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Subcutaneous Leiomyosarcoma
Joseph Junewick, MD FACR
over 10 years ago
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Ganglioglioma - Spinal Cord

Case Detail

Anatomy: Brain-Spine
Joseph Junewick, MD FACR
Diagnostic Category: Neoplasia Malignant
Created: over 9 years ago
Updated: over 9 years ago
Tags: PEDS
Modality/Study Types: MR
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1 year old male with developmental regression.

Case Images


Ganglioglioma – Spinal Cord


MR – Sagittal T2 and post-gadolinium T1 images of the spine show a long segment of cord expansion from the pontomedullary junction to the mid-thoracic cord related to patchy enhancing neoplasm and marked vasogenic edema.


Ganglioglioma is a rare CNS tumor (~1% of CNS tumors). Gangliogliomas are composed of a mixture of neoplastic neuronal or ganglion and glial (usually astrocytic) cells; classification is based on the degree of differentiation of the neuronal or ganglion cells. Gangliogliomas are slow growing relatively benign tumors but have a recurrence rate of nearly 50%. Of totally resected spinal cord tumors, low-grade astrocytoma is most common followed by ganglioglioma and then ependymoma and high-grade astrocytoma. Gangliogliomas are associated with long segment or holocord involvement, reactive and tumoral cysts, scoliosis and bony remodeling.


Patel U, Pinto RS, Miller DC, et al. MR of spinal cord gangliogliomas. AJNR (1998); 19: 879-887.

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