Oral Exam - MSK Flashcards

1
Q

Bone scan tips

A
  • Increased uptake between ribs on bonescan is concerning for osteosarcoma lung metastases
  • Heterotopic ossification after surgery can be difficul tto distinguish on bone scan from tumor recurrence
  • Postsurgical change can show increased bone uptake on bone scan
  • New uptake in area of benign lesions could represent fracture or malignant transformation
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2
Q

Malignant Hot lesions ddx:

A

Chondrosarcoma, Ewing sarcoma, osteosarcoma,

metastases, adamantinoma

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3
Q

Malignant cold lesions ddx:

A

Multiple myeloma; metastases - purely lytic

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4
Q

Benign hot lesions ddx:

A

Paget disease, osteoblastoma, chondroblastoma,

aneurysmal bone cyst, osteoid osteoma, giant cell tumor

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5
Q

Iso or mild lesions ddx

A

Fibrous dysplasia, fibrous cortical

defect, nonossifying fibroma, enchondroma

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6
Q

Adamantinoma findings

A

– Anterior tibial cortex

– Low-grade malignant lesion – Focal increased uptake

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7
Q

Osteoid osteoma

A

– Cortically based lesion most commonly in femur, tibia,
spine, hands, and feet
– Double density sign - intense central uptake, & moderate uptake in surrounding area
– Delayed uptake in nidus secondary to presence of
osteoblasts

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8
Q

Fibrous dysplasia

A

– Medullary lesion
– Monostotic: Femur, ribs, tibia, facial bones, & humerus – Polyostotic: Femur, tibia, pelvis, feet, ribs, facial bones,
& lumbar spine

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9
Q

Giant cell tumors

A

– Epiphyseal in location
– Distal femur, proximal tibia, distal radius, sacrum, &
proximal humerus
– Increased tracer uptake peripherally with photopenia
centrally (doughnut sign)

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10
Q

Aneurysmal bone cyst

A

– Eccentrically in medullary cavity
– Posterior elements of spine
– Metaphysisoflongbones
– Upper & lower limbs, spine, & sacrum
– Can show diffuse homogeneous uptake or peripheral
uptake & central photopenia

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11
Q

Enchondroma

A

– Typically solitary lesions in central medullary cavity
– If solitary, more common in hand
– Multiple lesions (Ollier disease & Maffucci syndrome)
– Femur, tibia, humerus, hands, & feet
– Mildly increased uptake in lesions that are large
enough for gamma camera detection
– Fractures can show change in uptake when following
these lesions
– Bone scan cannot reliably differentiate low-grade
chondrosarcoma from enchondroma

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12
Q

Bone island

A

– Medullary in location
– Can occur anywhere, but more often in pelvis, femurs,
and ribs
– Osteopoikilosis: Multiple enostoses near joints &
predominantly in appendicular skeleton
– Most bone islands have no uptake on bone scan;
larger lesions may show very mild uptake

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13
Q

Chondroblastoma

A

– Well-defined,osteolyticlesionwiththinscleroticrim
located in epiphysis or apophyses of long bone
– Femur,tibia,humerus,patella,andtarsalbones
– Skeletallyimmaturepatient
– Bonescanshowsfocalincreaseduptake

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14
Q

Osteochondroma

A

– Most common benign bone tumor
– Most commonly in long bones of upper & lower
extremity: Femur, tibia, humerus
– Uptake on bone scan is directly correlated with degree of enchondral bone formation

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15
Q

Solitary bone lesion

A

○ Only 15% of solitary lesions on bone scan are metastases (spine is most common site)
– Exception: 80%of solitary sternal lesions in breast
cancer patients are metastatic
– Vertebrae: Asymmetric, focal uptake (not confined to
endplate), involvement of pedicle suggestive of
metastasis

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16
Q

Rib metastasis findings

A

○ Solitary rib lesion often benign (~10%metastases)

– Ribs: Long, linear uptake suggestive of metastasis, may be expansile

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17
Q

Ddx photopenic metastases

A

Lytic metastases (RCC, thyroid, myeloma, poorly differentiated anaplastic tumours) +/- lung, breast, NB

Radiation

Bone infarct

AVN

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18
Q

Superscan findings

A

Disseminated bone lesions with diffusely increased skeletal activity, relative absence of renal and soft tissue activity
○ Breast and prostate cancers most common

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19
Q

DDX mets

A

Degenerative changes, arthropathies
Healing fractures
Physiologic activity
Primary bone tumour (benign and malignant)
AVN, osteonecrosis, infarct
Metabolic bone disease, infection/inflammation

