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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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| 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 |
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 |
| 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 |
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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 |