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BONE TUMORS
•General considerations
Malignant bone tumor :
•Paget’s Disease
•Neuroblastoma Giant Cell Tumor •Fibrous Dysplasia
•Neurofibromatosis
Primary benign bone (Ollier’s disease)
Primary •Extraosseous
tumors : •Maffucci’s
malignant bone Osteosarcoma
Syndrome
tumors : •Chondrosarcoma
•Solitary •Periosteal
•Ewing’s sarcoma
osteochondroma Chondroma
•Multiple •Fibrosarcoma
•Hereditary Multiple •Chondroblastoma
Myeloma •Chordoma
Exostosis •Chondromyxoid
•Solitary •Non-Hodgkin’s
•Hemangioma Fibroma
Plasmacytoma Lymphoma of
•Osteoma •Fibrous Xanthoma
•Central Bone
•Gardner’s Syndrome of Bone: Non-
Osteosarcoma •Hodgkin’s
•Bone Island ossifying Fibroma
•Multicentric Lymphoma of
•Osteoid Osteoma •Fibrous Xanthoma
Osteosarcoma Bone
•Osteoblastoma of Bone : Fibrous
•Parosteal •Synovial
•Solitary Cortical Defects
Osteosarcoma Sarcoma
Enchondroma •Simple Bone Cyst
•Secondary •Adamantinoma
•Multiple •Intraosseous Lipoma
Osteosarcoma
Enchondromatosis
BONE TUMORS
The majority of tumors involving bone
are secondary (or metastatic):
- secondary (metastases) (95%)
- primary (5%)
Osteosarcoma is the most common primary
malignant tumor of bone (35%), followed by
chondrosarcoma (25%) and Ewing sarcoma
(16%).
BONE TUMORS
DIAGNOSIS
BONE TUMORS
PATIENT AGE
LOCATION
LOCATION
MATRIX
Opacity
•Margin
•Periosteal Reaction
•Cortical Involvement
Lesion
MARGIN
A focal discrete lesion is called “geographic.”
Geographic lesions are classified as type 1 :
Type 1a (well-defined border with sclerotic rim)
Type 1b (well-defined border but without sclerotic rim)
Solid / unilamellated
Non-aggressive
appearance
The underlying lesion is
slow growing and is
giving the bone a chance
to wall the lesion off.
PERIOSTEAL REACTION
Intermediate
aggressive process
PERIOSTEAL REACTION
Codman triangle
PERIOSTEAL REACTION
PERIOSTEAL REACTION
OPACITY AND MINERALIZATION
Opacity
Bone-forming
Fluffy, amorphous, cloudlike
mineralization
OPACITY AND MINERALIZATION
CHONDRAL MINERALIZATION
Chondral tissue
Punctate, flocculent, comma
shaped, arclike / ringlike
Enchondroma, Chondrosarcoma,
Chondroblastoma
SIZE AND NUMBER
Benign < 6 cm
Malignant > 6 cm
1Osteoid
– 2 cm Chondral
osteoma: lesion
< 1.5 incmlong bone : Enchondroma
>Osteoblastoma
4 – 5 cm : Low-grade
: > 1.5chondrosarcoma
cm
Cortex
Erosion of the inner surface of the cortex endosteal
scalloping
Completely destroyed and breached by the lesion.
Ballooning of the cortex (normal thickness/thin)
CORTICAL INVOLVEMENT
Processes in the medullary canal / the periosteum /
surrounding soft tissue
saucerization
Slowly growing intramedullary process aggressive &
break through an area of solid periosteal reaction
SOFT-TISSUE COMPONENT
Bone lesion + Soft tissue component MALIGNANT process
1. The tumor destroyed the cortex as it expanded, or
2. Permeated through the haversian canals of the cortex to reach the
surrounding tissue.
Osteoid
Brodie’s Abcess
Osteoma
10
Paget’s D
10
10
Age : 13
Location : Metadiaphysis
Margin : 1A – 1B
PX : None
Matrix : None
DX : UBC
ABC
Adult
Metaphysis
Margin 1B
Px None
Matrix None
Age : 66 th
Location : Diaphyseal
Margin : 1A
Px : Minimal , thick
Matrix : None
Dx : WAIT
Age : 66 th
Location : Diaphyseal
Margin : 1A
Px : None
Matrix : None
Dx : WAIT
Age : 66 th
Location :
Diaphyseal
Margin : 1A
Px : None
Matrix : None
DX : MYELOMA
CONCLUSION
Despite the availability of advanced imaging methods such as CT and
MR imaging, the diagnosis of a tumor or tumorlike lesion of bone still
depends on the conventional radiograph.