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20
Q

Fibrous dysplasia associated abnormalities

A

• Associated abnormalities
○ Calvarial and facial asymmetry, exophthalmos

○ Femur
– Coxavara(shepherd’scrook)

○ McCune-Albright syndrome
– FD
– Café au lait spots
– Endocrinopathy
□ Precociouspuberty 
□ Hyperthyroidism
□ Acromegaly
□ Cushingsyndrome

○ Mazabraud syndrome
– Single or multiple intramuscular myxomas with
fibrous dysplasia; rare

○ Associatedwithaneurysmalbonecysts(ABC)

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21
Q

FD ddx

A

Benign/Malignant bone tumours

Paget’s

Neurofibromatosis

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22
Q

Paget’s findings

A

Intense activity expansile appearance of entire affected bone on bone scan
• Pelvis(30-75%)>vertebra(30-75%)>skull(25-65%)> proximal long bones (esp. femur)
– Typically involves whole bone
– Inactive or quiescent phase should show no increased
uptake
– Osteoporosis circumscripta may show uptake at
margins of lesion

○ Angiographic images from 3-phase bonescan show
increased blood flow with intensity closely correlating
with level of disease activity

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23
Q

Paget’s ddx

A

Mets
Primary bone tumour (radiographs to separate)
Fibrous dysplasia (ribs, skull, femur), spine and pelvis less common than Paget’s

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24
Q

BMD - when to report z score

A

Z-scores are reported for premenopausal women and men under age of 50
○ Z-scoreof-2.0 or lower is belowexpectedrangeforage
○ Z-score above -2.0 is within expected range for age

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25
Q

Prosthetic joint loosening

A
  • Major causes include micromotion over time and osteolysis (e.g., particle disease)
  • 3-phase bone scan: Variable activity on first 2 phases, focal activity at bone-prosthesis site of motion on delay phase

– Activity at tip of prosthesis in cemented hip prosthesis 1 year after placement suggests loosening

– Diffuse periprosthetic uptake of tracer suggests osteolysis from infection or loosening

○ All prosthesis initially show increased activity
– 2-3 years after placement, negative study (periprosthetic activity ≤ surrounding nonarticular bone) has very high negative predictive value

○ Hip arthroplasty
– 10% show increased activity at 2years
- periprosthetic activity in non-cemented arthroplasty 2-3 yrs after placement = loosening
– Activity tip of prosthesis in cemented hip prosthesis 1 year after placement = loosening

○ Knee arthroplasty
– Tibial component > femoral component; increased
activity frequently persists for years

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26
Q

Prosthetic Joint Infection

A
  • Infection rate <1% in primary joint replacement, increased to as high as 15% in revision shoulder arthroplasty
  • Vast majority occur < 90 days postoperation but may occur > 2 years delay
  • 3-phase bonescan: Diffuse increased activity on all phases in early infections; may be more focal in later presentation

– Loosening vs. infection: Delayedphaseimaging only or 3-phase imaging cannot reliably differentiate aseptic loosening from infection

– In-111 leukocyte imaging with Tc-99m sulfur colloid
provides most specific and accurate assessment for
joint infection and is diagnostic test of choice
– Diffuse periprosthetic uptake of tracer suggests
osteolysis from infection or loosening

– On SPECT, osteomyelitis is likely when uptake of In- 111 WBC localizes to bone on 2 or more adjacent tomographic slices
– False-negative results occur in chronic infections
– False-positive results occur in aseptic inflammation

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27
Q

Periprosthetic Soft Tissue Complications

A

• Pseudotumor (e.g.,particledisease), periprosthetic effusions, synovitis/bursitis
○ Bonescan may be positive in first 2 phases but weakly
increased or absent in 3rd phase; usually diagnosed by
CTorMR
• Snapping hip syndrome: Iliopsoas tendon may be evaluated dynamically with fluoroscopic tenography

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28
Q

Heterotopic Ossification

A
  • Bone formation in periprosthetic soft tissues commonly seen post operation due to liberation of primitive bone- forming cells
  • 3-phase bone scan: Focal mildly increased activity in soft tissues with corresponding new bone on radiograph
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29
Q

Joint infection protocol

A

– According to SNMMI, 15% window at 140-keV Tc-99m peak and a 15% window at 247-keV In-111 photopeak are used if Tc-99m dose is injected on day 1 before In- 111 leukocyte imaging

– 10% or 15% window at 173-keV In-111 photo peak for delayed In-111 leukocyte images obtained on day 2 (18–30 h) after Tc-99m dose has been injected

