2. MSK p194-198 (Aggressive Lesions) Flashcards

Bone Tumours

1
Q

Commonest primary osseous malignancies (3)

A

1) Myeloma/plasmacytoma (27%)
2) Osteosarcoma (20%)
3) Chondrosarcoma (20%)

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2
Q

Osteosarcoma - Subtypes

A

Conventional intramedullary (85%)
Paraosteal (4%)
Periosteal (1%)
Telangectatic (rare)

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3
Q

Conventional Intramedullary Osteosarcoma (general info)

A

Higher grade than surface subtypes
Typically younger pt (10-20)
Typically femur (40%) and proximal tibia (15%)

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4
Q

Periosteal reactions (buzzwords)

A

Sunburst - Agressive periosteal reaction, looks like sunburst
Codman triangle - New periosteum doesn’t have time to completely ossify, so only raised edge ossifies
Lamellated (onion skin) - multiple layers of parallel periosteum

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5
Q

High yield trivia (osteosarcoma)

A

Osteosarcoma met to lung is classic cause of occult pneumothorax
Reverse zoning - denser matrix in centre, less dense periphery

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6
Q

Risk factors for pathologic fractures (3)

A

1 - Lytic lesions
2 - Lesions >3cm in size
3 - Lesions involving >50% of cortex

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7
Q

Parosteal osteosarcoma (general) (5)

A

Low grade, bulky, parosteal bone formation.
BIG tumours.
Early adult/middle age.
Commonly posterior distal femur. 90% metaphysis.
String sign: radiolucent line separating bulky tumour from cortex.

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8
Q

Periosteal osteosarcoma (5)

A

Worse prognosis than parosteal, better than conventional intramedullary.
15-25YO.
More commonly diaphyseal.
Classically medial distal femur.
No marrow extension unlike parosteal (50%).

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9
Q

Telangectatic Osteosarcoma (general) (4)

A

15% have narrow zone of transition.
Fluid-fluid level on MRI is classic.
T1 bright (methaemoglobin).
Tumour nodularity and enhancement differentiates from CGT and ABC

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10
Q

Fluid-fluid levels DDx (3)

A

Telangectatic Osteosarcoma
Aneurysmal Bone Cyst
Giant Cell Tumour

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11
Q

Chondrosarcoma (4)

A

Usually older adults (M>F)
Flat bones, proximal tubular bones, limb girdles.
Central (intramedullary) or peripheral (end of osteochondroma)
Usually low grade

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12
Q

Chondroblastoma in adult

A

Clear cell chondrosarcoma

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13
Q

Ewings sarcoma (3)

A

Permeative lesion in the diaphysis of child
Usually mets bone to bone
Mimic osteosarcoma due to marked sclerosis (occurs in bone only, not soft tissue like osteosarcoma)

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14
Q

Chordoma (3)

A

Age 30-60, younger in clivus, older in sacrum
Very T2 bright
Sacrum > Clivus > Vertebral body

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15
Q

Chordoma trivia (3)

A

Commonest primary malignancy of spine or sacrum
Most common spinal location is C2
Almost always midline

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16
Q

Fibrosarcoma (4)

A

Can be primary or secondary (Pagets, infarct etc).
Lytic malignant tumours that DONT produce osteoid or chondroid matric.
Almost always lytic, may be permeative or moth eaten
NOT T2 bright (most tumours are)

17
Q

MFH (5)

A

Malignant Fibrous Histiocytoma (Now called Pleomorphic Undifferentiated Sarcoma (PUS)).
More common than fibrosarcomas, most common soft tissue sarcoma in adults.
Look radiologically similar to fibrosarcoma.
Bone infarcts can turn into MFH (Buzzword: Sarcomatous transformation of infarct)

18
Q

Synovial sarcoma - features (3)

A

Commonest in lower extremities of patients aged 20-40.
Close to (but not in) joint.
10% get secondary invasion into the joint (for multiple choice, they “never involve joint)

19
Q

Synovial sarcoma - imaging (3)

A

Triple sign
- High, medium and low signal in the same mass on T2 (usually knee)
Bowl of grapes
- Bunch of fluid-fluid levels in a mass (probably knee)
Plain film
- Soft tissue component with calcifications, least likely way to show it.

20
Q

Synovial sarcoma - trivia (6)

A

Most sarcomas don’t attach bones, these can.
Most present as painless mass, these hurt.
Soft tissue calcifications + bone erosions are highly suggestive.
Show growing & small, often lead people to call them benign.
90% have translocation of X-18.
Most common malignancy in teens/young adults of foot, ankle and lower extremity

21
Q

Ball like tumour in extremity of young adult

A

Synovial sarcoma

22
Q

Liposarcoma (4)

A

2nd commonest soft tissue sarcoma.
Common in middle aged, commonly in retroperitoneum (can also happen in extremities).
Most common type is well differentiated (least aggressive).
Fatty mass in the retroperitoneum = Liposarcoma

23
Q

Liposarcoma vs lipoma (3)

A

Imhomogenous attenuation - soft tissues masses in the fat
Infiltration of adjacent structures
Deep and big

24
Q

Myxoid liposarcoma (3)

A

Commonest liposarcoma in <20yo.
Can be T2 bright but T1 dark, not a cyst.
Needs gadolinium imaging

25
Q

Treeatment of agressive lesions (4)

A

Osteosarcoma - Chemo (to kill micro mets) then wide excision.
Ewings: Chemi and Radiation, then wide excision.
Chondrosarcoma: Usually just wide excision (low grade, main concern is local recurrence)
Giant Cell Tumour: Usually requires arthroplasty as it extends to articular surface.

26
Q

Myositis ossificans (3)

A

Circumferencial calcifications with lucent centre.
Can look scare on MRI if imaged early due to oedema and avid enhnacement.
Benign, don’t biopsy

27
Q

Avulsion injury (2)

A

Typically near pelvis, can have aggressive periosteal reaction.
Benign, don’t biopsy.

28
Q

Cortical desmoid (3)

A

Classically on posterior medial epicondyle of distal femur.
Can be hot on bone scan.
Benign, don’t biopsy.

29
Q

Synovial Herniation Pit (4)

A

Aka pitt’s pit.
Characteristic location in femoral neck.
Lytic appearing lesion.
Benign, don’t biopsy

30
Q

Bone biopsy (5)

A

D/W ortho to avoid contaminating parts not involved by tumour.
Pelvis: Avoid crossing gluteal muscles (may be needed for reconstruction).
Knee: Avoid joint space via crossing suprapatellar bursa or other communicating bursae.
Avoid crossing Quads tendon unless involved.
Shoulder: Avoid posterior 2/3 (axillary nerve courses post to anterior, therefore posterior resection will denervate antererior third)