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INTRODUCTION TO BONE
TUMOURS
AND GCT
Dr. Lokesh Chugh
PG resident
GMC. Amritsar.
INTRODUCTION
• Bony lesions
• Arises from bone itself (primary)
• Arrived from distant sites (secondary)
• Benign
• Malignant
DIAGNOSTIC EVALUATION
• Adequate history, C/F
• Physical examination
• Radiological examination-benign vs malignant
• Biopsy- confirmatory
• pain, mass
• Surrounding muscle atropy – disuse of limb
• Neurological deficit- nerve involvement
• Café-au-lait spot- NF
• Lymph node metastasis- synovial sarcoma
MASS
• Consistency
• Mobility
• Tenderness
• Local temperature
• Dimensions
• Location
• Shape
• Change with position
RADIOGRAPHIC EXAMINATION
EPIPHYSEAL LESIONS - D/D
• Chondroblastoma (10-25yrs)-
central, can cross joint line
(benign)
• GCT (20-40 yrs)- eccentric, soap bubble
appaerance, never crosses joint line
(locally aggressive)
• Clear chondrosarcoma (rare)
(malignant)
DIAPHYSEAL LESIONS – D/D
• EWING SARCOMA (5-25 yrs)
(Onion peel )
• LYMPHOMA (ADULTS)
• FIBROUS DYSPLASIA (5-30yrs)
(Shepherd crook deformity)
• HISTIOCYTOSIS(5-30yrs)
SPINE LESIONS –D/D
≥40 yrs
• Metastasis
• MM
• Cordoma
≤ 30 yrs
• OO
• OB
• ABC
MULTIPLE LESIONS - D/D
• MM
• METASTASIS
• FD
• HEMANGIOMA
• INFECTION
• HYPERPTH
BENIGN VS MALIGNANT
• Low biological activity,
± surrounded by rim of
reactive bone
• Well marginated
• Narrow zone of
transition(long
standing, non aggresive)
• Geographical pattern of
osteolytic destruction
• High biological activity,
shows periosteal rxn
• Poorly marginated
• wide defined zone of
transition (fast growing,
aggressive)
• Non geographical/
poorly defined cortical
destruction
PERIOSTEAL REACTION
• New bone formation
• When tumour destroys the cortex
• CODMAN TRIANGLE -OS
• ONION SKINNING -ES
• SUN BURST APPEARANCE -OS
• D/D- malignancy, infection, histiocytosis
BONE MATRIX
• Calcific stippling- enchondroma, CS
• Matrix ossification- OS
• Ground glass app.- FD
TUMOUR STAGING
WHO CLASSIFICATION
Bone forming tumours
• Benign: - Osteoid osteoma, osteoma
- Osteoblastoma
• Indeterminate - Aggressive osteoblastoma
• Malignant - Osteosarcoma
conventional, variants
Cartilage forming tumours
• Benign: - Osteochondroma (exostosis)
- Enchondroma (chondroma)
- Chondromyxoid fibroma
- Chondroblastoma
• Malignant: - Chondrosarcoma
Giant cell tumours (GCT)
• Benign/ Indeterminate /Malignant
Marrow tumours
• ES/MM/Lymphoma
Vascular tumours
• Benign: - Haemangioma/
• Malignant: - Angiosarcoma
GCT
GCT(OC)
• Aggressive tumours
• Benign,
• Pulmonary mets in 3% (spontaneous
regression/ asymptomatic)
• Primary
• Secondary- previous rad therapy
GCT(OC)
M/C location; epiphysis of
Long bone
• Distal femur
• Prox. Tibia
• Distal radius
C/F
• 20-40yrs age
• F>M
• swelling
• Progressive pain
• Severe- pathological #
• Soft tissue extension
• EGG SHELL CRACKELING
X- ray features
• Eccentric
• Purely lytic
• Poorly defined zone of transition
• ± cortical breach
• SOAP BUBBLE APPEARANCE
• Never goes into joint, abuts subchondral bone
DIAGNOSIS
• History
• Physical examination
• X- ray
• MRI- soft tissue extent
- F/F level(secondary ABC)
• Biopsy- confirmatory
HISTOPATHOLOGY
• Multinucleated giant cells(40-60 nuclei/cell)
• Mononuclear stromal cells
• IDENTICAL NUCLEI
• ± Secondary ABC cells
TREATMENT
• Simple curettage- recurrance 50%
• Extended curettage – recurrance 5-15%
- liq. Nitrogen
- argon beam coagulation
- phenol
- electrocautery
- bone cement
POST CURETTAGE-DEFECT FILLING
BONE CEMENT
• Easier detection of
tumour recurrance
• Quicker
rehabilitation
• PMMA
BONE GRAFT
• Recurrance is
difficult to
distinguish
• Risk of pathological
#, joint must be
protected . Late
rehab
TREATMENT -GCT
• Excision- ulna, fibula
• Excision and reconstruction- distal femur,
- prox tibia
• Arthrodesis by the Turn-o-Plasty procedure
• Arthrodesis by bridging the gap by double
fibulae
• Arthroplasty
Arthrodesis by the Turn-o-Plasty
procedure
• For distal femur GCT
• Length of the tibia is split into two halves.
• One half is turned upside down
• Fixed with the stump of the femur left after
excising the tumour.
• Same for proximal tibia GCT
• By taking half of femur
Arthrodesis by bridging the gap by
double
fibulae
• one taken from same extremity
• the other from the opposite leg
Arthroplasty:
• Tumour is excised
• Attempt is made to reconstruct the joint in
some way
• Painless, mobile joint achieved
TREATMENT-GCT
• EMBOLISATION- spine, pelvic GCT
• RESECTION- pulm. mets
THANK YOU

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Introduction to bone tumours and GCT

  • 1. INTRODUCTION TO BONE TUMOURS AND GCT Dr. Lokesh Chugh PG resident GMC. Amritsar.