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30
Q

3 Phases of Bone Scan

A
  1. Angiographic phase - 2 sec planar images for 60 seconds in anterior and posterior projections. Assesses hypervascularity
  2. Blood pool phase - static planar images over area of interest. Assesses tissue hyperemia.
  3. Delayed phase +/- SPECT/CT. Assesses bone formation.
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31
Q

Osteomyelitis ddx

A
  1. Arthropathy (OA, Rheumatoid, Gout, neuropathic)
  2. Post-traumatic
  3. Paget’s
  4. Osteoid osteoma

• RecommendI n-111 WBC with Tc-99m SC after abnormal 3- phase bone

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32
Q

Septic arthritis findings

A

Activity on both sides of joint

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33
Q

Primary hyperparathyroidism findings

A

– Normal bone scan in 80%
– Foci of increased uptake: Calvarium, mandible,
sternum, acromioclavicular joint, lateral humeral
epicondyles, hands
– Increased uptake in brown tumors

– Extraskeletal uptake
□ Lungs, kidneys, stomach most common
□ Myocardium, spleen, diaphragm, thyroid, skeletal
muscle in severe disease

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34
Q

Secondary hyperparathyroidism findings

A

– Superscan
– Diffuse lung uptake in 60%
– Brown tumors: Less common than in primary HPT
– Uptake increased in vertebrae, distal 3rd of long
bones, rib

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35
Q

Osteomalacia findings

A

○ Generalized increased uptake in axial skeleton
○ Increased uptake at ends of multiple ribs, with beading
appearance along rib cage (rachitic rosary sign)
– In contrast to linear orientation of metastasis along
single rib

○ Increased sternum uptake common
○ Pseudofractures (Looser zone or Milkman fractures)
occur in ribs, lateral scapula, clavicles, pubic rami,

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36
Q

Renal osteodystrophy

A

○ Can have very high bone: soft tissue ratio,s imilar to
superscan
– Typically most striking appearance of metabolic bone
diseases excluding Paget disease
– Lack of bladder activity can help differentiate from
metastatic superscan
○ Signs of secondary HPT
○ More diffuse and symmetric than secondary HPT,which
may show focal uptake from cystic changes and brown
tumors

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37
Q

Heterotopic ossification classification

A
  • Acquired: Ectopic ossification, myositis ossificans circumscripta/traumatica
  • Hereditary: Atraumatic HO, fibrodysplasia ossificans progressiva (FOP)/myositis ossificans progressiva (MOP), Münchmeyer disease
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38
Q

Heterotopic ossification findings

A

○ Positive on angiographic, blood pool, delayed bone scan phases during formation, maturation

○ Moderately positive on delayed phase only when lesion
becomes stable: Useful to monitor maturation

○ At maturation (6 months to 2 years), lesion matches or is similar to normal bone (i.e., vertebral body) on bone scan

Conventional modalities should demonstrate peripheral to central ossification, central fat in mature lesions

39
Q

HO ddx

A

Hematoma - Non enhancing centrally (in contrast to early HO onMR)

DVT

Extraskeletal (Parosteal) Osteosarcoma, Synovial
Sarcoma, Chondrosarcoma - HO should have soft issue plane between adjacent bone

Tumoral Calcinosis

40
Q

Acute fracture findings

A

Positive on all 3 phases

41
Q

Subacute fracture findings

A

↓ in activity on blood flow and blood pool images with ↑ localization at fracture site

42
Q

Wolf law

A

Bone remodels in response to stress

43
Q

Stress fracture locations

A

Most common: Tibialshaft (posteromedial cortex of
distal 1/3); running, activity requiring rapid
decelerations/stops
– Anterior tibial stress fractures uncommon: African
American athletes, marching in sand, telemark skiers;
mimics direct contusion
– Tarsal bones: Calcaneus (vertically oriented, parallel to
physeal scar), talus, navicular
– Metatarsals, particularly 2ndand3rd: Walking,
marching, endurance sports, ballet
– Fibula: Marathon running, jumping, ballet
– Spine: Pars, pedicles; spondylolysis may occur in young
athletes (L5 > L4 > L3); may be incomplete or
unilateral; younger patients more likely asymptomatic
– Sacrum: More common than other pelvic sites; H
configuration due to vertical and horizontal fractures
implies insufficiency fracture
– Pelvis: Pubic rami/symphysis pubis, also iliac or supra-
acetabular
– Femur: Most common in medial femoral
neck/intertrochanteric region; distal femur most
common posteriorly (lateral images helpful)
– Sesamoids: Running, jumping; DDx: Sesamoiditis
– Occasionally humerus, radius, ulna, scapula, ribs

