Primary + Secondary bone tumours Flashcards

1
Q

Do sclerotic or lytic lesions mean benign/malignant?

A

Sclerotic = healed or benign

Lytic = malignant

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

____ level is a marker of osteoBLAST activity?

A

ALP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How to tell on an X-ray if something is a tumour of bone or cartilage?

A

Cartilage: popcorn stippling / rings and arcs e.g. chondrosarcoma

Bone: fluffy/trabecular

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Stages of the periosteal reaction and what they tell you about the tumour?

A
  1. Callus - slow growing
  2. Lamellated / onion skinning - slow growing but definitely a tumour - Ewing’s tumour
  3. Sunburst spicules, codmans triangle -> an aggressive tumour e.g. osteosarcoma
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What does the zone of transition tell you?

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Define sarcoma.

A

A rare tumour of mesenchymal origin: a malignant connective tissue neoplasm.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Soft tissue sarcomas make up what percentage of overall sarcomas?

A

80%. The remaining 20% are boney.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Name 3 soft tissue sarcomas.

A
  1. Liposarcoma.
  2. Leiomyosarcoma.
  3. Rhabdomyosarcoma.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is liposarcoma?

A

A malignant neoplasm of adipose tissue.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is leiomyosarcoma?

A

A malignant neoplasm of smooth muscle.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is rhabdomyoscarcoma?

A

A malignant neoplasm of skeletal muscle.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Name 4 primary bone tumours / boney sarcomas.

A
  1. Osteosarcoma.
  2. Ewing’s sarcoma.
  3. Chondrosarcoma.
  4. Fibrosarcoma.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Primary bone tumours originate from the _____ tissue.

A

mesenchymal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is osteosarcoma? Give 3 features of osteosarcoma.

A

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.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is osteochondroma? Give 3 features.

A
  • 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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is an Ewing sarcoma? Give 3 features.

A

Malignant
Bone marrow
Mesenchymal stem cells/neuroectodermal cells
Very young
Lamellated bone
Can compress nerves
Lytic bone lesions, onion skinning

17
Q

Name a boney sarcoma that responds well to chemotherapy.

A

Ewing’s sarcoma.

18
Q

Give 2 red flag symptoms for sarcoma.

A
  1. Non mechanical pain.
  2. Pain at night.
19
Q

Give 5 symptoms of a bone tumour.

A

Constant, non mechanical bone pain
Swelling
Fracture
B symptoms - fever, night sweats, malaise
Avascular necrosis
Symptoms of nerve compression - numbness/weakness

20
Q

Give 4 signs that suggest malignancy and can be used to make a diagnosis of soft tissue sarcoma.

A
  1. Lump > 5cm.
  2. Lump is increasing in size.
  3. Lump is deep to fascia.
  4. Pain.
21
Q

What investigations might you do in someone who you suspect to have a sarcoma?

A
  1. MRI.
  2. Core needle biopsy.
  3. CT scan.
22
Q

What is the treatment for sarcomas?

A
  1. MDT meeting.
  2. Surgery for localised soft tissue sarcomas; ensure a wide margin.
  3. Amputation.
  4. If non resectable, chemotherapy and radiotherapy.
23
Q

If it is not possible to get a wide margin when resecting a sarcoma, what might you do?

A

Give adjuvant radiotherapy.

24
Q

Which tumours can metastasise into bone tumours? Give 5.
HINT: Mnemonic

A

Mnemonic - PB-KTL - ‘Lead kettle’:
P: prostate
B: breast
K: kidney
T: thyroid
L: lung

25
Q

What is myeloma?

A

Abnormal proliferation of a single clone of plasma cells, leading to production of monoclonal immunoglobulins (IgG or IgA).

26
Q

What are the diagnostic criteria for myeloma?

A

2 out of 3:
1. Paraproteinaemia on serum protein immunofixation or Bence Jones proteins in urine.

  1. Radiological (MRI/CT) evidence of lytic bone lesions.
  2. Increase in bone marrow plasma cells - bone marrow aspiration/biopsy.
27
Q

Describe the clinical features caused by osteolytic bone lesions in myeloma.

A

Backache.
Pathological fractures (e.g. long bone, ribs).
Vertebral collapse.
Hypercalcaemia.

28
Q

What other clinical features, apart from those associated with osteolytic bone lesions, may be present in a myeloma patient?

A

Anaemia, neutropenia or thrombocytopenia (due to marrow infiltration) - anaemia symptoms, infections and bleeding.

Renal impairment due to light chain deposition in tubules.

29
Q

What would blood tests show in a myeloma patient?

A

Normocytic, normochromic anaemia, thrombocytopaenia, leukopaenia.

ESR high.

U&Es:
Raised Calcium
Raised Urea + creatinine

Hypercalcaemia.

30
Q

What would be found in the urine of someone with myeloma?

A

Bence Jones proteins - paraproteinaemia leads to excretion of kappa/lambda light chains in urine

31
Q

Serum ____ is high in secondary bone tumours.

A

calcium

32
Q

How would myeloma be treated?

A

Analgesia → bone pain
Bisphosphonates → e.g. Alendronate -> reduce fractures and bone pain
Local radiotherapy → reduce focal disease
Transfusion → correct anaemia
Fluids/ dialysis → manage renal failure
Abx for infections
Chemotherapy
- melphalan + prednisolone, or VAD (vancristin, adriamycin + dexamethasone), if fit.