• Well-differentiated, slowly growing neuroepithelial tumor
composed of neoplastic ganglion cells and neoplastic glial
• Most common neoplastic cause of temporal lobe epilepsy
• Best diagnostic clue: Partially cystic, enhancing, cortically
based mass in child/young adult with TLE
• Can occur anywhere, but most commonly superficial
hemispheres, temporal lobe (> 75%)
• Circumscribed cyst with mural nodule most common
• May be solid and appear well circumscribed
• Calcification is common (up to 50%)
• Superficial lesions may expand cortex, remodel bone
• Protocol advice: Contrast-enhanced MR to include coronal
T2 images for better evaluation of temporal lobes
• Pleomorphic xanthoastrocytoma
• Dysembryoplastic neuroepithelial tumor
• WHO grade I or II (80% grade I)
• Uncommon: Anaplastic ganglioglioma (WHO III)
• Rare: Malignant with glioblastoma multiforme-like glial
• Occurs at all ages (peak: 10-20 years)
• Most common mixed neuronal-glial tumor
• Cortical dysplasia is commonly associated with
• Excellent prognosis if surgical resection complete
(Left) Coronal graphic shows a
the overlying cortex. Calvarial
remodeling is seen, typical of a
temporal lobe epilepsy. (Right)
circumscribed, cystic, and solid
partially calcified frontal lobe
Calcification is seen in 30-50%
differential diagnosis for this
No comments:
Post a Comment
اكتب تعليق حول الموضوع