  • 2. INTRODUCTION • Bony lesions • Arises from bone itself (primary) • Arrived from distant sites (secondary) • Benign • Malignant
  • 3. DIAGNOSTIC EVALUATION • Adequate history, C/F • Physical examination • Radiological examination-benign vs malignant • Biopsy- confirmatory
  • 4. • pain, mass • Surrounding muscle atropy – disuse of limb • Neurological deficit- nerve involvement • Café-au-lait spot- NF • Lymph node metastasis- synovial sarcoma
  • 5. MASS • Consistency • Mobility • Tenderness • Local temperature
  • 6. • Dimensions • Location • Shape • Change with position
  • 8. EPIPHYSEAL LESIONS - D/D • Chondroblastoma (10-25yrs)- central, can cross joint line (benign) • GCT (20-40 yrs)- eccentric, soap bubble appaerance, never crosses joint line (locally aggressive) • Clear chondrosarcoma (rare) (malignant)
  • 9. DIAPHYSEAL LESIONS – D/D • EWING SARCOMA (5-25 yrs) (Onion peel ) • LYMPHOMA (ADULTS) • FIBROUS DYSPLASIA (5-30yrs) (Shepherd crook deformity) • HISTIOCYTOSIS(5-30yrs)
  • 10. SPINE LESIONS –D/D ≥40 yrs • Metastasis • MM • Cordoma ≤ 30 yrs • OO • OB • ABC
  • 11. MULTIPLE LESIONS - D/D • MM • METASTASIS • FD • HEMANGIOMA • INFECTION • HYPERPTH
  • 12. BENIGN VS MALIGNANT • Low biological activity, ± surrounded by rim of reactive bone • Well marginated • Narrow zone of transition(long standing, non aggresive) • Geographical pattern of osteolytic destruction • High biological activity, shows periosteal rxn • Poorly marginated • wide defined zone of transition (fast growing, aggressive) • Non geographical/ poorly defined cortical destruction
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  • 14. PERIOSTEAL REACTION • New bone formation • When tumour destroys the cortex • CODMAN TRIANGLE -OS • ONION SKINNING -ES • SUN BURST APPEARANCE -OS • D/D- malignancy, infection, histiocytosis
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  • 18. BONE MATRIX • Calcific stippling- enchondroma, CS • Matrix ossification- OS • Ground glass app.- FD
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  • 23. Bone forming tumours • Benign: - Osteoid osteoma, osteoma - Osteoblastoma • Indeterminate - Aggressive osteoblastoma • Malignant - Osteosarcoma conventional, variants
  • 24. Cartilage forming tumours • Benign: - Osteochondroma (exostosis) - Enchondroma (chondroma) - Chondromyxoid fibroma - Chondroblastoma • Malignant: - Chondrosarcoma
  • 25. Giant cell tumours (GCT) • Benign/ Indeterminate /Malignant Marrow tumours • ES/MM/Lymphoma Vascular tumours • Benign: - Haemangioma/ • Malignant: - Angiosarcoma
  • 26. GCT
  • 27. GCT(OC) • Aggressive tumours • Benign, • Pulmonary mets in 3% (spontaneous regression/ asymptomatic) • Primary • Secondary- previous rad therapy
  • 28. GCT(OC) M/C location; epiphysis of Long bone • Distal femur • Prox. Tibia • Distal radius
  • 29. C/F • 20-40yrs age • F>M • swelling • Progressive pain • Severe- pathological # • Soft tissue extension • EGG SHELL CRACKELING
  • 30. X- ray features • Eccentric • Purely lytic • Poorly defined zone of transition • ± cortical breach • SOAP BUBBLE APPEARANCE • Never goes into joint, abuts subchondral bone
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  • 34. DIAGNOSIS • History • Physical examination • X- ray • MRI- soft tissue extent - F/F level(secondary ABC) • Biopsy- confirmatory
  • 35. HISTOPATHOLOGY • Multinucleated giant cells(40-60 nuclei/cell) • Mononuclear stromal cells • IDENTICAL NUCLEI • ± Secondary ABC cells
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  • 37. TREATMENT • Simple curettage- recurrance 50% • Extended curettage – recurrance 5-15% - liq. Nitrogen - argon beam coagulation - phenol - electrocautery - bone cement
  • 38. POST CURETTAGE-DEFECT FILLING BONE CEMENT • Easier detection of tumour recurrance • Quicker rehabilitation • PMMA BONE GRAFT • Recurrance is difficult to distinguish • Risk of pathological #, joint must be protected . Late rehab
  • 39. TREATMENT -GCT • Excision- ulna, fibula • Excision and reconstruction- distal femur, - prox tibia • Arthrodesis by the Turn-o-Plasty procedure • Arthrodesis by bridging the gap by double fibulae • Arthroplasty
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  • 41. Arthrodesis by the Turn-o-Plasty procedure • For distal femur GCT • Length of the tibia is split into two halves. • One half is turned upside down • Fixed with the stump of the femur left after excising the tumour. • Same for proximal tibia GCT • By taking half of femur
  • 42. Arthrodesis by bridging the gap by double fibulae • one taken from same extremity • the other from the opposite leg
  • 43. Arthroplasty: • Tumour is excised • Attempt is made to reconstruct the joint in some way • Painless, mobile joint achieved
  • 44. TREATMENT-GCT • EMBOLISATION- spine, pelvic GCT • RESECTION- pulm. mets