Orthopaedic oncology Flashcards
What is a tumour?
- 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
Tumours can be divided into?
- Benign- remain localised single masses
- malignant tunours- invade surrounding tissues
What is important to check on a history of possible tumour?
- Pre-exisiting malignancy
- previous radiotherapy tx
- smoking
- peristent pain ( esp night)
- swelling
- night sweats
- weight loss
- altered sensation
What tumours give rise to mets in bone?
- Breast
- Bronchus
- Prostate
- Kidney
- Thyroid
- Melanoma
most osteolytic except Prostate which is sclerotic
What investigations are included is a neoplasia is suspected?
- 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
What do benign lesion show on plain xrays?
- Bone reaction at the margin -> a well demarcated appearance with a narrow zone of transmission
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What do maligant lesion show on plain xrays?
- 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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Can do you describe common locations of certain tumours?
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Describe the prinicples of tissue biopsy?
-
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%
- open preferred
-
Performed by treating surgeon at treating centre
- complx rate x5-12 when preformed by other surgeon, 20% tx compromised by biopsy
Describe the biopsy technique?
-
Preop
- tumour staging
- MSK team review
- treating surgeon does biopsy
- pathologist available for FF samples
- no tourniquet
- no antibiotics - infection always in DDx
-
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
-
approach
-
Post operative
- very careful post op path fx changes outcome
- team approach on review of results for best outcome and future tx
Can you describe the different factors invovled in the Enneking staging of tumours?
-
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
-
G1
-
Site
- T1 =Intracompartmental
- T2- extracompartmental
-
Mets
- Mo= No mets
- M1= mets present
Can you decribe the different enneking staging of tumours?
-
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
What are the different options for tumour excision?
-
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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what is the aim of treatment of tumour?
- Irradicate tumour but
- Preserve function
What are the indictions for ampuation?
- 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
What are the options for limb salvage?
-
Endoprosthesis
- massive endoprosthetic replacement
- custom made
- growing endoprosthetic
- massive endoprosthetic replacement
-
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
What condition uses adjuvant and neodajuvant chemo?
- OSteosarcoma
- Ewing’s
- neoadjuvant chemo post surgical ressection has demonstrated to improev survivorship
What condition uses radiotherapy?
- 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)