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Spinal ependymomas are slow-growing intramedullary tumors arising from ependymal cells lining the central canal of the spinal cord.

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Epidemiology


Feature Details
Age group Adults (30–50 years)
Sex No significant gender predilection
Incidence Most common spinal cord tumor in adults (~60% of intramedullary tumors)
Pediatric counterpart Less common in children compared to astrocytomas

Classification


WHO classification:

Grade Subtype Characteristics
Grade I Found in conus medullaris, filum terminale, or cauda equina
Grade II Classic ependymoma Most common spinal form
Grade III Anaplastic ependymoma Rare, aggressive, seen in pediatric patients

Common locations:

Location Details
Cervical spine Most frequent in adults
Thoracic spine Second most common
Conus medullaris/filum terminale Typical site for myxopapillary subtype
Central canal Originates from ependymal lining

Clinical features


Symptoms Mechanism
Back or radicular pain Local tumor irritation or nerve root compression
Motor weakness UMN signs if intramedullary
Sensory loss Dissociated sensory level, paresthesia
Bowel/bladder dysfunction Especially if lesion in conus
Gait disturbance Due to long tract involvement

Radiology


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Typically centrally located well-defined lesion with associated features such as Hemosiderin cap sign and polar cystic dilatation (syringohydromyelia)

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MR sequence Imaging features
T1 Iso- to hypointense
• May show intratumoral hemorrhage (hyperintense foci)
T2 Hyperintense, centrally located lesion with cord expansion
• Often spans 3–5 vertebral levels
• Associated rostral and caudal polar cysts are common
Contrast Strong and homogeneous enhancement (classic)
• May be heterogeneous if hemorrhage or necrosis is present
GRE/SWI Shows blooming due to hemosiderin (cap sign) — a classic feature