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Giant Cell Tumor of Bone
Definition
• 10 bone neoplasm
• First described Cooper 1818
• Generally benign but locally aggressive
• Potential for :
– Recurrence
– Pulmonary metastasis
– Frank malignancy
• Osteolytic tumour arising from
epiphysis
• Common in young adults
• Though it is benign it is locally
malignant
Epidemiology
• 5-10% 10 bone tumors
• 20% benign bone tumors
• F : M 1.5 : 1
• 70-80% age 20-40yrs
SITES
• Most common location –distal femur followed
closely by the proximal tibia
• In the distal radius(3rd most common location)
these are frequently more aggressive
Presentation
• Swelling with skin over the
swelling stretched
• Pain x wks. – mos(usually not a presenting
feature
• Mass
• Pathologic #
• Neuro deficit (spine / sacrum)
• Incidental
• EGG SHELL CRACKING sensation may be
present
• Limitation of joint movement and pathological
fractures –usually a late feature
Radiology
• Lytic lesion near epiphysis
• Eccentric or central
• Narrow zone transition B/W
tmr and surrounding tissue
• Cortical thinning
• expansile
• No sclerotic margin
• No periosteal bone formation
• Thin septa of bone traverse the interior
producing soap bubble appearance
• Joint extension usually not a feature
• Cortex disrupted in late stages
• Intra articular extension is rare as subchondral
bone usually remains intact
Other modalities
• CT
– Integrity cortical rim
• MRI
_extent of lesion within the bone and soft tissue
– Assess subchondral breakthrough
– Lesion dark on T1 and bright on T2 wt
• Bone Scan
– Suspect multicentri loci
– Uses very low radioactive material
(disphosphonate) to see spread to other bone
CAMPANACCI’S GRADING
• GRADE 1 :CYSTIC LESION
• GRADE 2:CORTEX THIN BUT NOT PERFORATED
• GRADE 3:CORTEX PERFORATED WITH
EXTENSION INTO SOFT TISSUE
ENEKING’S STAGING
• STAGE 1: LATENT-NO CHARACTERISTIC
GROWTH OR PROGRESSIVE CHANGE,RESOLVE
SPONTANEOUSLY
• STAGE 2:ACTIVE-LESION DEFORM THE HOST
BONE BUT REMAINS INSIDE BONE
• STAGE3:AGGRESSIVE-TUMOUR EXTEND
BEYOND THE BONE
Histology
• Fibrohistiocytic origin
• Multinucleated giant cells
(40-60 nuclei per cell) in a sea
of mononuclear stroma
– Round / ovoid / spindle
• Indistinct cell membrane
• Mitoses
• Appearance of spindle cells-malignant
potential
• GCT USUALLY ARE SOLITARY
LESIONS;HOWEVER 1%-2% MAY BE
SYNCHRONOUSLY OR METACHRONOUSLY
MULTICENTRIC
PULMONARY METASTASIS
• OVERALL MORTALITY:15%
• PATIENT WITH RECURRENT LESIONS OR
PRIMARY LESIONS THAT APPEAR AGGRESSIVE
RADIOGRAPHICALLY ARE AT HIGHER RISK
• MALIGNANT GCT <5% CASES
TREATMENT
• Traditionally:
– Intralesional curettage / resection & bone graft
– Recurrence 35-42%
• En Bloc resection
– Recurrence ~10%
– Multiple complications
• Adjuvant
• HISTORICALLY TRT CONSISTED OF SIMPLE CURETTAGE
• BUT RECURRENCE RATES > 50%
• FOR DEFECTS AFTER RESECTION OR
CURETTAGE,EITHER ALLOGRAFT OR BONE CEMENT
USED AS FILLING AGENTS
EXTENDED CURETTAGE –USE OF A POWER BURR TO
ENLARGE THE CAVITY 1-2 CM IN ALL DIRECTIONS IS
NOW CONSIDERED STANDARD
Curettings
Adjuvant Tx
• PMMA, Liquid N2, Phenol, CO2 laser,
Electrocautery
– Local extension of margin
– Kill residual foci and remaining tumour cell
• ASSOCIATED WITH PATHOLOGIC
FRACTURES,WOUND HEALING PROBLEMS
BONE GRAFT
ADVANTAGE:
• RESTORING NORMAL BIOMECHANICS TO
JOINT SURFACE
• PREVENT FUTURE DEGENERATIVE JOINT
DISEASES
• RESTORING BONE STOCK
• DISADVANTAGES
JOINT MUST BE PROTECTED FOR AN
EXTENDED PERIOD OF TIME TO PREVENT A
PATHOLOGICAL FRACTURES
TUMOUR RECURRENCE IS DIFFICULT TO
DISTINGUISH FROM GRAFT RESORPTION
• THE ABOVE DISADVANTAGES OVERCOME BY
USE OF BONE CEMENT
• PROVIDES IMMEDIATE STABILITY-HENCE
QUICKER REHABILITATION
• EASIER DETECTION OF RECURRENCE SEEN AS
EXPANDING RADIOLUCENCY ADJ TO CEMENT
• KILLS RESIDUAL TMR CELLS
THRUPOLYMERISATION
Enbloc Resection
• Expendable bones
