Spinal cord glioblastoma

Case contributed by Yune Kwong
Diagnosis certain

Presentation

3-month history of urinary difficulties culminating in acute admission with urinary and fecal incontinence.

Patient Data

Age: 60 years
Gender: Male

MRI Total spine

mri

T2 images show a hyperintense lesion in the conus, with slight expansion. This enhances following contrast administration. The intense solid-like enhancement does not favor demyelination or other inflammatory disorder. A tumor such as ependymoma was considered at the time of imaging.

1mth later post steroids

mri

On this follow up scan, the conus is even more hyperintense and expanded. The area of enhancement has also increased, and note the increased vascularity of the pial vessels leading up to the lesion. On the axials, a small non-enchancing necrotic area has developed on the right side of the lesion. New enhancement of the cauda roots is also seen, suggesting leptomeningeal dissemination.

An interesting associated finding is thoracic epidural lipomatosis secondary to the high dose steroids. The proliferation of epidural fat dorsal to the thoracic cord causes the CSF anterior to the cord to be effaced (compare with original study).

Case Discussion

The appearances following the second scan were strongly in favor of an intrinsic cord tumor (CT body was negative). The patient went for a debulking, and the histology showed glioblastoma (GBM). This is an example of a common tumor in an uncommon location. In retrospect, the imaging findings were all those expected for a GBM if seen in the brain.

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