Physical Address
304 North Cardinal St.
Dorchester Center, MA 02124
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
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
Become a Clinical Tree membership for Full access and enjoy Unlimited articles
If you are a member. Log in here