Tumors Flashcards
MC overall malignancy
Metastatic disease
MC primary malignant bone tumor in adult
Multiple Myeloma
MC primary malignancy tumor in kids/young adults
Osteosarcoma
2nd MC primary malignant tumor in adults
Chondrosarcoma
2nd MC primary malignant tumor in kids
Ewing sarcoma
Mc benign spinal tumor
Hemangioma
Mc benign bone tumor
Osteochondroma
Mc benign tumor of the sacrum
Giant cell tumor
Mc benign tumor of the hand
Enchondroma
Buttressing. And associated with what?
Additional layers of new bone added to exterior creating an expanded ossueous contour
Associated with slow growing lesions
Laminated/layered/onion skin. And associated with hat
Alternating layers of lucency and opacity with alternating growth. Thick or thin.
Can be seen in slow or aggressive lesions . Classic with Ewing’s
Colman’s triangle and speculated periosteum reaction often associated with what
Osteosarcoma
Reasons for missing pedicle
- Congential
- Destructive
- tumor (primary: ABC/osteoblastoma; secondary: lyric Mets MC!!!!; ST tumor: neurofibroma)
- infection - Surgical
DDx for ivory vertebra
Lymphoma
Blastic mets
Pagets
20-40: mc lymphoma
40+: mc blastic Mets
DDx for pathological collapse
OP
Lytic Mets
MM
Child: mc eosinophilia granuloma
Tests for MM
PEP
Skeletal survey
MRI
Biopsy
Tests for lytic Mets
Bone scan
MRI
What do carcinomas arise from?
Epithelial cells
What do sarcomas arise from?
Bone, cartilage, fat, muscle, blood vessels, or other connective or supportive tissue
Description of cartilaginous matrix
Ring or arc like Flocculent Small crystals Popcorn like Stippled
Pathway of metastasis
Hematogenous dissemination (blood) via Batson’s plexus aka vertebral plexus
Alkaline phosphatase will be increased in what kind of CA?
Blastic
Where in the skeleton does Mets usually spread
Spine (40)
Ribs/sternum (28)
Pelvis/sacrum (12)
Mets distal to elbow and knee is termed what and due to what?
Acral metastasis
Due to lung primary
Blow out mets MC from what
Renal or thyroid
MC reason for pedicle destruction
Lytic mets
Radiographic features of vertebral mets
Ivory vertebra Pedicle destruction Pathological collapse (OP, LM, MM) Focal OP Malignant schmorl node formation
T1 and T2 determining old vs new pathological fractures
“T1 white is right”
New: T1 dark, T2 bright
DDX for ivory vertebra
Paget
Hodgkins Lymphoma
Osteoblastic mets
Area of dense sclerosis on the anterior superior VB without sclerosis
Blastic mets
Bone island. Alt Ddx?
Blastic density that is longitudinal. Normal alkaline phosphatase levels and bone scan
Ddx: blastic mets
Osteopoikilosis
Multiple bone islands
Usually in pelvis
What does patient need to diagnose blastic mets
BCP for alkaline and acid phosphatase levels
PSA
Digital rectal exam
Avulsion fracture of lesser trochanter. MC diagnosis in child? Adult?
