by the captopril induced drop in
    glomerular filtration.
  • Using the primarily tubular agent 99mTc-MAG3, the
    captopril induced drop in GFR results in
    increased cortical retention.

204
Pre- and Post-Captopril 99mTc-MAG3
205
Pre-CaptoprilRenal Blood Flow and Renogram
99mTc-MAG3
206
Post-CaptoprilRenal Blood Flow and Renogram
99mTc-MAG3
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Outline
  • Cerebrovascular System
  • Thyroid Imaging and Uptake
  • Gastrointestinal Tract
  • Genitourinary System
  • Inflammation and Infection Imaging
  • Conventional Neoplasm Imaging

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POST
  • Extra CNS Slides

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POST
  • Extra Thyroid and Parathyroid Slides

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POST
  • Extra GI Slides

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Attenuation Secondary to Breast Tissue
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Accessory Spleen
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Splenic Abscess
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Splenic Infarcts
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Lymphoma of the Spleen
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Long-standing common bile duct obstruction
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Meckels Scan
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Gastric Emptying
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Abnormal Diuretic Renogram with Obstruction
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