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፠ Osteosarcoma is the third most common cancer in
adolescence .
፠ Occurring less frequency than only lymphomas and brain
tumors.
፠ It is thought to arise from a primitive mesenchymal bone
forming cell and is characterized by production of osteoid.
Conventional osteosarcoma is a
primary intramedullary high grade malignant tumour in
which the neoplastic cells produce osteoid, even if only in
small amounts.
WHO 2002
፠ Conventional osteosarcoma.
፠ Classical osteosarcoma.
፠ Osteogenic sarcoma.
፠ Osteosarcoma not otherwise specified.
፠ Osteochondrosarcoma, osteoblastic sarcoma.
፠ Chondroblastic osteosarcoma.
፠ Fibroblastic osteosarcoma.
፠ Osteofibrosarcoma.
፠ Central osteosarcoma.
፠ Central osteogenic sarcoma.
፠ Conventional central osteosarcoma.
፠ Medullary osteosarcoma.
፠ Sclerosing osteosarcoma.
• Occurs chiefly in young individuals (10-25 years).
• More dramatic increase in adolescence corresponds
with growth spurt
AGE
• Incidence is slightly higher in males than in females
(1.25:1)
GENDER
• Most commonly occurs in long bones of the extremities
near mataphyseal growth plate.
• Femur(42%), tibia (19%), humerus(10%). Other significant
location are skull or jaw (8%) and pelvis (8%).
LOCATION
Rapid Bone
Growth
Increase incidence
during adolescent
growth spurts
Location near
metaphyseal growth
plates of long bone
Genetic
Deletion of
13q14 (Familial
Retinoblastoma)
Le Fraumeni
Syndrome
(Germline
TP53
mutation)
Rothmund
Thomson
Syndrome
Bone
Dysplasia
Paget’s Disease Fibrous Dysplasia
Other
factors
• Bone infarcts.
• Chronic osteomyelitis,
• Trauma.
• Viral infection.
• Exposure to high-dose radiation
፠ Swelling and pain are the early
features of neoplasm.
፠ Patient may complain of sprain,
arthritis or grawing pain.
፠ Oral manifestation includes
swelling of involved area, facial
deformity and pain, loose teeth,
paresthesia, toothache, bleeding,
nasal obstruction.
፠ Radiographic appearance is
variable depending upon on the
amount of tumor bone
synthesised by malignant
osteoblast.
Tumors with little tumor bone- Radiolucent
Intermediate degree of bone - Mixed lucent-dense lesions
Tumors with much more tumor bone- Radiodense
In jaw bones= Lytic pattern> sclerotic > mixed pattern
Sunray / Sunburst
Appearances
Cumulus Cloud
Densities
Codmans Triangle
፠ Uniform widening of pdl space
that may be associated with
loss of lamina dura and is
important radiographic
feature.
Advance Imaging Technique
፠ Histopathologically osteosarcoma is defined as tumor
characterized by the direct formation of osteoid or
primitive woven bone by malignant tumor stromal
cells.
OSTEOSARCOMA
CONVENTIONAL
TELENGIECTATIC
SMALL CELL
LOW GRADE CENTRAL
OSTEOSARCOMA
PERIOSTEAL &
PARAOSTEAL
HIGH GRADE SURFACE
SECONDARY
OSTEOSARCOMA
EXTRAOSSEOUS
Osteoblastic (50%)
Chondroblastic (25%)
Fibroblastic (25%)
Chondroblastoma like
Osteosarcoma
Osteoblastoma Like
Osteosarcoma
MFH like Osteosarcoma
Giant Cell Rich Osteosarcoma
Epithelioid Osteosarcoma
፠ Osteosarcoma is usually large (>5
cm) fleshy or hard tumor
፠ Tumor appearance an consistency
varies considerably depending
upon the proportion of cartilage,
fibrous tissue and bone present.
፠ It may be pink-gray white with
fishs flesh appearance to gray-
blue gray with firm white fibrous
nodular mass.
፠ In tumor with abundant bone
formation it may be too hard and
requires saw to section.
፠ Bone and/or osteoid are the predominant matrix in osteoblastic
osteosarcoma.
፠ Finding of greater proportion of unequivocal osteoid or tumor
bone formed by malignant appearing stromal cells suggest the
diagnosis of osteoblastic osteosarcoma.
፠ Infiltrative pattern .
፠ Atypical pleomorphic stroma cells.
፠ Atypical mitotic figures.
፠ Areas of necrosis and malignant cartilagenous area.
Aggressive
Osteoblastoma
፠ Chondroblastic osteosarcomas contain an abundance of
malignant appearing chondroid and cartilage, arranged in
lobules or islands, with cells within lacunar spaces.
፠ Identification of foci of malignant osteoid formation
Chondrosarcoma
፠ Contains large areas composed of spindle cells that may assume
a herringbone pattern along with malignant tumor cells with
formation of tumor osteoid.
