Primary + Secondary bone tumours Flashcards
(32 cards)
Do sclerotic or lytic lesions mean benign/malignant?
Sclerotic = healed or benign
Lytic = malignant
____ level is a marker of osteoBLAST activity?
ALP
How to tell on an X-ray if something is a tumour of bone or cartilage?
Cartilage: popcorn stippling / rings and arcs e.g. chondrosarcoma
Bone: fluffy/trabecular
Stages of the periosteal reaction and what they tell you about the tumour?
- Callus - slow growing
- Lamellated / onion skinning - slow growing but definitely a tumour - Ewing’s tumour
- Sunburst spicules, codmans triangle -> an aggressive tumour e.g. osteosarcoma
What does the zone of transition tell you?
Wide zone of transition - means there is poor definition of healthy | not healthy - so more likely to be malignant
Narrow zone of transmission does not always mean benign, beware of myeloma esp. in old people
Define sarcoma.
A rare tumour of mesenchymal origin: a malignant connective tissue neoplasm.
Soft tissue sarcomas make up what percentage of overall sarcomas?
80%. The remaining 20% are boney.
Name 3 soft tissue sarcomas.
- Liposarcoma.
- Leiomyosarcoma.
- Rhabdomyosarcoma.
What is liposarcoma?
A malignant neoplasm of adipose tissue.
What is leiomyosarcoma?
A malignant neoplasm of smooth muscle.
What is rhabdomyoscarcoma?
A malignant neoplasm of skeletal muscle.
Name 4 primary bone tumours / boney sarcomas.
- Osteosarcoma.
- Ewing’s sarcoma.
- Chondrosarcoma.
- Fibrosarcoma.
Primary bone tumours originate from the _____ tissue.
mesenchymal
What is osteosarcoma? Give 3 features of osteosarcoma.
Bone forming (produce osteoid) and is malignant.
1. Fast growing.
2. Aggressive.
3. Typically affects 15 - 17 y/o - in the young.
4. ALP will be raised, as osteoblast hyperactivity.
What is osteochondroma? Give 3 features.
- Cancer of the cartilage
- Most common adult none sarcoma
- Associated with dull, deep pain and affected area is swollen & tender
- Common sites affected: pelvis, femur, humerus, scapula and ribs
What is an Ewing sarcoma? Give 3 features.
Malignant
Bone marrow
Mesenchymal stem cells/neuroectodermal cells
Very young
Lamellated bone
Can compress nerves
Lytic bone lesions, onion skinning
Name a boney sarcoma that responds well to chemotherapy.
Ewing’s sarcoma.
Give 2 red flag symptoms for sarcoma.
- Non mechanical pain.
- Pain at night.
Give 5 symptoms of a bone tumour.
Constant, non mechanical bone pain
Swelling
Fracture
B symptoms - fever, night sweats, malaise
Avascular necrosis
Symptoms of nerve compression - numbness/weakness
Give 4 signs that suggest malignancy and can be used to make a diagnosis of soft tissue sarcoma.
- Lump > 5cm.
- Lump is increasing in size.
- Lump is deep to fascia.
- Pain.
What investigations might you do in someone who you suspect to have a sarcoma?
- MRI.
- Core needle biopsy.
- CT scan.
What is the treatment for sarcomas?
- MDT meeting.
- Surgery for localised soft tissue sarcomas; ensure a wide margin.
- Amputation.
- If non resectable, chemotherapy and radiotherapy.
If it is not possible to get a wide margin when resecting a sarcoma, what might you do?
Give adjuvant radiotherapy.
Which tumours can metastasise into bone tumours? Give 5.
HINT: Mnemonic
Mnemonic - PB-KTL - ‘Lead kettle’:
P: prostate
B: breast
K: kidney
T: thyroid
L: lung