– Prox fibula / Distal ulna
• Eroded cortex and extended into
soft tissue
• Recurrence
• Pathologic #
• Joint involvement
• INITIAL PROCEDURE OF CHOICE AND HERE
2CM OF NORMAL BONE IS ALSO EXCISED
• DEFECTS ARE FILLED WITH CANCELLOUS BONE
GRAFTS,FREEZE DRIED ALLOGRAFT OR
PROSTHESIS
• AROUND THE KNEE,A HEMICONDYLAR
OSTEOARTICULAR ALLOGRAFT
RECONSTUCTION OR A ROTATING HINGE
ENDOPROSTHESIS MAY BE NECESSARY
• FOR AGGRESSIVE LESION OF DISTAL
RADIUS,PRIMARY RESECTION AND
RECONSTRUCTION WITH A PROXIMAL
FIBULAR AUTOGRAFT INDICATED
• FOR LESIONS IN EXPENDABLE BONES(DISTAL
ULNA OR PROXIMAL FIBULA)PRIMARY
RESECTION WITHOUT RECONSTRUCTION
INDICATED
• FOR INOPERABLE LESIONS IN SPINE OR
PELVIS,RADIATION MAY BE USED
EXCISION AND RECONSTRUCTION
• FOR GCT AFFECTING LOWER END OF
FEMUROR UPPER END OF TIBIA
• AFTER EN BLOCK EXCISION RECONSTRUCTION
CAN BE DONE BY
1.TURN-O-PLASTY TECHNIQUE
2.ARTHRODESIS
3.ARTHROPLASTY
RECURRENCE OF LESIONS
• MOST LOCAL RECURRENCES AND
PULMONARY METASTASES OCCUR WITHIN
3YRS OR EVEN UPTO 20 YRS
• PATIENT SHOULD HAVE RADIOGRAPH OF THE
PRIMARY TUMOUR SITE AND THE CHEST AT
3MONTHS INTERVAL FOR 1YR
6MONTHS INTERVAL FOR NEXT 2 YRS
AND ANNUALLY THEREAFTER
• TREATMENT IS SAME AS FOR PRIMARY
LESIONS.
• AFTER BIOPSY SHOWS THAT TUMOUR IS STILL
BENIGN,REPEAT CURETTAGE OR RESECTION IS
PERFORMED
THANK YOU

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Giant cell tumor of bone

  • 2. Definition • 10 bone neoplasm • First described Cooper 1818 • Generally benign but locally aggressive • Potential for : – Recurrence – Pulmonary metastasis – Frank malignancy
  • 3. • Osteolytic tumour arising from epiphysis • Common in young adults • Though it is benign it is locally malignant
  • 4. Epidemiology • 5-10% 10 bone tumors • 20% benign bone tumors • F : M 1.5 : 1 • 70-80% age 20-40yrs
  • 5. SITES • Most common location –distal femur followed closely by the proximal tibia • In the distal radius(3rd most common location) these are frequently more aggressive
  • 6. Presentation • Swelling with skin over the swelling stretched • Pain x wks. – mos(usually not a presenting feature • Mass • Pathologic # • Neuro deficit (spine / sacrum) • Incidental
  • 7. • EGG SHELL CRACKING sensation may be present • Limitation of joint movement and pathological fractures –usually a late feature
  • 8. Radiology • Lytic lesion near epiphysis • Eccentric or central • Narrow zone transition B/W tmr and surrounding tissue • Cortical thinning • expansile • No sclerotic margin • No periosteal bone formation
  • 9. • Thin septa of bone traverse the interior producing soap bubble appearance • Joint extension usually not a feature • Cortex disrupted in late stages • Intra articular extension is rare as subchondral bone usually remains intact
  • 10.
  • 11.
  • 12.
  • 13. Other modalities • CT – Integrity cortical rim • MRI _extent of lesion within the bone and soft tissue – Assess subchondral breakthrough – Lesion dark on T1 and bright on T2 wt • Bone Scan – Suspect multicentri loci – Uses very low radioactive material (disphosphonate) to see spread to other bone
  • 14.
  • 15. CAMPANACCI’S GRADING • GRADE 1 :CYSTIC LESION • GRADE 2:CORTEX THIN BUT NOT PERFORATED • GRADE 3:CORTEX PERFORATED WITH EXTENSION INTO SOFT TISSUE
  • 16. ENEKING’S STAGING • STAGE 1: LATENT-NO CHARACTERISTIC GROWTH OR PROGRESSIVE CHANGE,RESOLVE SPONTANEOUSLY • STAGE 2:ACTIVE-LESION DEFORM THE HOST BONE BUT REMAINS INSIDE BONE • STAGE3:AGGRESSIVE-TUMOUR EXTEND BEYOND THE BONE
  • 17. Histology • Fibrohistiocytic origin • Multinucleated giant cells (40-60 nuclei per cell) in a sea of mononuclear stroma – Round / ovoid / spindle • Indistinct cell membrane • Mitoses • Appearance of spindle cells-malignant potential
  • 18. • GCT USUALLY ARE SOLITARY LESIONS;HOWEVER 1%-2% MAY BE SYNCHRONOUSLY OR METACHRONOUSLY MULTICENTRIC
  • 19.
