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Primary neoplasm of astrocytic origin within spinal cord
Fusiform expansion of cord with enhancing component of variable morphology
Almost always enhances
Cervical > thoracic
Usually ≤ 4 segments
Occasionally multisegmental, even holocord (more common with pilocytic astrocytoma)
± cyst/syrinx (fluid slightly T1 hyperintense to cerebrospinal fluid)
Hyperintense on proton density and T2WI MR
Myelopathy should be evaluated with contrast-enhanced MR
Ependymoma
Hemangioblastoma
Syringohydromyelia
Autoimmune or inflammatory myelitis
80-90% low grade
10-15% high grade
Slow onset of myelopathy
May cause painful scoliosis
Most are slow growing
Malignant tumors may cause rapid neurologic deterioration
Most common intramedullary tumor in children and young adults
Overall, ependymomas > astrocytomas (2:1)
Myelopathy should be evaluated with MR
with a rostral cystic cord component
.
. The tumor subtype and histological grade are the most important prognostic factors. Malignant transformation, although common in recurrent adult low-grade gliomas, is unusual in pediatric low-grade intramedullary spinal cord tumors.
. Astrocytomas tend to have an eccentric growth pattern and are T2 hyperintense. Up to 1/3 are reportedly nonenhancing but have mass effect and cord expansion.
within the central spinal canal in this case of cervical spinal cord astrocytoma with holocord edema (not shown).
Intramedullary glioma
Primary neoplasm of astrocytic origin within spinal cord (SC)
Best diagnostic clue
Enhancing infiltrating mass expanding SC
Location
Cervical > thoracic
Size
Usually ≤ 4 segments
May be extensive, especially with pilocytic histology
Morphology
Fusiform spinal expansion, with enhancing component of variable morphology
Occasionally asymmetric, even exophytic
Eccentric > central growth pattern
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