Child: avulsion Fx
Adult: lytic mets
Top 4 primary malignancies in order
Multiple myeloma, osteosarcoma, chondrosarcoma, Ewing sarcoma
(MOCE)
Malignant proliferation of plasma cells that infiltrate bone marrow
MM
Age of patients with MM
50-70
Clinical s/s of MM
Pain is cardinal sign
CRAB
(Hypercalcemia, renal/respiratory disease, anemia, bone disease)
Major lab findings with MM
M-spike A:G ratio (increased G) Bence Jones Rouloux formation Increased serum ca++ and protein Bone marrow biopsy >10% plasma cells
Osteosarcoma. Stats/age
Mc primary malignant BT in child. (#2 MBT). 10-25
Location of osteosarcoma
Metaphysis
Raindrop skull
MM
Bones affected by MM
T/L vertebra, pelvis, skull
Area MM
Diaphysis
Age of osteosarcoma
10-25, 60+
Area of osteosarcoma
Metaphysis
Bone affected by osteosarcoma
Distal femur 40%
Prox tibia 15%
Humerus
Appearance of osteosarcoma
50% sclerotic More than 5cm in medullary space Sunburst periosteal reaction/Codmans Large ST mass Painful swelling Cumulus/cloud-like density
MRI characteristics of mets
Dark T1
Light t2
Bones affected by MM
Vertebra-T, L
What are the two bone tumors that occur solely in the diaphysis
MM
Ewing sarcoma
Solitary plasmactyoma findings
Soap bubbly
Highly expansive
Vertebra>pelvic>skull
What tumors have blastic appearances
Osteosarcoma
Osteoma
What tumor usually has mets to lungs before being discovered
Osteosarcoma
Age for chondrosarcoma
50+
Locations for chondrosarcoma
Proximal humerus
Neck/femur
Ribs/sternum
Pelvis**
XRAY of chondrosarcoma
Round area of de-mineralization
Popcorn matrix calcification
Large soft tissue mass
Ddx for chondrosarcoma
Enchondroma
Medullary infarct
Both usually no pain
Age and bone location for Ewing
Diaphyisis
10-25
Bones in Ewing sarcoma
Long tubular bones (femur, tibia, humerus, fibula)
Flat bones >20yrs
Appearance of Ewing sarcoma
Lytic Moth eaten-permeating Onion skin reaction ST mass Cortical saucerization (scooped out of outer cortex)
Cortical saucerization
Scooped out appearance of outter cortex
Aka for giant cell
Osteoclastoma
Age and bone location for giant cell
20-40
Met-epiph
Location of giant cell
85% long bone: d. Femur, prox tibia, d radius (mc malignant)
XRAY of giant cell
Geographic Eccentric Met-epiph Subarticular Expansive/soap bubble Cortical thinning
Giant cell tumor where has highest chance of malignant transformation
Distal radius
Coat hanger exostosis
Solitary osteochondroma
Cauliflower cap
Solitary osteochondroma
Area in bone of osteochondroma
Metaphysis
Bones of osteochondroma
Long bones
Femur, tibia, proximal radius
Pain and new growth to an osteochondroma may indicate what
Malignant transformation to osteosarcoma
HME aka diaphyseal achalasia
Multiple osteochondromas
Age of osteochondroma and HME aka diaphyseal achalasia
2-20
Findings associated with HME
Madelung deformity/bayonet deformity: shortening of ulna and radius bend over it
Shortening of 4th.5th MC
Direction of pedunculated osteochondroma
Toward the mid shaft
Location in bone for SBC
Metaphysis
Age of SBC
3-14
Bones for SBC
Proximal humerus
Femur
Fibula
Calcaneous neck
Madelung/bayonet deformity
HME
Fallen fragment sign
SBC (solitary bone cyst)
XRAY of solitary bone cyst
Metaphysical Lucent 2-3cm Cone appearance/truncated Asymptomatic Central
Area in bone for ABC
Metaphysis
Age for ABC
10-30
Bones for ABC
Spine-30%
Neural arch
Long bones
Flat bone: P
XRAY for ABC
Eccentric
Lytic
Expansive/soap bubble
Pain
Fluid-fluid levels seen on CT
ABC
Osteoblastoma area in bone
Met-diaphyseal
Age of osteoblastoma
10-20
Bones of osteoblastoma
Neural arch
Long bones
Small bones of hands/feet
XRAY of osteoblastoma
Lucent
Expansive
>2cm
Metaphysical—> diaphyseal
Age of osteoid osteoma
10-25
Bone of osteoid osteoma
Long
Proximal femur***
Prox tibia
Neural arch—concave scoliosis
Location in bone for osteoid osteoma
Metaphysis-diaphysis
XRAY of osteoid osteoma
Nidus in cortex Lucent Geographic Cortical thickening Pain relieved by aspirin!!**
What tumor has pain relieved by aspirin