44
Q

Stress fracture findings

A

Typically positive on all 3 phases

45
Q

DDx stress fracture`

A
  1. Shin splints - • Linear, superficial posterior medial tibial cortex, ≥1/3 of tibial length. Angiographic and blood pool phase typically normal.
  2. Soft tissue pathology - Strains, sprains, contusions, myositis, endinopathies, neuropathies, compartment syndromes
  3. Trauma
  4. Neoplasm
46
Q

AVN locations

A
○ Commonly anterior weight-bearing portion of femoral
head, and humeral head
○ Scaphoid
○ Knee: Medial femoral condyle (Blount disease) in
pediatrics; idiopathic osteonecrosis (elderly females)
○ Lunate (Kienböck disease)
○ Tarsal navicular (Köhler disease)
○ Talus
○ Proximaltibia
○ Vertebrae (Kummel disease)
○ Small bones of hands and feet
○ Pelvis
○ Metatarsal head (Freiberg disease)
47
Q

Bone scan findings AVN

A

○ Vascular phase of AVN
– Photopenic defect
– May have donut sign due to surrounding hyperemia,
adjacent synovitis

– SPECT/CT imaging helpful in unmasking hyperemia
from avascular area

○ Reparative phase of AVN – Photopenia diminishes
– Increased activity due to osteoblastic response

Use high resolution/pinhole collimators or SPECT

48
Q

SC for AVN

A

○ Defines distribution of viable red bone marrow (marrow map), reticuloendothelial system
○ Symptomatic sites of AVN: Decreased activity immediately after vaso-occlusive event
○ Asymptomatic sites of AVN:Decreased activity in area of old bone infarct
○ Useful in identifying patients with expanded marrow, such as sickle cell patients

49
Q

AVN Ddx

A

Fracture
Transient osteoporosis
Infection
Neoplasm - lytic or sclerotic met or bone primary

50
Q

CRPS type 1

A

No detectable nerve lesion

51
Q

CRPS type 2

A

Detectable nerve lesion

52
Q

CRPS stages

A

Stage 1
Extremity pain characterized - throbbing, burning, cold/touch intolerance, swelling

Stage 2
Muscle wasting, ↑soft tissue edema, brawny skin, ↑ pain, vasomotor abnormalities

Stage 3
↓range of motion, digit/joint contracture, waxy skin, brittle, ridged nails, vasomotor abnormalities,↓ pain

53
Q

CRPS findings

A

Classic findings on 3-phase bone scan
○ Angiographic phase: Hyperperfusion to affected limb
○ Blood pool phase: Periarticular hyperemia when
compared with unaffected limb
○ Delayed phase: Increased periarticular activity in affected limb; abnormal activity increases distally

Can be intense knee, ankle uptake

54
Q

CRPS ddx

A

Disuse - more pronounced proximally instead of distally

Neuropathy -

Vascular - vasculitis, Raynaud’s, venous thrombosis

55
Q

Sickle Cell findings

A
  • Bone infarction: ↓activity on bone scan if acute; may have no or mild uptake on leukocyte scan
  • Osteomyelitis: ↑activity on 3-phase bone scan and leukocyte scan
  • Generalized ↑ uptake in skeleton often seen 2° to chronic anemia → marrow expansion
  • Spleen may show extraosseous uptake 2° to infarction, calcification, and fibrosis
  • Bone infarction: Axial skeleton and long bones most frequently involved (hematopoietic bone marrow)
  • Osteomyelitis: Hematogenous spread to vascular bone, usually in long bones (tibia, femur, humerus)
56
Q

Ankylosing spondylitis

A

Multilevel confluent uptake within spine - active bony bridging

57
Q

Gout

A

Intense activity, can be segmental. Ddx Septic arthropathy

58
Q

Heterotopic ossification

A

Consider when diffuse soft tissue uptake surrounding hip or elbow

Ask for different views to be sure in soft tissue and not bone

59
Q

Shin splints

A

Linear tibial activity, usually posteromedial

60
Q

Pars stress fracture

A

“AKA pars defect”, focally hot on MDP if acute

61
Q

Ddx myocardial uptake on bone scan

A

Myocarditis
Amyloid
Infarct (shouldn’t involve whole ventricle)
Cardiomyopathy

62
Q

Ddx muscle uptake on bone scan

A
Rhabdomyositis
Polymyositis/dermatomyositis
Ischemia
Trauma
Myositis ossificans/heterotopic calcification
Tumoral 
Tumours
63
Q

