Poorly differentiated chordoma |
Poorly visualized. May be lytic, destructive bone-based lesion. |
Variable. Usually lytic and destructive bone-based lesion, with surrounding soft tissue component.
Enhancement pattern: Soft tissue component may or may not enhance.
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Classical chordoma |
Poorly visualized. Expansile, lobulated lytic bone-based lesion. |
Bone based lytic mass usually at the skull base or sacrum. Expansile soft tissue mass. Heterogeneous in their attenuation due to interspersing of tumor tissue (isoattenuating) and myxoid cyst or necrotic degeneration (hypoattenuating). Hyperattenuation may correspond to bony sequestration from destruction of bone rather than tumoral calcification.
Enhancement pattern: variable.
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Benign notochordal cell tumors |
Usually not seen. May present as a sclerotic medullary based lesion. |
May be occult on imaging.
Mild to marked sclerosis, usually a vertebral body.
Enhancement pattern: no enhancement.
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Ecchordosis physaliphora |
Poorly visualized. |
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Chondrosarcoma |
Mixed sclerotic and lytic. Chondroid “rings and arcs” matrix. May have aggressive features. Expansile with periosteal reaction and soft tissue component. |
Aggressive, lytic and expansile mass with endosteal scalloping, and soft tissue component. internal “rings and arcs” mineralization.
Enhancement pattern: heterogenous enhancement.
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Metastasis |
Poorly characterized. Variable in appearance, lytic to sclerotic. |
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T1: usually hypo to iso-intense.
T2: Usually T2 hyperintense relative to normal bone
Enhancement pattern: variable
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