Joseph Junewick, MD FACR
over 6 years ago
Please choose a workflow. A standard workflow allows you to browse the repository with full case detail; the academic workflow allows you to browse the repository with limited case detail revealed. Double click on the images to launch image viewer.
Heather Borders, MD
|Diagnostic Category: Neoplasia Benign
|Created: over 7 years ago
|Updated: over 7 years ago
13 year old female with headaches.
Large cystic mass with an enhancing peripheral nodule. Nodule is isointense to gray matter on T1 and T2. Cystic portion is isointense to CSF. No significant surrounding edema. Mild midline shift and mass effect.
Pleomorphic xanthoastrocytoma is a rare, usually benign, cortical-based mass that often enhances intensely with contrast material. Typically a peripheral mass with a cortically based nodule.
The most common location is in the temporal lobes (Temporal>parietal>frontal). Nearly all are supratentorial. Seizures and headaches are common clinical features. Familiarity with this lesion is important in the differential diagnosis of enhancing cortical-based masses.
Differential diagnosis includes, ganglioglioma, JPA, low grade glioma, oligodendroglioma.
T1=nodule isointense to gray matter or mildly heterogeneous, cystic portion is isointense to CSF
T2=nodule hyperintense to minimally heterogeneous, usually an absence of surrounding edema, cystic portion is isointense to CSF
Post-contrast=intense enhancement of the nodule, possibly adjacent meningeal enhancement +/-dural tail
Treatment is surgical. Recurrence is rare, but if it happens, repeat surgery is the treatment.
Stat dx pxa. Karen Salzman.