  • 20. PULMONARY METASTASIS • OVERALL MORTALITY:15% • PATIENT WITH RECURRENT LESIONS OR PRIMARY LESIONS THAT APPEAR AGGRESSIVE RADIOGRAPHICALLY ARE AT HIGHER RISK • MALIGNANT GCT <5% CASES
  • 21. TREATMENT • Traditionally: – Intralesional curettage / resection & bone graft – Recurrence 35-42% • En Bloc resection – Recurrence ~10% – Multiple complications • Adjuvant
  • 22. • HISTORICALLY TRT CONSISTED OF SIMPLE CURETTAGE • BUT RECURRENCE RATES > 50% • FOR DEFECTS AFTER RESECTION OR CURETTAGE,EITHER ALLOGRAFT OR BONE CEMENT USED AS FILLING AGENTS EXTENDED CURETTAGE –USE OF A POWER BURR TO ENLARGE THE CAVITY 1-2 CM IN ALL DIRECTIONS IS NOW CONSIDERED STANDARD
  • 24. Adjuvant Tx • PMMA, Liquid N2, Phenol, CO2 laser, Electrocautery – Local extension of margin – Kill residual foci and remaining tumour cell • ASSOCIATED WITH PATHOLOGIC FRACTURES,WOUND HEALING PROBLEMS
  • 25. BONE GRAFT ADVANTAGE: • RESTORING NORMAL BIOMECHANICS TO JOINT SURFACE • PREVENT FUTURE DEGENERATIVE JOINT DISEASES • RESTORING BONE STOCK
  • 26. • DISADVANTAGES JOINT MUST BE PROTECTED FOR AN EXTENDED PERIOD OF TIME TO PREVENT A PATHOLOGICAL FRACTURES TUMOUR RECURRENCE IS DIFFICULT TO DISTINGUISH FROM GRAFT RESORPTION
  • 27. • THE ABOVE DISADVANTAGES OVERCOME BY USE OF BONE CEMENT • PROVIDES IMMEDIATE STABILITY-HENCE QUICKER REHABILITATION • EASIER DETECTION OF RECURRENCE SEEN AS EXPANDING RADIOLUCENCY ADJ TO CEMENT • KILLS RESIDUAL TMR CELLS THRUPOLYMERISATION
  • 28. Enbloc Resection • Expendable bones – Prox fibula / Distal ulna • Eroded cortex and extended into soft tissue • Recurrence • Pathologic # • Joint involvement
  • 29. • INITIAL PROCEDURE OF CHOICE AND HERE 2CM OF NORMAL BONE IS ALSO EXCISED • DEFECTS ARE FILLED WITH CANCELLOUS BONE GRAFTS,FREEZE DRIED ALLOGRAFT OR PROSTHESIS
  • 30. • AROUND THE KNEE,A HEMICONDYLAR OSTEOARTICULAR ALLOGRAFT RECONSTUCTION OR A ROTATING HINGE ENDOPROSTHESIS MAY BE NECESSARY • FOR AGGRESSIVE LESION OF DISTAL RADIUS,PRIMARY RESECTION AND RECONSTRUCTION WITH A PROXIMAL FIBULAR AUTOGRAFT INDICATED
  • 31. • FOR LESIONS IN EXPENDABLE BONES(DISTAL ULNA OR PROXIMAL FIBULA)PRIMARY RESECTION WITHOUT RECONSTRUCTION INDICATED • FOR INOPERABLE LESIONS IN SPINE OR PELVIS,RADIATION MAY BE USED
  • 32.
  • 33. EXCISION AND RECONSTRUCTION • FOR GCT AFFECTING LOWER END OF FEMUROR UPPER END OF TIBIA • AFTER EN BLOCK EXCISION RECONSTRUCTION CAN BE DONE BY 1.TURN-O-PLASTY TECHNIQUE 2.ARTHRODESIS 3.ARTHROPLASTY
  • 34. RECURRENCE OF LESIONS • MOST LOCAL RECURRENCES AND PULMONARY METASTASES OCCUR WITHIN 3YRS OR EVEN UPTO 20 YRS • PATIENT SHOULD HAVE RADIOGRAPH OF THE PRIMARY TUMOUR SITE AND THE CHEST AT 3MONTHS INTERVAL FOR 1YR 6MONTHS INTERVAL FOR NEXT 2 YRS AND ANNUALLY THEREAFTER
  • 35. • TREATMENT IS SAME AS FOR PRIMARY LESIONS. • AFTER BIOPSY SHOWS THAT TUMOUR IS STILL BENIGN,REPEAT CURETTAGE OR RESECTION IS PERFORMED