Orthopaedic oncology Flashcards

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1
Q

What is a tumour?

A
  • is a mass of tissue formed as a result of abnormal,excessive and inappropriate proliferation of cells, the growth of which continues idefinitely regardless of the mechanism that control normal cellular proliferation
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2
Q

Tumours can be divided into?

A
  • Benign- remain localised single masses
  • malignant tunours- invade surrounding tissues
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3
Q

What is important to check on a history of possible tumour?

A
  • Pre-exisiting malignancy
  • previous radiotherapy tx
  • smoking
  • peristent pain ( esp night)
  • swelling
  • night sweats
  • weight loss
  • altered sensation
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4
Q

What tumours give rise to mets in bone?

A
  • Breast
  • Bronchus
  • Prostate
  • Kidney
  • Thyroid
  • Melanoma

most osteolytic except Prostate which is sclerotic

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5
Q

What investigations are included is a neoplasia is suspected?

A
  • FBC
  • CRP/ESR
  • Serum electrophoresis
    • Multiple myeloma ( bence jone- proteins urine)
  • U& E, LFT’s
    • basline line but also elevated alk phosphatase in osteosarcoma.prostae specific antigen
  • Plain xrays
  • MRI
  • CT- lesion and chest/abdo/pelvis for staging
  • Tissue biopsy and histological analysis
  • Bone scan- to detect skip lesions- ewing’s sarcoma
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6
Q

What do benign lesion show on plain xrays?

A
  • Bone reaction at the margin -> a well demarcated appearance with a narrow zone of transmission
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7
Q

What do maligant lesion show on plain xrays?

A
  • due to rapid growth they allow little bone forming reponse to develop.
  • these lesions are poorly demarcated , permeative appearance with a wide zone of transmission
  • osteosarcomas may elevate periosteum so quickly that bone deposition is allowed only at margin = Codman’s triangle
  • Some attempt at bone formation by the periosteum overlying the lesion may -> streaks of calcification = sunray spiculations
  • more agressive lesions from within the medulla->cortical resorption= endosteal scalloping
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8
Q

Can do you describe common locations of certain tumours?

A
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9
Q

Describe the prinicples of tissue biopsy?

A
  • Provide a representative sample
    • for benign/malignant
    • to determine cell line
    • to grade lesion
  • Not to compromise future surgery
  • Timing
    • ​to do after investigation unless dx known
  • Open vs closed
    • open preferred
      • adv:more tissue, low sampling error
      • dis:larger field to excise later,higher local complx- infection
    • needle biosy: less tissue to excise later/less expensive
      • dis: accuracy 70-88% cf open 95%
  • Performed by treating surgeon at treating centre
    • complx rate x5-12 when preformed by other surgeon, 20% tx compromised by biopsy
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10
Q

Describe the biopsy technique?

A
  1. Preop
    • tumour staging
    • MSK team review
    • treating surgeon does biopsy
    • pathologist available for FF samples
    • no tourniquet
    • no antibiotics - infection always in DDx
  2. Operative
    • approach
      • plan w future op in mind
      • all aspects of biopsy tract must be excised
      • incision incorop into definitive surgery
      • incision longitudinal, no tissue undermining
      • only enter one compartment/ trans muscular
      • don’t expose NV structures
      • meticulous haemostasis
    • biopsy
      • round cortical windows- reduce stress risers
      • swab taken for MCNS
      • tissue for FF section/ histology
      • no closure until DW pathologist on phone
      • esure they have enought to make definitive dx/stage etc
    • closure
      • ​plug bone with PMMA/minimise tumour spread
      • achieve haemostasis
      • closure in layers
      • drain exit site in line with incision & thru wound
      • subcuticular suture to skin
      • firm dressing
      • immobilise
  3. Post operative
    • ​​​very careful post op path fx changes outcome
    • team approach on review of results for best outcome and future tx
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11
Q

Can you describe the different factors invovled in the Enneking staging of tumours?

A
  • Grade
    • G1
      • low grade
      • low risk of mets
      • well differentiated
      • few mitotic figures
      • moderate cytological atypia
    • G2
      • high grade
      • higher incidence of mets
      • poorly differentiated
      • high mitotic rate
      • high cell /matrix ratio
      • necrosis
      • microvascular invasion
  • Site
    • T1 =Intracompartmental
    • T2- extracompartmental
  • Mets
    • Mo= No mets
    • M1= mets present
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12
Q

Can you decribe the different enneking staging of tumours?

A
  • Stage 1A
    • low grade G1
    • T1 - intracompartmental
    • Mo
  • Stage 1B
    • Low grade G1
    • T2- extracompartmental
    • Mo
  • Stage 2A
    • High grade G2
    • T1
    • Mo
  • Stage 2B
    • High grade G2
    • T2
    • Mo
  • Stage 3
    • M1
    • Any grade and site
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13
Q

What are the different options for tumour excision?

A
  • Intralesional
    • path of excision passes thru the pseudo-capsule and directly thru lesion
    • entire operative field is considered potentially contaminated
  • Marginal
    • entire lesion is excised as one peice
    • plane of dissection in pseudo-capsule
  • Wide
    • lesion is removed with pseudocapsule and cuff of normal tissue
    • aka en bloc resection
  • ​Radical ( extracompartmental)
    • ​entire lesion and its structure of origin are removed
    • plane of dissection is outside the limiting fascia or bone
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14
Q

what is the aim of treatment of tumour?

A
  • Irradicate tumour but
  • Preserve function
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15
Q

What are the indictions for ampuation?

A
  • Pts in whom perivascular or neurological invasion renders resection of the tumour impossible without sacrifing distal function or viability
  • pt in whom tumour excision including biopsy tracts cannot be achieved without extensive excision of muscle
  • Pathological fx where there has been significant contamination by the tumour
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16
Q

What are the options for limb salvage?

A
  • Endoprosthesis
    • massive endoprosthetic replacement
      • custom made
      • growing endoprosthetic
  • Autograft
    • when only resection of diaphsyeal bone is required may use strut graft ( fibula)
    • excision , irradiation then implantation ( pelvic ring)
  • Allograft
    • large bulk of bone may be non viable
    • risk of disease transmission
    • availability of cadervic bone
17
Q

What condition uses adjuvant and neodajuvant chemo?

A
  • OSteosarcoma
  • Ewing’s
  • neoadjuvant chemo post surgical ressection has demonstrated to improev survivorship
18
Q

What condition uses radiotherapy?

A
  • for primary and soft -tissue tumour resection where a histological marginal resection is demonstrated or where pt factors limit the surgical resection can be achieved.
  • use for bone mets and pathological fx after stabilisation
  • Osteosarcoma
  • little effect with chondrosarcomas ( also no effect with chemo)