The term bone tumor is a broad term used for benign and malignant neoplasm.
metastatic deposits in the bone are common than the primary bone tumors.
most primary bone tumors occur in children and young adult.
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Bone Tumor.pptx
1.
2. INTRODUCTION
•The term bone tumor is a broad term used for
benign and malignant neoplasm.
• metastatic deposits in the bone are common than
the primary bone tumors.
• most primary bone tumors occur in children and
young adult.
4. Osteoma
•It is a benign tumor composed of sclerotic, well formed bone
protruding from cortical surface of a bone.
• The bone involved most often are the skull and facial.
• Generally, the tumor has no clinical significance except that it may
produce visible swelling.
• Sometimes it may bulge into the air sinuses and cause obstruction to
the sinus cavity, and leading to pain.
5. Treatment
•No treatment is generally required except for cosmetic reasons.
• Simple excision is sufficient.
6. Osteoid osteoma
•It is the most commonest true benign tumor of the bone.
• Pathologically, it consists of a nidus of tangled arrays of partially
mineralized osteoid trabeculae surrounded by dense sclerotic bone.
•Tumor is mainly located at diaphysis of long bones.
• posterior elements of the vertebrae are common site.
Clinical Features:
-Seen commonly between the age of 5-25 yrs
- bone of the lower extermity are more commonly affected; Tibia
- nagging pain, worst at night and relieved by salicylates
- Mild tenderness at the site of the lesions
-palpable swelling if it is superficial
7. Contd….
•Diagnosis:
-Confirmed by X-Ray: tumor is visible aa a zone of sclerosis surrounding
a radiolucent nidus usually less than 1 cm in size.
-CT scan
Treatment:
-Complete excision of the nidus along with the sclerotic bone is done.
- Prognosis is good.
8. Osteoblastoma
• It is a benign tumor consisting of vascular osteoid and new bone.
• It occurs in the jaw and the spine.
• If in long bones, it occurs in the diaphysis or metaphysis, but never in
the epiphysis.
• It occurs in patients in their 2nd decade of life.
•The patients with aching pain.
• Radiologically, it is a well-defined radiolucent expansible bone lesion 2-
12 cm in size.
• There is minimal reactive new bone formation.
• Treatment is by curettage.
9. Chondroblastoma
• It is a cartilaginous tumor containing characteristic multiple calcium
deposit.
• It occurs in young adults and is located around the epiphyseal plate.
• Bones around the knee are commonly affected.
• Radiologically, There is a well- defined lytic lession surrounded by a
zone of sclerosis.
• Are of calcification within the tumor substance give rise to a mottled
appearance.
• Treatment is by curettage and bone grafting.
10. Hemangioma of the bone
• This is the benign tumor of angiomatous origin commonly affecting the
vertebrae and skull.
• It occurs in young adults.
•Common presenting symptoms are persistent pain and features of cord
compression.
• Typically, one of the lumbar vertebrae is affected.
• Radiologically, it appears as loss of horizontal striation and prominence
of vertical striation of the affected vertebral body.
• Treatment is by radiotherapy.
11. Osteoclastoma(GCT)
• Giant cell tumor is a common bone tumor.
• The tumor consist of undifferentiated spindle cells, profusely
interspersed with multi-nucleate giant cell.
• The tumor stroma is highly vascular.
• The tumor is seen commonly in the age group of 20-40 years i.e after
epiphyseal fusion.
•The bone affected commonly are those around the knee and lower end
of the radius.
Clinical Features:-
-Swelling & vague pain
-Pathological fracture
12. Contd……
Examination:-
-Examination reveals a bony swelling
- surface of the swelling is smooth
- limb may be deformed
Diagnosis:-
-Lytic lesion seen in X-ray
-Soap- bubble appearance seen
-No calcification seen within the tumor
13. Contd……
Treatment:-
- Whenever possible, excision of the tumor is the best treatment.
-If excision is not possible then radiotherapy is done.
-Following treatment methods are commonly used:
a. Excision:-
- It is the treatment of choice when the tumor affects a bone whose
removal does not hamper with function e.g., fibula, lower end of
ulna
14. Contd……
b. Excision with reconstruction:-
- When excision of a tumor at some site may result in significant
functional impairment & reconstructed by as follows-
Arthrodesis by the Turn-O- Plasty procedure
Arthrodesis by bridging the gap by double fibula, one taken from
same extremity and other from the opposite leg.
Arthroplasty- Tumor is excised and attempt is made to reconstruct
the joint in some way. It can be carried out using an autograft.
c. Curettage with or without supplemetary procedure:-
- High reoccurrence rate
- Cryotherapy: Liquid nitrogen is used to producea freezing effect and
thus kill the residual cells and thermal burning of the cells by using
cautrization.
16. Osteosarcoma
- It is the second most common and high malignant primary bone
tumor.
- It is defined as a malignant tumor of the mesenchymal cells
characterized by formation of osteoid or bone by the tumor cell.
- It occurs between the age of 15-25 years.
- lower end of femur , upper end of the tibia and upper end of
humerus most common site.
- It looks like greyish white , hard.
- Histologically tumors vary in the richness of the osteoid,
cartilaginous or vascular components.
17. Contd……
Clinical Features:
- Pain is usually the first symptoms soon followed by swelling
- Pain is constant and boring and becomes worse as the swelling
increase in size.
- h/o trauma
- sometime pathological fracture
Examination:
- Swelling at the metaphysis region.
- Shinny with prominent vein seen over the skin
- Margin of swelling are not well defined
- Regional lymphnodes may be enlarged
18. Contd……
Investigation
- X-ray shows the irregular destruction in the metaphysis,
overshadowed by the new bone formation.
- Codman’s triangle: A triangle area of subperiosteal new bone is seen
at the tumor host cortex junction at the ends of the tumor.
- Serum Alkaline Phosphatase
- Biopsy
19. Contd……
Treatment
- Confirmation of the diagnosis
- Evaluation of spread of tumor
- To plan amputation surgery
- Treatment of the tumor
Local Control: surgical ablation, amputation
Radiotherapy
Chemotherapy Immunotherapy
- Portion of the tumor is implanted into a sarcoma survivor and is
removed after 14 days.
20. Contd……
Follow up:
- Checked up every 6-8 wks
- Any evidence of recurrence of the primary tumor.
Prognosis:
- Without treatment death occurs within 2 yrs, usually within 6 month
of detection of metastasis.
- 5 yrs survival with surgery alone is 20%
- With surgery and adjuvant therapy, 5 yrs survival is 70%