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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.
WHO Nomenclature & Classifications
1 Bone forming tumors
Benign Osteoid osteoma, osteoma, Osteoblastoma
Indeterminate Aggressive osteoblastoma
Malignant Osteosarcoma
2 Cartilage forming tumors
Benign Osteochondroma, Chondroblastoma,
Malignant Chondrosarcoma
3 Gaint cell tumor(Osteoclastoma)
4 Marrow tumor
primary tumor commonest Multiple myeloma
5 Vascular tumor
Benign hemangioma
Malignant Angiosarcoma
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.
Treatment
•No treatment is generally required except for cosmetic reasons.
• Simple excision is sufficient.
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
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.
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.
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.
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.
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
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
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
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.
Contd……
d. Amputation:-
e. Radiotherapy:-
- It is preferred treatment for GCT affecting the vertebrae
Prognosis:
- Recurrence is more common.
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.
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
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
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.
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%
THANK YOU

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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.
  • 3. WHO Nomenclature & Classifications 1 Bone forming tumors Benign Osteoid osteoma, osteoma, Osteoblastoma Indeterminate Aggressive osteoblastoma Malignant Osteosarcoma 2 Cartilage forming tumors Benign Osteochondroma, Chondroblastoma, Malignant Chondrosarcoma 3 Gaint cell tumor(Osteoclastoma) 4 Marrow tumor primary tumor commonest Multiple myeloma 5 Vascular tumor Benign hemangioma Malignant Angiosarcoma
  • 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.
  • 15. Contd…… d. Amputation:- e. Radiotherapy:- - It is preferred treatment for GCT affecting the vertebrae Prognosis: - Recurrence is more common.
  • 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%