There is a hypointense lesion on the T1 Weighted images in the upper shaft of the right tibia in the metaphysis and also involving the region of the epiphysis posteriorly and extending up to the knee joint. This lesion is seen to turn heterogeneously hyperintense on the proton density and STIR images. This lesion is seen to extend over 10 cms from the level of the knee joint. There is a clear zone of transition between the normal marrow and the lesion.
Osteosarcoma is the most common primary malignant bone tumor in
childhood. The identifying feature of all osteosarcomas is the presence of
malignant stromal cells that produce osteoid. There are two main categories of
osteosarcoma, primary (de novo) and secondary.
PRIMARY OSTEOSARCOMA:
They often affect individuals younger than 20 years of age with a slight
predominance in male patients. The lesion is usually metaphyseal and involves
long bones It destroys trabecular and cortical bone, invades the soft tissues
and may extend into the epiphysis.
SECONDARY OSTEOSARCOMA:
It arises in a setting of preexisting bone disease (e.g., Paget’ s disease, bone
infarcts) or after exposure to irradiation . In osteosarcoma associated with
Paget’ s disease, bones other than the long bones (e.g., the pelvis, skull,
facial bones and scapula) are involved.
Pathology:
Several pathologic patterns of osteosarcomas have been identified.
Telangiectatic
osteosarcomas:
They show hemorrhage and necrosis and may simulate an aneurysmal bone cyst. On
conventional radiographs, the telangiectatic variant appears lytic because of
the lack of demonstrable bone production. MRI shows an aggressive, destructive
lesion, usually accompanied by an associated soft-tissue mass. The inhomogeneity
of signal intensity, with both low and high signal intensity areas on T1W and
T2W images, reflects the high degree of vascularity and the presence of large
hemorrhagic cystic spaces.
Osteoblastic
osteosarcoma:
They are rich in bone production and the bone and osteoid are deposited in
massive solid amounts. The mineralization extends into the soft tissues. Blastic
components remain low in signal intensity on T1W and T2W images, but associated
peritumoral edema or nonsclerotic areas show increased signal intensity on T2W
or STIR images.
Chondroblastic
osteosarcoma:
The generation of chondroid elements, whether benign or malignant, contributes
to increased signal intensity on T2-weighted images.
Fibroblastic
osteosarcoma:
Osteosarcomas that produce large amounts of spindly fibroblasts
are classified as fibroblastic osteosarcoma.
Central, low-grade
osteosarcoma:
It is a rare type of osteosarcoma arising in medullary bone and is so well
differentiated that it is frequently mistaken for a benign condition both
radiologically and histopathologically. The lesion appears well circumscribed,
simulating fibrous dysplasia. A search for small foci of cortical destruction
may be essential for accurate diagnosis. The prognosis is excellent.
Metastasis occurs late, if ever; but local recurrences may be a serious problem
if surgery is inadequate. On MRI, the low-grade central osteosarcoma may be
difficult to distinguish from a conventional osteosarcoma, which has an
identical radiographic appearance.
Juxtacortical
osteosarcomas:
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Periosteal osteosarcoma:
It favors the diaphyseal surface of long tubular bones and forms an irregular
thickened cortex. Histologically, hyaline chondrosarcomatous elements are a
prominent feature.
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Parosteal osteosarcoma:
They occur most frequently on the metaphyseal surface of long tubular bones
within the parosteal soft tissue, and forms a lobulated mass. Histologically it
is characterized by a fibrous proliferation surrounding parallel lamellar bony
spicules. The fibrous component can appear externally bland, mimicking a fibrous
dysplasia. Unlike periosteal osteosarcomas, chondrosarcomatous elements are
minimal or absent in parosteal osteosarcomas. MR imaging performed in the early
stages of developing myositis ossificans may display changes, which can be
mistaken for a more aggressive process, such as parosteal or periosteal
osteosarcoma. Rim enhancement with intravenous contrast injection and
hyperintensity on T2W images mimics the appearance of an abscess or necrotic
tumor.
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High-grade surface osteosarcoma:
MRI:
The distal femur, proximal tibia, and humerus are common sites of involvement in
conventional osteosarcoma. With MRI, intramedullary marrow involvement,
soft-tissue extension, skip-lesion metastases and postoperative recurrence can
be accurately assessed. Marrow infiltration can be mapped on MRI, even when
standard radiographic results are negative. MRI can be used to differentiate
exuberant bone, which is isointense with yellow marrow, from osteosarcoma, which
causes both T1 and T2 prolongation. In addition, MR scans of aggressive,
dedifferentiated osteosarcomas may demonstrate a necrotic, hemorrhagic
fluid-fluid level within the more distal marrow cavity.
Osteosarcomas tend to demonstrate low signal intensity on T1Wsequences and high
signal intensity on T2W sequences. Specific cellular constituents (e.g.,
fibrous, chondroid, blastic or telangiectatic components), however, can modify
signal characteristics.
There is excellent correlation between the MR appearance of the extent of
marrow, cortical bone and soft-tissue involvement and the gross pathologic
specimen. Lesions that are primarily blastic and therefore sclerotic on plain
film radiographs, demonstrate low signal intensity on both T1W and T2W
sequences. However, even in lesions with extensive sclerosis, areas of increased
signal intensity may be identified on T2W images. Hemorrhagic components within
telangiectatic osteosarcoma demonstrate focal areas of high signal intensity on
T1W and T2Wimages. Skip lesions and multiple sites of involvement are common in
multicentric osteosarcoma.
In cases of parosteal osteosarcoma, the precise involvement of cortex and marrow
can be assessed using sagittal or coronal images. Both edema and tumor extension
may encase vessels and multiple axial images are usually necessary to
distinguish edema that conforms and tracks along specific muscle groups.
1. A dark pattern of low to intermediate signal intensity areas on T1W and T2W
images may correspond to calcified osteoid or cartilage matrix, dense
granulation tissue and hemosiderin
2. A mottled or speckled pattern of intermediate signal intensity on T1W images
and high signal intensity on T2W images, best appreciated on T2-weighted images
may correspond to tumor matrix, edematous granulation tissue and hemosiderin
deposits
3. A multicystic or bubbly appearance in the cystic pattern, of intermediate to
high signal intensity on T1W images and high signal intensity on T2Wimages, is
thought to correspond to either blood-filled cysts with viable tumor cells or
tumor matrix mixed with edematous granulation tissue; however, foci of residual
viable tumor cannot be specifically diagnosed
4. Skip metastases, a reduction in peritumoral edema, the development of a dark
rim of collagenous capsule continuous with the periosteum, bone infarcts and
intramedullary vascular channels can all be identified.
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