Fibrosarcoma
፠ Herringbone pattern
፠ IHC
A malignant bone-forming tumour
characterized by large spaces filled with
blood with or without septa. The
roentgenogram typically shows a purely lytic
destructive process without matrix
mineralisation.
፠ Etiology is unknown, few cases been
associated with Paget’s disease.
፠ Clinical presentation is same as that of
conventional osteosarcoma with
characteristic pathological fracture of bone.
WHO 2002
፠ The tumour contains blood-filled or empty spaces separated by
thin septa.
፠ The septa are cellular, containing highly haemorrhagic area.
፠ Cellular septe contain many benign looking multinucleated giant
cells.
፠ Significant anaplasia of cells within cyst walls
፠ Conspicuous mitoses,
፠ Atypical mitotic figures
፠ Subtle, focal osteoid deposition
፠ Tumoral necrosis
Aneurysmal
Bone Cyst
፠ Ostesarcoma do not have any specific markers.
፠ Wide panel of markers can be applied:
1. Osteonectin.
2. Osteocalcin.
3. Cytokeratin.
4. S100.
5. Ki-67.
6. P53.
7. CD99.
Ki 67
p53
፠ Radical resection is choice of t/t yielding best prognosis.
፠ Intralesional or marginal excision leads to local resection & carry
poor prognosis.
፠ Rate of local recurrence in max Osteosarcoma is 29-60% & in
mandibular lesion from 43-66%
፠ Metastasis from mandibular tumors are more frequent than
maxillary tumors.
፠ Overall 5 yr survival rate after radical excision for max OS=
25-63% & for mandibular OS= 24-71%.
፠ Mandibular lesion have better prognosis than maxillary lesions.
osteosarcoma.ppt
osteosarcoma.ppt

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osteosarcoma.ppt

  • 1.
  • 2. ፠ Osteosarcoma is the third most common cancer in adolescence . ፠ Occurring less frequency than only lymphomas and brain tumors. ፠ It is thought to arise from a primitive mesenchymal bone forming cell and is characterized by production of osteoid.
  • 3. Conventional osteosarcoma is a primary intramedullary high grade malignant tumour in which the neoplastic cells produce osteoid, even if only in small amounts. WHO 2002
  • 4. ፠ Conventional osteosarcoma. ፠ Classical osteosarcoma. ፠ Osteogenic sarcoma. ፠ Osteosarcoma not otherwise specified. ፠ Osteochondrosarcoma, osteoblastic sarcoma. ፠ Chondroblastic osteosarcoma. ፠ Fibroblastic osteosarcoma. ፠ Osteofibrosarcoma. ፠ Central osteosarcoma. ፠ Central osteogenic sarcoma. ፠ Conventional central osteosarcoma. ፠ Medullary osteosarcoma. ፠ Sclerosing osteosarcoma.
  • 5. • Occurs chiefly in young individuals (10-25 years). • More dramatic increase in adolescence corresponds with growth spurt AGE • Incidence is slightly higher in males than in females (1.25:1) GENDER • Most commonly occurs in long bones of the extremities near mataphyseal growth plate. • Femur(42%), tibia (19%), humerus(10%). Other significant location are skull or jaw (8%) and pelvis (8%). LOCATION
  • 6. Rapid Bone Growth Increase incidence during adolescent growth spurts Location near metaphyseal growth plates of long bone Genetic Deletion of 13q14 (Familial Retinoblastoma) Le Fraumeni Syndrome (Germline TP53 mutation) Rothmund Thomson Syndrome Bone Dysplasia Paget’s Disease Fibrous Dysplasia
  • 7. Other factors • Bone infarcts. • Chronic osteomyelitis, • Trauma. • Viral infection. • Exposure to high-dose radiation
  • 8. ፠ Swelling and pain are the early features of neoplasm. ፠ Patient may complain of sprain, arthritis or grawing pain. ፠ Oral manifestation includes swelling of involved area, facial deformity and pain, loose teeth, paresthesia, toothache, bleeding, nasal obstruction.
  • 9. ፠ Radiographic appearance is variable depending upon on the amount of tumor bone synthesised by malignant osteoblast. Tumors with little tumor bone- Radiolucent Intermediate degree of bone - Mixed lucent-dense lesions Tumors with much more tumor bone- Radiodense In jaw bones= Lytic pattern> sclerotic > mixed pattern
  • 13. ፠ Uniform widening of pdl space that may be associated with loss of lamina dura and is important radiographic feature.
  • 15. ፠ Histopathologically osteosarcoma is defined as tumor characterized by the direct formation of osteoid or primitive woven bone by malignant tumor stromal cells.