Primary and metastatic tumours with increased MDP uptake

A
Osteosarcoma
Lung
Breast
Prostate
Colon
64
Q

Diffuse lung activity on bone scan

A

Malignant pleural effusion
Fibrothorax
Radiation induced pneumonitis

65
Q

Enlarged spleen on bone scan in a child

A

SS
Thalassemia
Hemosiderosis

Look for bone findings to support infarcts

66
Q

Ddx frostbite

A

Vascular insufficieny
Previous surgery
Acute osteomyelitis
Tumour replacement

67
Q

Frieberg’s

A

AVN metatarsal head

Ddx fracture, osteomyelitis, hypervascular tumour,

68
Q

Causes AVN

A
Trauma
SSD
Alcoholism
Pancreatitis
CVD
Hypercortisolism
69
Q

McCune-Albright

A

Polyostotic fibrous dysplasia
Precosious puberty
Pigmented skin lesions

70
Q

Metabolic superscan

A
Primary/secondary (more likely to have osteosclerosis) hyperparathyoidism
Diffuse metastases
Myelofibrosis
Mastocytosis
Flourosis
HOA
Thyroid acropachy
Melorheostosis
71
Q

Solitary cold lesion ddx

A

Primary neoplasm (benign - hemangioma, malignant)
Metastasis/MM/plasmacytoma/brown tumour HPT
Overlying attenuation

72
Q

Ddx Metastatic bone scan

A

Metabolic superscan - entire skeleton

Multifocal paget’s

73
Q

HOA ddx

A

Diffusely increased cortical and periosteal uptake involving the extemities

Ddx: 
Shin splints
Paget's
Venous insufficiency
Thyroid acropachy
74
Q

Shin splints vs stress fracture

A

Linear vs focal
Hot on delayed only vs hot on all 3 phases

Ddx: met, infection

75
Q

Ddx Infected prosthesis

A

Normal healing
Infection
Prosthetic loosening
Normal marrow packing

76
Q

Sacral insufficiency fracture ddx

A

Sacroiliitis

Metastases

77
Q

Stomach, lung, heart uptake on bonse scan

A

Ddx:
Hypercalcemia - primary or secondary hyperparathyroidism
Free pertechnetate
Mucinous metastases

78
Q

AVN differential (cold hip or shoulder)

A

Septic arthritis
Tumour

Do high res pinholes

79
Q

Ddx metastatic disease on bone scan

A

Multifocal Paget’s

Multiple bone lesions associated with a metabolic disorder like hyperparathyroidism

80
Q

RSD Ddx

A

Inflammatory arthritis - look at pattern of joint involvementn

Osteomyelitis - unusual to be so mltifocal

81
Q

Ddx skull uptake

A

Metastasis
Craniotomy defect
Extraosseous uptake - meningioma

82
Q

Ddx sickle cell

A

Metastatic disease

Benign polyostotic process - fibrous dysplasia, enchondromas,

83
Q

Hot midfoot on all three phases

A

Acute fractures
Osteomyelitis/septic arthritis
Charcot arthropathy

84
Q

Metastatic calcifications of hyperparathyroidism

A

Tracer within stomach, lungs, kidneys

85
Q

Myocardial tracer activity on bone scan

A

Amyloid
Myocarditis/pericarditis
Recent MI
Recent myocardial perfusion study

86
Q

Diffuse calvarial activity

A

Paget’s
Metastatic disease
Post-radiation changes
Inflammation in adjacent soft tissues

87
Q

Sickle cell

A

Marrow expansion/increased activity in:
Diploic space of skull
Metaphyses of long bones
Spleen

Need additional gallium or WBC scan if suspect osteomyelitis

88
Q

Diffusely increased abdominal activity

A

Ascites/exudative effusion
Peritoneal carcinomatosis
Recent radiotracer with GI elimination

89
Q

RUQ uptake on bone scan

A

Hepatic metastases
Prior sulphur colloid scan
Colloid formation during radiopharamaceutical prep
Hepatic necrosis

90
Q

Subcutaneous soft tissue/muscle uptake ddx

A
Soft tissue metastases
Cellulitis/Abscess
Soft tissue trauma
Heterotopic ossification
Primary soft tissue tumour
Contamination
91
Q

Focal uptake at tip of hip prosthesis

A

If cemented - when accompanied by clinical symptoms is suspicious for loosening

If non-cemented - Most likely due to normal osteoblastic remodelling. Can remain hot for years.

92
Q

Spondylolysis ddx

A

Trauma
Osteomyelitis
Metastases

93
Q

Ddx osteosarcoma on bone scan

A
Primary bone tumour (benign/maligant)
Metastasis
Fracture
Osteomyelitis
Bone infarct