Intracranial Tumors
Tumor Location
The differential diagnosis for an intracranial mass is dependent on a number of different factors. One of the most important is location. If the mass is extra-axial - outside of the brain parenchyma- it most likely represents a Meningioma if it is dural based or Schwannoma if it is associated with a cranial nerve. If the mass is intra-axial - inside of the brain parenchyma- it could represent a primary tumor, metastatic disease or a tumor mimic.
Glial Tumor Markers
Tumors historically have been classified based on histology and cell of origin. In 2007, there was a paradigm shift, such that genetic markers were applied to preexisting categories to aid in prognosis.
In 2016, CNS WHO classification system was released which incorporates molecular parameters for classification and prognosis.
The primary glial markers are listed in the adjacent table which highlights which profile portends a more favorable/less favorable outcome.
IDH Wildtype Glioblastoma (GR 4)
Location: Most supratentorial
Imaging Features:
Variable enhancement pattern: thick rim, solid, patchy nodular; Heterogenous, can have cysts, necrosis, hemorrhage, calcium rare
High cerebral blood volume on perfusion
Hypercellular elements T2 hypointense, restrict diffusion
Diffuse Astrocytoma IDH Mutant (GR 4)
Location: Most supratentorial
Imaging Features:
Variable enhancement pattern: thick rim, solid, patchy nodular; Heterogenous, can have cysts, necrosis, hemorrhage, calcium rare
High cerebral blood volume on perfusion
Hypercellular elements T2 hypointense, restrict diffusion
Diffuse Astrocytoma IDH Mutant (GR 3)
Location: Two thirds are supratentorial, most frontal/temporal
Imaging Features:
Often indistinguishable from Grade 2 tumors.
Ill-defined T2/FLAIR hyperintense expansile white matter lesion
Grade 3, more heterogeneous, can enhance
elevated relative CBV compared to grade 2 tumors
Diffuse Astrocytoma IDH Mutant (GR 2)
Location: Two thirds are supratentorial, most frontal/temporal
Imaging Features:
Ill-defined T2/FLAIR hyperintense expansile white matter lesion
Grade II, more homogeneous, unlikely to enhance
relatively lower CBV compared to grade 2 tumors.
Pilocytic Astrocytoma (GR 1)
Location: Most often occurs in the posterior fossa, can occur in the optic chiasm/hypothalamus
Imaging Features:
Cyst with an enhancing mural nodule
Favorable prognosis
No diffusion restriction
Oligodendroglioma
Location: 80% supratentorial, most frontal
Imaging Features:
T2/FLAIR hyperintense expansile white matter lesion
Heterogenous, can calcify, have cysts, and enhance (50%)
Prominent enhancement, hemorrhage or necrosis? more likely to be anaplastic/high grade
Lymphoma
CNS Lymphoma can be Primary or Secondary
Location: Periventricular
Imaging Features
Smooth margins, enhancing
Dark on T2, diffusion restricting related to high cellularity
Lymphoma
Secondary CNS lymphoma exhibit similar imaging features as primary CNS lymphoma. The primary difference is that they have disease outside of the CNS.
Intra-Axial
Posterior Fossa Mass
Pilocytic Astrocytoma (Gr 1)
Epidemiology: Occurs in 1st 2 decades
94% survival at 10 yrs;
Most common pediatric CNS glial neoplasm
Symptoms related to mass effect
Location: Cerebellum, ON, Hypothalamus
Imaging Features: “Cyst with enhancing mural nodule”
Medulloblastoma (Gr 4)
Grade: WHO grade 4 (4 subtypes)
Epidemiology: Most common posterior fossa mass in children
Location:
Arise from the vermis and grow into the 4th ventricle
Can be hemispheric
Imaging Features:
Enhancing tumors, dark on T2 and diffusion restricting arising from the roof of the 4th ventricle
Image the spine, drop metastasis may be present.
Ependymoma (Gr 2)
Grade: WHO Grade 2
Epidemiology: bimodal age peaks
Pathology: Glial tumor derived from differentiated ependymal cells that line the ventricles and central canal
Location: Floor of the 4th ventricle
Imaging Features:
Soft malleable appearance, solid, calcification is common (40-80%); Variable enhancement
Subarachnoid spread less common than medulloblastoma- but when present likely reflects higher grade tumor
Hemangioblastoma
Pathology: Rare, benign tumors of vascular origin
Epidemiology: More common in adults, uncommon in children- but can be seen, association with VHL
Location: Occur more commonly in cerebellum
Imaging Features:
Cyst with vascular mural nodule- look for adjacent vessels
Hemorrhage may be present
Extra-Axial
Meningioma
Pathology: benign tumors of nerve origin
Location: Can occur anywhere along the dura
Imaging Features:
Enhancing masses associated with the dura, may have dural tail
Calcification is a common feature
Schwannoma
Pathology: benign tumors of nerve origin
Location: Occur more commonly in the internal auditory canal
Imaging Features:
Enhancing masses involving nerves, most often seen involving CN8