  • 16. OSTEOSARCOMA CONVENTIONAL TELENGIECTATIC SMALL CELL LOW GRADE CENTRAL OSTEOSARCOMA PERIOSTEAL & PARAOSTEAL HIGH GRADE SURFACE SECONDARY OSTEOSARCOMA EXTRAOSSEOUS
  • 17. Osteoblastic (50%) Chondroblastic (25%) Fibroblastic (25%) Chondroblastoma like Osteosarcoma Osteoblastoma Like Osteosarcoma MFH like Osteosarcoma Giant Cell Rich Osteosarcoma Epithelioid Osteosarcoma
  • 18. ፠ Osteosarcoma is usually large (>5 cm) fleshy or hard tumor ፠ Tumor appearance an consistency varies considerably depending upon the proportion of cartilage, fibrous tissue and bone present. ፠ It may be pink-gray white with fishs flesh appearance to gray- blue gray with firm white fibrous nodular mass. ፠ In tumor with abundant bone formation it may be too hard and requires saw to section.
  • 19. ፠ Bone and/or osteoid are the predominant matrix in osteoblastic osteosarcoma. ፠ Finding of greater proportion of unequivocal osteoid or tumor bone formed by malignant appearing stromal cells suggest the diagnosis of osteoblastic osteosarcoma.
  • 20. ፠ Infiltrative pattern . ፠ Atypical pleomorphic stroma cells. ፠ Atypical mitotic figures. ፠ Areas of necrosis and malignant cartilagenous area. Aggressive Osteoblastoma
  • 21. ፠ Chondroblastic osteosarcomas contain an abundance of malignant appearing chondroid and cartilage, arranged in lobules or islands, with cells within lacunar spaces.
  • 22. ፠ Identification of foci of malignant osteoid formation Chondrosarcoma
  • 23. ፠ Contains large areas composed of spindle cells that may assume a herringbone pattern along with malignant tumor cells with formation of tumor osteoid.
  • 25. A malignant bone-forming tumour characterized by large spaces filled with blood with or without septa. The roentgenogram typically shows a purely lytic destructive process without matrix mineralisation. ፠ Etiology is unknown, few cases been associated with Paget’s disease. ፠ Clinical presentation is same as that of conventional osteosarcoma with characteristic pathological fracture of bone. WHO 2002
  • 26. ፠ The tumour contains blood-filled or empty spaces separated by thin septa. ፠ The septa are cellular, containing highly haemorrhagic area. ፠ Cellular septe contain many benign looking multinucleated giant cells.
  • 27. ፠ Significant anaplasia of cells within cyst walls ፠ Conspicuous mitoses, ፠ Atypical mitotic figures ፠ Subtle, focal osteoid deposition ፠ Tumoral necrosis Aneurysmal Bone Cyst
  • 28. ፠ Ostesarcoma do not have any specific markers. ፠ Wide panel of markers can be applied: 1. Osteonectin. 2. Osteocalcin. 3. Cytokeratin. 4. S100. 5. Ki-67. 6. P53. 7. CD99. Ki 67 p53
  • 29. ፠ Radical resection is choice of t/t yielding best prognosis. ፠ Intralesional or marginal excision leads to local resection & carry poor prognosis. ፠ Rate of local recurrence in max Osteosarcoma is 29-60% & in mandibular lesion from 43-66% ፠ Metastasis from mandibular tumors are more frequent than maxillary tumors.
  • 30. ፠ Overall 5 yr survival rate after radical excision for max OS= 25-63% & for mandibular OS= 24-71%. ፠ Mandibular lesion have better prognosis than maxillary lesions.

Editor's Notes

  1. Radiograph showing dense sclerotic change in bone.
  2. Computed tomography scan shows involvement of the right side of the mandible with a sunburst appearance.
  3. 2 Osteosarcoma presenting as mixed lytic / blastic lesion involving the distal femoral metaphysis of a skeletally immature patient. The radiodensity pattern is "cumulus cloud-like". 1 pelvis osteosarcoma showing lobulated mixed lucent dense area called as cumulus cloud
  4. In long bone, periostium is elevated over the surface of expanding tumor mass in a tent like fashion. At the point where periosteium begins to merge(edge to tent) an acute angle between periosteium and bone surface is created called as codmans triangle. Codman’s reactive triangle is frequently found in osteosarcoma of bone; however, it is not pathognomonic of osteosarcoma and can be found in infectious lesions, traumatic periostitis, and peculiar callus formations. Note the mixed pattern of osteosarcoma in the proximal metaphysis of the tibia.
  5. Radiograph showing dense sclerotic change in bone.
  6. CT scan showed mixed sclerotic mass involving the right maxillaand nasal cavity with involvement of infraorbital floor,nasal cavity, frontal, sphenoidal, and ethemoidal sinuses and was reported as osteoma of maxilla
  7. Aneurysmal bone cyst with reactive granulation-like tissue, metaplastic ossification with osteoblastic rimming, and osteoclast-like giant cells within cyst walls