Osteoid osteoma
Nidus
Osteoid osteoma
Double density sign
Osteoid osteoma
Age of osteoma
Adult
Bones of osteoma
Frontal/ethmoid sinus
Calvarium
XRAY of osteoma
Blastic lesions
~2cm
Geographic
What tumor is associated with Gardner’s syndrome
Osteoma
Age of enchondroma
10-30
Bones of enchondroma
Hands/wrist phalanges>MC
Long bones
Area in bone of enchondroma
Metaphysis/diaphysis
XRAY of enchondroma
Lytic Expansive Geographic Central Stippled/punctuate calcification
5 tumors that have cartilage matrix
Osteochondroma Chondroblastoma Chondromyxoid fibroma Enchondroma Chondrosarcoma
Multiple enchondroma
Olliers/enchondromatosis
Olliers associated with multiple ST hemangioma
Maffucci syndrome
Age of hemangioma
30-50
Bones inhemangioma
Lower T, upper L vertebra
Calvarium
XRAY for hemangioma
≤Accentuated vertical trabeculation
Accordion/honeycomb/corduroy
Posterior bulge of cortex
Skull: <4cm round lytic lesioNS with sunburst appearance /spoke wheel
Spoke wheel appearance
Hemangioma
Accordion/corduroy/honeycomb appearance
Hemangioma
Age of chondroblastoma
5-25
Area in bone of chondroblastoma
Apophysis/epiphysis
Bones of chondroblastoma
2/3 LE
Prox femur, distal femur, proximal tibia
XRAY of chondroblastoma
Round lytic lesion Eccentric 1-6cm Geographic Lobulated Punctuate/ca++
Age of FCD
2-10
Bones of FCD
Long bones of LE
Post/med/distal femur
Area in bone of FCD
Metaphysis
XRAY of FCD
Lytic Geographic Central 1-2cm Expansive Sclerotic Asymptomatic
FCD or NOF—which is bigger?
NOF
age of NOF
8-20
Bones of NOF
Long bones of LE
Distal tibia
Area in bone of NOF
Metaphyseal
XRAY of NOF
Lytic Eccentric 2+cm Sclerotic boarder Asymptomatic Migrates toward diaphysis
Age of pagets
50+
Bones commonly affected with pagets
Pelvis
Lumbars/T
Femur
Calvarium
XRAY of pagets
Changed density Irregular trabeculation Thickened cortex Subarticular to diaphysis!!! Osseous deformity
Direction of pagets
Subarticular to diaphysis
Complications of pagets
Peripheral N compression Spinal stenosis Blind Facial palsy Pathological fx High CO DJD Malignant transformation —> osteosarcoma
What tumors may have malignant transformation to osteosarcoma
Paget
Olliers
Paget and ollier may have malignant transformation into what?
Osteosarcoma
Stage 1- pagets
Lytic/degenerative stage
Increased hydroxyproline
Stage 2 of paget
Mixed
Increased alkaline phosphatase
Stage 3 pagets
Sclerotic/ivory
Normal serum ca/P. Increased bone scan activity
Stage 4 paget
Malignant degeneration to osteosarcoma
Osteoporosis circumscripta
Well-defined lytic changes to frontal and occipital bone in pagets
Cotton wool appearance
Ill-defined density seen in pagets
Rim sign
Iliopectineal line thickening seen in pagets
What is seen in the pelvis wit pagets
Rim sign (iliopectineal line thickening)
Expansion
Acetabular protrusion
Candle flame/blade of grass sign
Advancing edge of lytic phase (toward diaphysis) seen with pagets
Looser lines/banana fx
Horizontal lucency/fx seen with pagets
Shepards crook
Bowing of prox femur head seen with paget and fibrous dysplasia
Brim sign
Iliopectineal line thickening seen with paget
Aka rim
Picture frame vertebra
Thickened endplates and cortex of VB in pagets
Ivory vertebra seen with
Paget
Blastic mets
Lymphoma
Fibrous dysplasia age
0-20
Bones in fibrous dysplasia
Monostotic
Proximal femur MC (also craniofacial bones)
XRAY of fibrous dysplasia
Lucent lesions Thick rim (Rind sign) Ground glass appearance of medullary Expansive in skull Shepards crook/sabreshin deformity Geographic
Fibrous dysplasia seen with cafe-au-last spots and endocrine dysfunction is what?
McCune Albright syndrome
McCune Albright syndrome
Fibrous dysplasia with cafe-au-lait spots, and endocrine disruption
Rind sign
Fibrous dysplasia
Medullary cavity lesions with a thick or thin rim of sclerosis
Complications of fibrous dysplasia
Leg length discrepancy Osseous deformities CN compromise Acetabular protrusion Pro ptosis (eyes bulging) Malignant transformation (fibrosarcoma)