Astrocytoma

Case contributed by Frank Gaillard
Diagnosis certain

Presentation

Seizure.

Patient Data

Age: 30 years
Gender: Male
mri

Right frontal lesion has 2 components:a nodular component medially that has herniated beneath the falx to cross midline with multiple small vessels and wispy enhancement, and a crescentic lateral component that demonstrates the T2 FLAIR mismatch sign. There is additional surrounding peritumoural oedema. The lesion appears intra-axial and solitary. Local mass effect has compressed the right frontal horn and created a midline shift of 1 cm and has displaced the 2 A2 branches (in close proximity to its left posterior margin)

Case Discussion

 

The patient went on to have a resection. 

Histology

Sections of cerebellar cortex and white matter show a cellular tumour with a loose fibrillary background. Tumour cells have ovoid to angulated hyperchromatic nuclei with some gemistocytic cells. Mitoses are rare with up to 1 per 50 HPF within the most cellular areas. Necrosis and microvascular proliferation are not present.

Immunohistochemistry:

  • GFAP: Positive
  • OLIG2: Positive
  • IDH-1 R132H: Positive (mutated)
  • ATRX: Lost (mutated - implies intact (not deleted) 1p19q status)
  • p53: Positive
  • p16 CDKN2A: Patchy
  • Ki67: Less than 5%

FINAL DIAGNOSIS: diffuse astrocytoma, IDH-mutant (WHO Grade II).

Discussion

Although the grade histologically is only WHO grade II, the presence of enhancement and lower ADC values are concerning for a higher grade component. Depending on how much of the tumour has been sent to pathology and which parts were examined there is always the risk of under-grading. 

How to use cases

You can use Radiopaedia cases in a variety of ways to help you learn and teach.

Creating your own cases is easy.

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.