Site :
Metaphysis of the lower end of the femur, the upper end of the tibia and
humors.
Age incidence
-
10-25 years (prior to epiphyseal fusion)
-
Old age (Secondary to paget’s disease)
Sex- Boys > Girls
The tumour extends within
the medulla and across the physeal plate and extending into the soft tissue.
Grey white invasive and destructive masses having focal haemorrhase &
nerosis. There are areas of bone loss and cavitation alternate with dense
patches of abnormal new bone.
Clinical Features
Ø Pain, swelling, near a joint
with history of trauma
Ø Overlying skin stretched
& shiny
Ø Local rise of temp due to
increased vascularily
Ø Firm in consistency
Ø Sign & symptoms of
bronchitis, pnenmonia if there is lung metastasis
Ø Pathological fracture
Spread- haematogenous spread to lung, usually sometimes to other bone.
Types:
a) Primary or Secondary
b) Dahlin’s prognostic
classification
Ø Osteoblastic
Ø Chondroblastic
Ø Fibroblastic
c) Geschickter and copeland
classification
Ø Selerosing type
Ø Osteolytic type
Ø Both osteoblastic and
osteolytic (Mixed)
Ø Telangicetatic.
X-ray
1. Both osteolytic (Radiolucent) & osteolbastic (Dense) areas
2. Sunray appearance – due to deposition of tumour osteoid along the
vessels.
3. Codman’s triangle- due to raised periosteum
CT & MRI: To see extend of the tumour
X-ray Chest: To see pulmonary metastasis.
Biopsy
1. FNAC
2. Open biopsy
Varients of osteosarcoma
Parosteal : A thin gap between cortex & tumour, cortex is not corded.
Periosteal : A
superficial defect of the cortex
Paget’s
sarcoma : Feature’s of paget’s disease + Bone destruction with soft tissue
invasion.
Treatment
·
Multi-agent chemotherapy for 8-12 weeks
·
Resection of the tumour or amputation
·
The pathological specimen is examined to assess the response to
preoperative chemotherapy. It tumour necrosis is marked, chemotherapy is
continued for another 6-12 months.
·
Bone gap is filled by a large bone graft and custom-made implant.
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