Focal Cortical Mass
James D. Eastwood, MD
DIFFERENTIAL DIAGNOSIS
Common
Cerebral Ischemia-Infarction, Acute (Cortical)
Metastases, Parenchymal
Oligodendroglioma
Cerebritis
Diffuse Astrocytoma, Low Grade
Less Common
Venous Infarction
Pleomorphic Xanthoastrocytoma
Tuberous Sclerosis Complex
Pachygyria-Polymicrogyria (Focal Cortical Dysplasia)
DNET
Ganglioglioma
Rare but Important
Pilocytic Astrocytoma
Cavernous Malformation
Desmoplastic Infantile Ganglioglioma
Viral Encephalitis
Astroblastoma
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Is the mass enhancing or not?
Is there vasogenic edema?
Does part or all the mass contain low ADC values?
Is the lesion solitary or multiple?
Are bilateral lesions present?
Lesions in this differential are primarily related to tumor, ischemia, & infection
Helpful Clues for Common Diagnoses
Cerebral Ischemia-Infarction, Acute (Cortical)
Often wedge-shaped, involve both gray & white matter (WM)
Bright on T2, FLAIR, & DWI with low ADC values
Typically seen in vascular territories
Usually a unilateral process; can be bilateral when there is a central source of multiple emboli (i.e., cardiac disease)
Metastases, Parenchymal
Often occur at gray-white junctions
Enhancing mass with surrounding vasogenic edema
Usually solid, may be complex with central cystic or necrotic areas
May be hemorrhagic with increased T1 SI
May be solitary but frequently are multiple & bilateral
Oligodendroglioma
T2 hyperintense mass, variable enhancement
Calcification is common
Frontal > other lobes; usually a single mass
Cerebritis
Gray & white matter are often involved together
T2 hyperintense with variable enhancement & variable DWI appearance
Cerebritis essentially represents a developing brain abscess & is commonly caused by pyogenic bacteria
May be solitary or multifocal
Diffuse Astrocytoma, Low Grade
T2 hyperintense WM mass, may involve gray matter
May mimic stroke; however ADC values typically normal to elevated
No or minimal enhancement is typical
Usually a solitary mass
Bilateral disease may be seen in gliomatosis cerebri, a rare infiltrative process
Helpful Clues for Less Common Diagnoses
Venous Infarction
T2 hyperintense lesion
Associated hemorrhage is very common, often at gray-white junctions
Typically related to dural sinus thrombosis
May be multiple & bilateral if the superior sagittal sinus is involved
Pleomorphic Xanthoastrocytoma
Cortical enhancing mass with adjacent cyst, classic appearance
Enhancement extends to meninges, causing a “dural tail”
Temporal lobe is most common location
Occurs in young adults
Tuberous Sclerosis Complex
Multiple cortical “tubers” = cortical hamartomas are T2 hyperintense & nonenhancing
Calcified subependymal nodules ± enhancing giant cell astrocytoma at the foramen of Monro is classic
Usually a multiple & bilateral process
When solitary, consider Taylor cortical dysplasia
Pachygyria-Polymicrogyria (Focal Cortical Dysplasia)
Limited to gray matter; focal or regional thickening of the cortex
Variable T2 appearance; no enhancement
Many have deep sulci with thickened cortex that mimics a mass
Occasionally a linear region of increased T2 signal connects the focal cortical dysplasia with the ependymal surface
DNET
Multicystic cortical mass, frequently seen in the temporal lobe
“Bubbly” appearance classic
Variable enhancement
Solitary lesion in a young adult typical
Ganglioglioma
Enhancing (multi)cystic mass; may be solid or have a cyst & nodule appearance
Calcification is common
Temporal lobe is most common location
Solitary lesion
Helpful Clues for Rare Diagnoses
Pilocytic Astrocytoma
Enhancing nodule with or without an associated cyst, most common appearance
Children > adults
Cerebellum & optic pathways are frequent locations
May rarely occur in the cortex
Solitary lesion
Cavernous Malformation
Heterogeneous mass with a “mulberry” appearance related to blood products
Hemosiderin ring “blooms” on GRE; T1 bright locules
May have increased CT density &/or punctate calcifications
Sometimes associated with a developmental venous anomaly
May be deep as well as cortical
May be solitary or multiple, bilateral
Desmoplastic Infantile Ganglioglioma
Frontal/parietal locations common
Cystic mass with enhancement
May be massive, occupy majority of hemisphere
Presentation occurs when younger than 6 months
Viral Encephalitis
Cortical swelling; minimal enhancement
Not in a typical vascular territory
Temporal, frontal, cingulum are often seen in herpes simplex virus
Astroblastoma
Large hemispheric solid & cystic mass with heterogeneous enhancement of solid portionStay updated, free articles. Join our Telegram channel
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